Joseph Gaudio, M.D.; Suspension of Registration, 10083-10095 [E9-4903]
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hereby is, granted, subject to the
conditions set forth above. This Order is
effective immediately.
Dated: February 26, 2009.
Michele M. Leonhart,
Deputy Administrator.
[FR Doc. E9–4906 Filed 3–6–09; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. 06–28]
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Joseph Gaudio, M.D.; Suspension of
Registration
On September 16, 2005, the Deputy
Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration, issued an Order to
Show Cause to Joseph Gaudio, M.D.
(Respondent) of Alpine, New Jersey.
The Show Cause Order sought the
revocation of Respondent’s DEA
Certificate of Registration, which
authorizes him to handle controlled
substances as a practitioner, and the
denial of any pending applications to
renew or modify his registration, on the
ground that he had committed acts
which rendered his continued
registration ‘‘inconsistent with the
public interest.’’ Show Cause Order at 1
(citing 21 U.S.C. 823(f) & 824(a)(4)).
The Show Cause Order alleged that
Respondent had issued prescriptions for
controlled substances which lacked a
legitimate medical purpose, and that in
doing so, he had acted outside of the
usual course of professional practice. Id.
at 1 & 6. The Show Cause Order
specifically alleged that Respondent had
‘‘prescrib[ed] controlled substances to
Internet customers despite never
establishing a genuine doctor-patient
relationship with the Internet
customer.’’ Id. at 5. Relatedly, the Show
Cause Order alleged that Respondent
‘‘did not see customers, had no prior
doctor-patient relationships with the
Internet customers, did not conduct
physical exams, * * * did [not] create
or maintain patient records,’’ and that
‘‘[t]he only information usually
reviewed prior to issuing drug orders
was the customer’s online
questionnaire.’’ Id. at 6.
The Show Cause Order also alleged
that ‘‘[a] review of prescriptions filled
by [Carrington Healthcare System/
Infiniti Services Group] revealed that
[Respondent] ha[d] issued drug orders
for controlled substances to Internet
customers throughout the United States,
including Georgia, Texas, Pennsylvania,
Alabama, Louisiana, and Kentucky.’’ Id.
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The Show Cause Order further alleged
that ‘‘[a] review of prescriptions filled
by [Carrington/Infiniti] for the period
October 13, 2004 to January 21, 2005,
revealed that [Respondent] ha[d] issued
16 drug orders to Internet customers in
at least nine different states.’’ Id.
On October 21, 2005, Respondent,
through his counsel, requested a hearing
on the allegations. The matter was
assigned to Administrative Law Judge
(ALJ) Gail Randall, who conducted a
hearing on May 2–5, 2006, in New York,
NY. At the hearing, both parties put on
testimony and introduced documentary
evidence. Thereafter, both parties
submitted briefs containing their
proposed findings of fact, conclusions of
law, and arguments.
On November 2, 2007, the ALJ issued
her recommended decision. In her
decision, the ALJ concluded that ‘‘[t]he
Government has clearly demonstrated
that the Respondent’s Internet practice
and his resulting issuance of controlled
substance prescriptions * * * violated
the Controlled Substances Act.’’ ALJ at
43. Applying the totality of the
circumstances test, the ALJ concluded,
however, that the revocation of
Respondent’s registration was not
warranted. Id. at 43–44.
The ALJ specifically noted that
‘‘Respondent’s conduct encompassed a
one year period,’’ that Respondent had
‘‘voluntarily cease[d]’’ his conduct, but
that he had not done so until three
months after he was served with the
Show Cause Order. Id. at 43. While the
ALJ deemed Respondent’s cessation of
his conduct as ‘‘commendable because
of its voluntary nature,’’ she further
explained that he ‘‘demonstrated a lack
of sound judgment’’ in ‘‘continuing to’’
prescribe after being served with the
Show Cause Order. Id. at 44. The ALJ
also found of concern ‘‘Respondent’s
failure to be totally truthful during his
testimony.’’ Id.
The ALJ reasoned, however, that
Respondent was ‘‘a very educated,
dedicated and talented physician
practicing in a sometimes difficult
specialty, pain management,’’ and that
the revocation of his registration would
render him ‘‘being unable to handle
controlled substances’’ in his specialty.
Id. Because the record demonstrated
that Respondent had practiced medicine
for eleven years, and that ‘‘the only
instances of [his] improper handling of
controlled substances were related to
his’’ Internet prescribing, the ALJ
recommended that Respondent’s
registration be continued subject to the
condition that he ‘‘not engage in any
activity involving prescribing controlled
substances and the Internet.’’ Id.
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Having considered the entire record
in this matter, I hereby issued this
Decision and Final Order. I adopt the
ALJ’s conclusions that Respondent
violated both the Controlled Substances
Act (CSA) and various state standards of
medical practice in issuing
prescriptions to persons who ordered
drugs through an Internet site. For
reasons explained below, I reject the
ALJ’s recommended sanction as
inconsistent with agency precedent and
will order the suspension of
Respondent’s registration for a period of
one year. I make the following findings.
Findings
Respondent is a medical doctor who
is board certified in both anesthesiology
and pain management and is licensed to
practice medicine in the States of New
York and New Jersey. Tr. 488.
Respondent is also the holder of a DEA
Certificate of Registration, which
authorizes him to dispense controlled
substances in schedules II through V as
a practitioner. GX 1, at 2. While the
expiration date of Respondent’s
registration was September 30, 2006,
Respondent submitted a renewal
application on August 4, 2006. See
Reply to Respondent’s Status Report, at
1. I therefore find that Respondent’s
prior registration has remained in effect
pending the issuance of this Final Order
and that Respondent also has an
application pending before the Agency.
See 5 U.S.C. 558(c).
Respondent attended medical school
at The Autonomous University of
Guadalajara, and the New York Medical
College. RX 1, at 2. Subsequently,
Respondent did his residency in
anesthesiology at St. Luke’s/Roosevelt
Hospital, an institution which is
affiliated with the Columbia University
College of Physicians and Surgeons,
where he received an award given to the
Outstanding Graduate Resident in
Anesthesiology. Id. Respondent also did
a fellowship in Pain Management at the
Memorial Sloan Kettering Cancer
Center, where he was elected Chief
Fellow. Id. at 1.
Upon completion of his fellowship,
Respondent joined New Jersey
Anesthesia Associates (NJAA), a group
of physicians which provides anesthesia
services at St. Barnabas Medical Center.
Tr. 345–47. Respondent is a partner in
NJAA. Id. at 347. In addition to
providing anesthesia, Respondent also
treats both acute and chronic pain
patients. Id. at 555–56. Respondent is
also an attending physician and clinical
professor at St. Barnabas, where he
trains residents in anesthesia. Id. at 360.
Respondent came to the attention of
the Agency during its investigation of a
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large criminal conspiracy which was
run by Johar Saran, and which used the
Internet to unlawfully distribute
controlled substances. Id. at 156–159;
see also GX 16 (Indictment, United
States v. Saran, et al., No. 305–CR–
0240P (N.D. Tex. 2005). As part of the
investigation, DEA Investigators
conducted trash runs at the premises of
Carrington Health Care System, an
entity owned by Saran which was
located at 301 E. Stephens, Suite 100,
Arlington, Texas. Tr. 159, 185. During
the trash runs, investigators found
various documents including ‘‘Drug
Prescription’’ sheets and copies of some
prescription labels which are placed on
pill vials. See GXs 17–29.
The ‘‘Drug Prescription’’ sheets listed
a patient’s name, address, birth date,
age, sex, phone number, medication
history, and allergies. See GXs 17–24. In
the block titled ‘‘Physician,’’ the sheets
listed Respondent’s name, address,
phone numbers, and DEA number. Id. In
the block titled ‘‘Rx,’’ the sheets gave
the date, drug name (which in each
instance was a schedule III controlled
substance containing hydrocodone),
quantity, number of refills, instructions
for taking the drug, instructions to the
pharmacist as to whether substitution
was permitted or the drug was to be
dispensed as written, and bore the
electronic signature of Respondent. See
id. In a block entitled ‘‘Pharmacy
Services Use Only,’’ each of the sheets
listed a number, as well as the date and
time of a consultation, and included the
notation ‘‘LBRTY.’’ Id. 1 Finally, each of
the sheets included shipping
information. Id.
The prescription labels listed
‘‘Triphasic Pharmacy,’’ with an address
of ‘‘301 E. Stephens St. Ste 100’’ in
Arlington as the dispensing pharmacy.
GXs 25–31. The labels also listed the
patient’s name, the drug, a date, the
quantity dispensed, a prescription
number, instructions for taking the drug,
number of refills, and a physician’s
name. Id. Respondent was listed as the
prescribing physician on eight of the
prescription labels, each of which
indicated that the customer had
received a schedule III controlled
substance containing hydrocodone. See
id.
Several months later, Respondent was
served with the Show Cause Order. Tr.
51–52. When asked by a DI whether he
had prescribed over the Internet,
Respondent admitted that ‘‘he had a
contract with a company called Liberty
1 At the top of all but one of the sheets was the
notation: ‘‘From: Dr. Joseph Gaudio, M.D.,’’ and a
date and time which was typically only a short
period after the date and time listed for the
consultation. See GXs 17, 18, 20, 21, 22, 23.
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Med,’’ that ‘‘he reviewed on-line patient
applications of Liberty Med,’’ and that
he ‘‘was paid $20 per on-line patient
consultation.’’ Id. at 52. Respondent also
told the DI that he reviewed MRIs and
X-rays. When asked if he maintained
patient records, Respondent told the DI
that Liberty Med ‘‘kept them.’’ Id. at 53.
In his testimony, Respondent
explained that in October 2004, one of
his partners in NJAA introduced him to
Liberty Medical and Mr. Craig Boswell,
whose mother ran the company. Tr.
371–72. Respondent’s partner told him
that ‘‘he understood [that Liberty] was a
legitimate company that practices
Internet-based medicine and that I
might be interested in talking to Craig
Boswell concerning possibly doing work
for them.’’ Id. at 371.
Respondent met with Boswell, who
told him that the company ‘‘was not one
of these companies opening and
shutting in a week or month, [that it]
was a legitimate company, [and that]
they wanted to set up consultation
services doing this internet website.’’ Id.
at 373. Boswell further advised
Respondent that Liberty ‘‘deal[t] with
patients who have medical records, who
have been seen by other physicians,
who have radiological evidence of
pain.’’ Id. Boswell also told Respondent
that Liberty would carefully screen the
patients, that ‘‘they would make sure
that the patient wasn’t sourcing meds
from another facility,’’ and that ‘‘they
would also obtain’’ the address and
phone number of the patient’s primary
physician ‘‘so that we could call them
if there is any question as to whether’’
the person was ‘‘a legitimate patient.’’
Id. at 374.
Boswell subsequently asked
Respondent if he would perform on-line
consultations for Liberty. Id. The
consultations were to involve
‘‘interview[ing] the patients’’ and
‘‘mak[ing] a recommendation’’ to
prescribe drugs based ‘‘on all the
information.’’ Id.
In his testimony, Respondent
maintained that he asked Boswell
whether this was permissible. Id. at 375.
Respondent stated that Boswell
‘‘assured [him] that everything was
legitimate,’’ that Boswell told him that
‘‘he was in the Armed Forces,’’ and that
‘‘he had two men in his squad [who]
were in the DEA and [that] he
constantly bounced questions off of
them * * * always to make sure that he
was within the limits of the law.’’ Id.
Boswell also told Respondent that
‘‘there were certain states that did not
allow internet prescribing’’ and that
persons from these states would be
excluded. Id. at 376.
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Respondent did not, however, seek
legal advice regarding the lawfulness of
Boswell’s proposal. Id. at 375.
Moreover, even though he understood
that he would be prescribing to patients
throughout the country, he did not
undertake any inquiry on his own into
the laws of any State pertaining to the
propriety of the proposed activity. Id. at
512. Instead, he concluded that Liberty
was engaged in legitimate activity
because Boswell had been referred to
him by his partner and Boswell was
‘‘concerned about making sure that
everything was done correctly,’’ id. at
375, and had told him that ‘‘he had
reviewed all the laws pertaining to
this.’’ Id. at 512.2
In November 2004, Respondent
entered into a written contract with
Liberty; Respondent performed online
consultations and prescribings for it
from approximately December 2004
through December 2005. Id. at 507.
Respondent was paid $20 per
consultation and received the same fee
regardless of whether he prescribed a
drug.3 Id. at 382–83, 508, 601.
Respondent did consultations for
Liberty five days a week, and did so
every week between December 2004 and
December 2005, except for three weeks
during which he took vacation. Id. at
516. Respondent performed twenty to
fifty consultations a week; he also
testified that while he was ‘‘not exactly
sure,’’ he issued twenty to thirty
prescriptions a week. Id. The record is,
however, unclear as to how many of the
prescriptions were for controlled
substances. Id. at 568.4 According to
2 Respondent also maintained that ‘‘to find out
more’’ he had talked with another physician who
performed online consultations for Liberty. Id. at
509. Respondent did not, however, testify as to the
specifics of this conversation. Id. Respondent did
not meet any of the medical professionals who
worked for Liberty and did not know where the
business was located. Id.
3 Respondent maintained that his compensation
from Liberty was only ‘‘a very small part of [his]
income’’ and that ‘‘it was more of my interest in
telemedicine that drove me to do it.’’ Tr. 383.
Respondent testified that he was involved in a startup company, Technology Integrated for Medical
Application (TIMA), which conducted academic
research with major institutions, and that TIMA
was developing systems to engage in medical
monitoring of people from remote locations. Id. at
505. Respondent explained that ‘‘[w]e can speculate
that some day we’ll be able to diagnose patients
from a distance where you can have a doctor in a
remote location who doesn’t have the expertise in
a certain area that can receive expertise from * * *
physicians in another area based on giving real time
information back to those physicians.’’ Id. at 506.
4 Respondent testified that he prescribed both
narcotics and non-narcotics and that the estimated
number of prescriptions referred to ‘‘all in total.’’
Tr. 568. Notably, the Government introduced no
evidence showing the number of controlledsubstance prescriptions he issued during the course
of his contract with Liberty; nor did it introduce
evidence showing the number of controlled
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Respondent, he prescribed
hydrocodone, Vicodin (a schedule III
controlled substance which contains
hydrocodone), and oxycodone, a
schedule II controlled substance. Id. at
547. See Physicians’ Desk Reference 526
(59th ed. 2005); see also 21 CFR
1308.12(b)(1) & 1308.13(e).
Liberty gave Respondent a user name
and password, which he used to access
PSDOCTOR, a Web-based software
program which listed his appointments;
according to Respondent, he ‘‘would
call the patient and obtain a detailed
history.’’ Id. at 377. Respondent testified
that through PSDOCTOR, he could
retrieve patient records including a
patient’s history (including the patient’s
complaint, what drugs the patient was
taking, what surgeries the patient had
undergone, and the patient’s name and
address), charts, and exams including
radiological reports. Id. at 377–78.
Respondent also testified that
‘‘sometimes [the patients] would * * *
also submit physical exams.’’ 5 Id. at 378.
Respondent maintained that he would
‘‘call the patients because [he] want[ed]
to actually talk to the patients before
[he] made any decisions on the patient,’’
that ‘‘[t]he history was very important,’’
id. at 378–79, and that the calls would
last an average of twenty minutes. Id. at
615. He also testified that he performed
a telephonic consultation with every
patient he prescribed to. Id. at 614–15.
Relatedly, Respondent maintained
that based on his experience as a pain
doctor, he could ‘‘get a sense of whether
the patient was telling me the truth
because certain pains in certain areas
elicit certain responses.’’ Id. at 379. He
also testified that most patients did not
‘‘have the savvy’’ to dupe him and that
‘‘sometimes [he] would lead patients
down the wrong path to see if they were
telling the truth * * * because there are
a lot of drug seekers out there.’’ Id. at
381–82. He also stated that if a patient
prescription he issued during a defined period of
time.
5 Respondent testified that ‘‘on the average,’’ the
physical exam had to be no more than
‘‘approximately six months’’ old, but that
‘‘sometimes we required records more recent than
six months and sometimes patient[s] could have
records up to eight months [old] or more.’’ Tr. 571.
Respondent maintained, however, that in each
instance, he would have a conversation with a
patient before prescribing and that this provided
‘‘an independent basis’’ to determine whether the
patient’s symptoms were continuing.’’ Id. at 572.
Moreover, the ‘‘Consent for Treatment’’ forms that
are in several patient files indicate that a patient
could receive the ‘‘first prescription with an
agreement that I will fax my medical records and
a photo ID * * * within 27 days and before my
next prescription is due for refill.’’ RX 11, at G0156
(signed on ‘‘12/8/04’’); RX 10, at G0151 (signed on
‘‘12/5/05’’). This suggests that in some instances,
Respondent may have issued prescriptions without
even reviewing a patient’s records.
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told him something that did not match
what was in their medical record, ‘‘we
would either call their primary doctor’’
or ‘‘deny them.’’ Id. at 382. Respondent
also testified that he ‘‘denied a lot of
patients and some of the records will
show that.’’ Id.
The ALJ found that some of
Respondent’s testimony was
contradicted in several material respects
by other evidence. See ALJ at 12 (¶ 36).
While Respondent testified that he
never prescribed without conducting a
telephone consultation with the patient,
and that the consultations lasted twenty
minutes on average, Ms. A.B., who
received hydrocodone pursuant to a
prescription issued by Respondent on
December 8, 2004, see GX 17, stated to
a DI that within a couple of hours after
she faxed medical records to Liberty,6
she received a telephone call from a
doctor which lasted approximately ‘‘one
minute.’’ GX 35, at 1–2. The doctor,
whose name she did not recall, asked
her what her pain was. Id. at 2. Ms. A.B.
told the doctor that she had previously
been treated by a doctor in North
Carolina for headaches caused by nerve
damage incurred in an automobile
accident; the doctor then agreed to
prescribe for her, ninety tablets of
hydrocodone/apap.7 Id. Ms. A.B. further
stated that the doctor did not discuss
with her how her progress would be
monitored, what to do if she
experienced side effects, and how to
contact him in an emergency. Id.
Another DI interviewed K.B., who had
also obtained a combination drug
containing hydrocodone through the
Liberty Web site. See GX 21; Tr. 116–
151. K.B. told the DI that she had
become aware of Liberty through a popup ad and that she went to the Web site
and filled out a questionnaire. Tr. 117.
On August 4, 2004, K.B. sent Liberty an
MRI report showing that she had a
herniated disk. Id. at 118; RX 15, at
G0190–91. ‘‘A couple of days later,’’ Tr.
118, K.B. was contacted by a woman
who stated that she was a representative
of Liberty. Id. According to K.B., the
woman performed a consultation and
told K.B. that a prescription had been
approved by Respondent.8 Id. at 118 &
131.
6 Those records included a progress note dated
September 16, 2004, which indicated that A.B.’s
physician had prescribed ninety Lorcet (10/650
mg.), with no refills. RX 6, at G0050. Lorcet is a
schedule III controlled substance which combines
hydrocodone with acetaminophen. See PDR, at
1287.
7 Apap is an abbreviation for acetaminophen.
8 Having found that K.B. faxed a copy of the MRI
report on August 4, 2004, four months before
Respondent began his contract with Liberty, I find
that Respondent did not issue the initial
prescription which K.B. received from Liberty. I do
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On or about December 15, 2004, K.B.
received ninety tablets of Lortab
(hydrocodone/apap (10/500)), a
schedule III controlled substance,
pursuant to a prescription issued by
Respondent. Id. at 119–20, GX 21; see
also PDR at 3240. K.B. received
approximately twenty-five prescriptions
through Liberty, the majority of which
were authorized by Respondent. Tr. 132,
141, 148, 150. K.B. never had a
conversation with Respondent, id. at
140, and had no contact with Liberty
with respect to any of the subsequent
orders she placed other than when she
contacted the Web site to determine the
status of an order. Id. at 121. K.B.
further told the DI that she became
addicted to hydrocodone. Id. at 122.
K.B. also obtained drugs from another
Web site during a portion of the period
in which she obtained drugs through
Liberty; her primary care physician did
not know that she was acquiring drugs
through the internet. Id. at 120–22.9
DEA Investigators also attempted to
contact the persons identified in
Respondent’s Exhibits 19–45, as
patients who were denied prescriptions.
Tr. 470. The DIs could not contact most
of the individuals and were able to
speak with only eight of them. See id.
at 634–44. Of these eight persons, the
record establishes that Respondent
prescribed to only one of them, Ms. S.A.
See GX 26.10 More specifically, on
find, however, that Respondent issued a
prescription to K.B. on December 15, 2004. See GX
21.
9 Investigators also attempted to interview several
other persons whose names were listed on the
prescription sheets found during the trash runs.
Some of the individuals could not be located, Tr.
162 & 165, others were uncooperative. Id. at 163.
Investigators were unable to contact the persons
named on the prescription labels because the labels
did not contain addresses. Id. at 169.
10 For example, while a DI spoke to L.L.’s
daughter (RX 20), she did not know whether her
mother ever spoke with Respondent. Tr. 635. R.T.
(RX 24) stated that he never received drugs from
Liberty, Tr. 637, and there is no evidence to the
contrary. While M.A. stated that he did not speak
with Respondent, id. at 637–38, documentary
evidence indicated that Respondent did not issue
a prescription because he felt that M.A. ‘‘IS
WANTING MEDS FOR SOMEONE ELSE.’’ RX 26.
Again, there is no evidence establishing that
Respondent issued a prescription to M.A.
A.F. (RX 27) acknowledged taking Vicodin and
sending medical records somewhere. Tr. 638. He
did not, however, remember where, id.; and in any
event, there is no evidence that Respondent
prescribed to him. M.K. (RX 31) acknowledged
receiving hydrocodone from Liberty ten times, that
he received his first order without a consultation,
and that his ‘‘subsequent orders usually did involve
a two to three minute conversation with someone
claiming to be a physician or a physician’s
assistant.’’ Tr. 640. Again, there is no evidence
establishing that Respondent (as opposed to other
doctors who worked for Liberty) prescribed to him.
RX 31.
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December 7, 2004, Respondent
prescribed to S.A. ninety tablets of
hydrocodone/apap (7.5/750 mg.).
Ms. S.A. stated that she ordered
hydrocodone from Liberty ‘‘at least ten
times and that she did not speak to any
physician on the first two occasions.’’ 11
Tr. 643. S.A. further stated that on
subsequent orders, she had ‘‘very short
conversations lasting approximately one
minute or less,’’ but could not recall the
name of any person she had talked to.
Id. at 643–44.
Respondent testified that S.A.’s
medical record supported the
prescription he issued and that the drug
and dosage he prescribed was
appropriate for her condition. Tr. 451.
Yet the evidence suggests that the most
recent medical report available to
Respondent was an ‘‘Operative Report’’
for a procedure which had been
performed nearly eight months earlier.
See RX 7, at G0112. Moreover,
Respondent offered no explanation as to
why S.A.’s condition was of such a
nature as to justify prescribing based on
an eight-month-old report.
A DI also interviewed R.Z., to whom
Respondent prescribed 90 tablets of
Vicodin ES (7.5/750 mg.), on January 5,
2005. GX 18. R.Z. told the DI that she
had become aware of Liberty in
approximately November 2004;
someone at Liberty put R.Z. in contact
with a man ‘‘who claimed to be a
doctor.’’ Tr. 72. R.Z. could not, however,
remember the name of the doctor, but
did recall having a phone conversation
of ‘‘approximately ten minutes’’
duration with him in which she was
asked questions about her condition,
what type of pain she had, what type of
pain medication she needed, how she
tolerated pain medications, and her
blood pressure. Id. at 73. The doctor
then told R.Z. that he would prescribe
to her ninety tablets of Vicodin. Id. at
74. R.Z. also told the DI that she had
faxed to Liberty an x-ray report which
showed that she had a bulging disk.12
M.B. (RX 33) acknowledged that he received
hydrocodone from Liberty four times and ‘‘recalled
talking to someone at the Liberty Meds Web site but
[did not] remember who.’’ Tr. 641. K.K. (RX 36)
acknowledged ordering hydrocodone ‘‘four or five’’
times, but identified a different doctor as the
prescriber. Tr. 641–42. Similarly, T.A. (RX 37)
stated that he had ordered hydrocodone from
Liberty ‘‘two or three’’ times, and that he had
conversations with either a doctor or physician’s
assistant lasting ‘‘two to three minutes,’’ but could
only identify a different doctor as the person he
spoke to. Id. at 642. As above, there is no evidence
establishing that Respondent prescribed to either
M.B. or T.A.
11 Here again, the evidence shows that S.A. faxed
her records to Liberty on August 25, 2004, four
months before Respondent began his contract with
Liberty. RX 7, at G0113–14.
12 R.Z. stated that she had sent in only the x-ray
report and filled out an online questionnaire. Tr. 89.
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Id. R.Z. further told the DI that she had
received from Liberty monthly
prescriptions for ninety tablets of
Vicodin over ‘‘a thirteen to fourteenmonth period.’’ 13 Id. at 77–78.
Respondent testified that the
prescription he issued was consistent
with the findings contained in the x-ray
report. Id. at 459; RX 10, at G0154. The
x-ray report contains the notations:
‘‘Record Received on 1/31/05,’’ and
‘‘Verified on 1/31/05 By MW.’’ Id. In
addition, the record includes a
handwritten note dated ‘‘1/31/05,’’
which states in relevant part: ‘‘Attention
Leisha, Here are the results of the xray
I had on my back. * * * I would like
my refill sent when it becomes time to
do so.’’ Id. at G0153. Respondent further
testified that ‘‘I don’t see a physical
exam here but it would be something
that we would require.’’ Tr. 459. He also
maintained that in order for R.Z. to get
an x-ray, ‘‘she had to have some
history,’’ because ‘‘you can’t refer
yourself for an x-ray.’’ Id.
Even so, that a patient needs a referral
to obtain an x-ray, does not establish
that Respondent reviewed R.Z.’s history
and a physical exam report before he
prescribed to her. Indeed, the absence of
a physical exam report in R.Z.’s file is
consistent with her statement that she
sent in only the x-ray report. See Tr. 89.
I therefore find that contrary to
Respondent’s testimony, he did not
review a physical exam report before
prescribing to R.Z.14
As for Respondent’s statement that
the Vicodin prescription he issued to
R.Z. was consistent with the findings of
the x-ray report, the evidence shows
that he issued the prescription on
January 5, 2005, nearly four weeks
R.Z. was never directed to obtain further tests (such
as a new x-ray), and stated that she did not believe
that Liberty ever contacted her primary doctor. Id.
at 79, 89–90.
13 R.Z. also stated that she had conversations
every three to four months regarding her condition
with a woman from Liberty who claimed to be a
physician. Tr. 76, 87. R.Z. testified that she had a
single conversation with a male caller. Id. at 96.
14 The ALJ noted that it ‘‘is unclear * * *
whether or not the Respondent had access to, or
actually reviewed medical records prior to
prescribing controlled substances to any of Liberty’s
customers discussed at the hearing.’’ ALJ at 19 n.10.
While this is correct with respect to some patients,
with respect to R.Z., it is clear that Respondent
prescribed without having any medical records that
supported the prescription.
In the context of discussing his prescribing
through Liberty, Respondent also testified that ‘‘I
will always’’ have some ‘‘data’’ and ‘‘I won’t just
place them on a prescription.’’ Tr. 442. Perhaps
Respondent was testifying about his prescribing
practices at the time of the hearing. Or perhaps he
considered the answers Liberty’s customers gave to
the questionnaires to be ‘‘data.’’ In any event, the
evidence establishes that he prescribed to R.Z.
without either reviewing a physical exam report or
the x-ray report.
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before Liberty received the x-ray report.
Respondent therefore could not have
issued the prescription on the basis of
the report.
With respect to K.B. (whose interview
with a DI is described above),
Respondent also maintained that a
report for an MRI which had been done
ten months earlier, see RX 15, at G0190;
established that the hydrocodone
prescription he issued was appropriate.
Tr. 467. Respondent then testified that
Respondent ‘‘had been on Toradol and
Ultram and had not received results.’’
Id. Continuing, Respondent stated that
‘‘[s]he also had gotten Lortab it seems.
If you look at G0195, in the middle
where it says 2/19/04, it says renewed
her Lortab and Flexeril.’’ Id. at 467–68.
Notably, both pages G0194 and
G0195, which appear to contain
progress notes of various visits K.B.
made to an orthopedic clinic between
January 15, 2003, and November 29,
2004, have the notations: ‘‘Record
Received on 1/31/05,’’ and ‘‘Verified on
1/31/05 By MW.’’ RX 15, at G0194–95.
Moreover, each page has a header
indicating that it was faxed on January
31, 2005. See id. As found above,
Respondent issued the prescription to
K.B. on December 15, 2004,
approximately six weeks before these
documents were faxed to Liberty. GX
21. Here again, Respondent could not
have relied on the documents when he
issued the prescription to K.B.,
notwithstanding his testimony that ‘‘we
would require’’ a physical exam. Tr.
459.15
15 As found above, Respondent never spoke with
K.B. Tr. 140. During the period she was obtaining
controlled substances from Liberty, K.B. was under
the care of another physician; K.B., however, never
told the latter physician that she was receiving
drugs from Liberty. Id. at 122, 142–43.
Respondent maintained that Liberty was ‘‘unable
to provide all the records’’ because of problems it
was having with its ‘‘IT person.’’ Tr. 410. However,
the files for some of the patients appear extensive,
see RXs 3 (22 pages), 5 (18 pages), 6 (64 pages), 7
(17 pages), & 14 (23 pages), thus prompting the
question of why Liberty was able to provide so
much documentation for these patients but not for
some of the others. Moreover, the patient files
indicate that the patients almost always faxed or
mailed their records to Liberty. Thus, even if the
records were scanned into Liberty’s computer
system, Respondent offered no evidence to establish
what happened to the original records. Finally,
there is no evidence that Respondent requested a
subpoena for the records. While the ALJ apparently
found that Respondent credibly testified that he did
not receive all of the information he requested, ALJ
Dec. at 13 n.3., I conclude that the patient files
Respondent introduced into evidence fairly reflect
the patient files as obtained by Liberty.
The ALJ further reasoned that Respondent’s
testimony supported ‘‘the requirement that [he]
maintain his own patient records.’’ Id. It is further
noted that under the New Jersey Board of Medical
Examiners’ regulation which governs the
prescribing of controlled substances, ‘‘[t]he
practitioner shall keep accurate and complete
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Other Patients
On January 5, 2005, Respondent
issued a prescription to K.A., a Texas
resident, for ninety tablets of
hydrocodone/apap (10/500mg). GX 27.
The record contains extensive progress
notes showing that K.A. was being
treated by a San Antonio, Texas pain
management specialist during 2004 and
2005 for neck pain.16 See RX 3.
Respondent testified that K.A. ‘‘has
various different problems * * * that
would cause one to have a ton of severe
pain.’’ Tr. 426. Respondent testified that
based on his review of the record, the
medication and dosage he prescribed
was appropriate. Id. at 432. Respondent
offered no testimony, however, as to
whether he contacted the pain
management specialist who was treating
K.A. See generally id. at 426–32.
On December 20, 2004, Respondent
prescribed to P.G., a Minnesota resident,
ninety tablets of hydrocodone/apap (10/
500 mg.) with one refill. GX 19.
Although the most recent progress note
in P.G.’s record, which was dated April
13, 2004, indicated that he had
‘‘[c]hronic low back with right lower
extremity radicular pain,’’ and that his
local physician had issued him a
prescription for twenty tablets of
Percocet p.r.n., P.G.’s physician further
observed that ‘‘[l]ong-term use of
narcotics for back pain is not in his best
interest and therefore he is given only
20 tablets at this time.’’ RX 4, at G0024.
While Respondent testified that his
prescription was appropriate, Tr. 435,
when asked on cross-examination
whether the eight-month-old progress
note was of sufficient recency to make
a diagnosis, he testified: ‘‘It really
depended also on the patients and the
physical findings but this does seem
like it was two months later than we
usually accept. * * *’’ Id. at 525.
On January 5, 2005, Respondent
prescribed to D.C., a resident of Georgia,
ninety tablets of hydrocodone/apap (10/
325 mg.). GX 24. The most recent
progress note in her file prior to this
prescribing was dated June 24, 2004,
and indicated that the physician’s
impression was: ‘‘Probable right C7
records.’’ N.J. Adm. Code 13:35–7.6(g) (emphasis
added). There is, however, no requirement under
federal law that an ‘‘individual practitioner * * *
keep records of controlled substances in Schedules
II, III, IV, and V which are prescribed in the lawful
course of professional practice, unless such
substances are prescribed in the course of
maintenance or detoxification treatment of an
individual.’’ 21 CFR 1304.03. I do not decide
whether it was permissible under the New Jersey
regulation for Respondent to maintain medical
records through the Liberty Web site.
16 Based on the progress notes as well as K.A.’s
Texas driver’s license, I find that K.A. was a
resident of Texas. See RX 3, at G0001.
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radiculopathy.’’ RX 5, at G0035. When
asked by his counsel whether this
would ‘‘indicate that pain should be in
a particular area?,’’ Respondent
answered: ‘‘Yes, she should have the
pain in the right upper extremity. If I
had spoken with this person about
giving her a treatment, I would have
first tried to elicit where her pain was
coming from.’’ Tr. 437 (emphasis
added). Respondent then discussed the
findings of a physical exam which
occurred on April 21, 2005, and which
he obviously could not have relied on
when he issued the prescription three
months earlier. See id. at 437–38.
Next, Respondent maintained that he
would try to confirm with the patient
whether their reported pain matched
with ‘‘what it should be.’’ Id. at 439. He
also maintained that his prescribing was
consistent with the drug (Vicodin 7.5)
that the physician, who physically
examined her three months later, had
prescribed. Id. at 440; RX 5, at G0032.
On cross-examination, Respondent
acknowledged that while the medical
records showed that D.C. had been by
an orthopedist and neurologist, neither
had referred her to him. Tr. 527. When
asked what his treatment plan was for
D.C., Respondent could not recall. Id.
He also did not refer her to a pain clinic
near where she lived. Id. at 528.
On December 15, 2004, Respondent
prescribed to S.K., a resident of Texas,
ninety tablets of hydrocodone/apap (10/
325mg.), with one refill. GX 22. Again,
Respondent testified that the
prescription he wrote ‘‘would be
consistent with what she’s experiencing
on physical exam here.’’ Tr. 454. While
Respondent testified that S.K.’s records
‘‘were accessed through PSDoctor,’’ id.
at 455; the only medical exam report in
S.K.’s file is dated ‘‘6/1/05,’’ and was
faxed on June 10, 2005. See RX 8, at
G0129–31. Respondent therefore could
not have relied on the report in issuing
the prescription.
On January 6, 2005, Respondent
prescribed to S.B., a South Carolina
resident, ninety tablets of Lortab (10/
500mg.). GX 27. SB’s patient file
contains only three documents: a copy
of her driver’s license, a ‘‘consent for
treatment’’ form dated ‘‘12/8/04,’’ and
the results of a blood test taken on
October 28, 2003. See RX 11.
Respondent maintained that S.B.’s file
was ‘‘incomplete,’’ and that ‘‘she
would’’ have been asked to provide
other data. Tr. 460. The ALJ did not,
however, make any findings regarding
the credibility of Respondent’s
testimony pertaining to S.B. In light of
the other instances in which
Respondent prescribed even though a
patient’s file was missing information, I
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10087
find that it is more likely than not that
he prescribed to S.B. without obtaining
any additional medical documentation.
On January 5, 2005, Respondent
prescribed to K.S., a resident of Texas,
ninety tablets of hydrocodone/apap (10/
500) with one refill. GX 29. K.S.’s
records include extensive progress notes
which show that she had last been seen
by a physician on September 28, 2004,
and had last been prescribed a
controlled substance (codeine/apap) on
December 20, 2004. RX 14, at G0182.
Respondent testified that ‘‘[i]t seemed
like she had really good follow-up here
according to these progress notes,’’ Tr.
462–63, and that the prescription he
wrote ‘‘would be appropriate for’’ the
condition documented in the record. Id.
at 465. Respondent offered no
explanation as to why he was
prescribing to a patient who had
received a controlled substance
prescription from another physician
only two weeks earlier. Moreover, given
his acknowledgment that K.S.’s records
showed that she was receiving good
follow-up care, he offered no testimony
that he had contacted K.S.’s physician
to coordinate her care and ensure that
she was not engaged in doctor
shopping.17
On January 3, 2005, Respondent
prescribed ninety tablets of
hydrocodone/apap (10/325 mg.) to E.M.,
a New Hampshire resident.18 Beside two
copies of E.M.’s driver’s license, her
patient file contains two forms: (1) A
Family and Medical Leave Act
certification that E.M. had a serious
illness, and (2) an Office of Workers
Compensation Programs’ form
documenting a medical examination
(performed on October 1, 2004) and
diagnosis and supporting the need for
certain restrictions on E.M.’s workrelated duties. See RX 16 at G0200–01.
The latter form indicates that E.M. had
low back pain and tendonitis in her
hand and shoulder. Id. at G0201. The
form, however, contains no
17 K.S.’s file includes a letter which forwarded
some records to Liberty. On the letter, there is a
handwritten notation that the records had been
reviewed, but that the clinic, which treated K.S.,
was ‘‘closed for lunch.’’ RX 14, at G0170.
18 While the ALJ found that E.M. was a Texas
resident, ALJ at 27 (FOF 90), RX 16 includes copies
of E.M.’s driver’s license which appears to indicate
that she was a New Hampshire resident. Moreover,
the fax header indicted that the documents were
faxed to Liberty from a phone number with a 603
area code, which is an area code for New
Hampshire.
The ALJ also noted that the prescription label (GX
29) was dated ‘‘1/3/04.’’ ALJ at 27 n.18. Based on
the undisputed evidence that Respondent did not
commence working for Liberty until December
2004, the ALJ found that the actual date of the
prescription was January 3, 2005. Id.; see also Tr.
535. I adopt this finding.
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documentation of her vital signs. See id.
Moreover, when asked by his counsel
whether the prescription he issued to
E.M. was appropriate, Respondent
answered that ‘‘we do prescribe
medicine for’’ tendonitis and carpal
tunnel, but that ‘‘it seems like this chart
is incomplete,’’ Tr. 469, and that ‘‘[i]t
might have been missing EMGs or other
things.’’ Id. at 536. He again testified
that it was his practice to look for other
data before prescribing such as
‘‘radiographic or EMGs.’’ Id. at 537.
While Respondent acknowledged that
E.M.’s record did not have any such
data, he then maintained that ‘‘this
might be an incomplete record.’’ Id.
Yet several of the documents
contained in E.M.’s patient file indicate
that they were faxed to Liberty on
December 31, 2004. Id. at G0202–03.19
Again, Respondent offered no credible
explanation as to why E.M’s file as
turned over to him had these documents
(which Liberty obtained shortly before
he issued the prescription to her) but
not the others which ‘‘might have been
missing.’’ Id. at 536. I therefore find that
there were no such additional
documents in E.M.’s patient file when
he prescribed to her.
On December 15, 2004, Respondent
issued to L.F., a resident of New Jersey,
a prescription for ninety tablets of
hydrocodone/apap (7.5/750mg.) with
one refill. GX 23. Respondent testified
that L.F.’s records showed that his
physician ‘‘did a physical exam,’’ and
that ‘‘[t]here is also one on 10/8/04 by
the same physician which was
consistent with what was found on 10/
8/03, * * * you can see the same
vertebral bodies marked off, so it’s very
consistent with what the patient is
having.’’ Tr. 456. Respondent
maintained that L.F. had a condition
which ‘‘merit[ed] intervention for pain,’’
id., and that the dosage he prescribed
was consistent with his condition. Id. at
457.
On cross-examination, the
Government asked Respondent to
compare the handwriting of the two
reports of ‘‘Examination Findings,’’
which were dated ‘‘10/8/03’’ and ‘‘10/8/
04’’ respectively. Id. at 530; see also RX
9, at G0142 & G0145. Respondent
acknowledged that ‘‘[a]ll the
handwriting [on the two reports] is in
exactly the same position.’’ Tr. 530.
19 Again, while Respondent testified that the
records that he requested from Liberty were
incomplete, he offered no explanation as to why
Liberty was able to provide some records for a
patient but not the missing ones. Moreover, the
evidence indicates that many of the patients faxed
their records to Liberty. Even if these records were
scanned into a database, Respondent offered no
evidence as to what became of the original
documents.
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Respondent testified, however, that
when he prescribed to L.F., he ‘‘did not’’
recognize that one of the documents had
probably been falsified. Id. Moreover,
none of the documents in L.F’s file
contained his vital signs. See RX 9. And
as with the other Liberty patients,
Respondent did not physically examine
L.F., even though he lived in northern
New Jersey, and near where he
practiced.20 See id. at G0147, GX 23.
On December 7, 2004, Respondent
prescribed to L.W., another New Jersey
resident, ninety tablets of hydrocodone/
apap (10/325 mg.) with one refill. GX
20. L.W.’s patient file consisted of three
pages: a progress note dated June 17,
2004, a sheet indicating that L.W. was
faxing her driver’s license, and a blurred
copy of a driver’s license. See RX 12.
The progress note lists several
diagnostic codes and under the
handwritten notation of ‘‘CODES,’’
states: ‘‘polycystic ovaries,’’
‘‘adhesions,’’ and ‘‘pelvic pain.’’ RX 12,
at G0158. Next to the column for
history, the document includes a
notation of ‘‘Percocet # 120.’’ Id.
With respect to L.W., Respondent
maintained that ‘‘[t]hese patients have
pelvic pain generally to the lower
abdomen.’’ Tr. 461. Respondent then
testified that ‘‘[t]here is no radiological
exam that you would do to tell you
anything differently[,] [b]ut obviously
they know she has polycystic ovaries
according to this physician’s history and
physical.’’ Id. Respondent testified that
the prescription was appropriate for a
patient with this condition, and that he
believed someone had verified L.W.’s
identity with her physician because
‘‘her license was blurred.’’ Id.
Respondent did not, however, testify
that he called Respondent’s physician.
Respondent’s Other Evidence
Respondent also testified that he had
proposed that Liberty use a narcotic
20 Respondent practiced pain management at a
clinic in Livingston, New Jersey. RX 1; ALJ at 5. L.F.
lived in Wallington, and L.W. lived in Warren, New
Jersey. RXs 20 & 23. In accordance with 5 U.S.C.
§ 556(e), I take official notice of the fact that all
three of these cities are located in northern New
Jersey. See 5 Rand McNally, Business Traveler’s
Road Atlas 62, 68–69 (1994). Notwithstanding the
proximity of his clinic to L.F.’s and L.W.’s
residences, Respondent did not require them to
appear for a physical examination.
An agency ‘‘may take official notice of facts at any
stage in a proceeding—even in the final decision.’’
U.S. Dept. of Justice, Attorney General’s Manual on
the Administrative Procedure Act 80 (1947). In
accordance with the Administrative Procedure Act
and DEA’s regulation, Respondent is ‘‘entitled on
timely request to an opportunity to show to the
contrary.’’ 5 U.S.C. 556(e); see also 21 CFR
1316.59(e). Accordingly, Respondent may file a
motion for reconsideration within fifteen days of
service of this order which shall commence with
the mailing of the order.
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contract under which a patient was
required to agree not to give or sell his
drugs to others, as well as not to seek
drugs from other physicians. Tr. 384;
see also RX 11, at G0156. According to
the contract, a patient would be
dismissed for failing to comply. Tr. 384.
Yet Respondent was not ‘‘sure how’’
Liberty determined whether a patient
was obtaining drugs from other sources
such as another Web site. Id. at 385.
Respondent gave conflicting
testimony as to whether he had
prescribed oxycodone to Liberty’s
patients. First, he testified that he did so
at a frequency that was ‘‘pretty much
equal’’ to that of his hydrocodone
prescribing. Id. at 585. Later, however,
when Respondent was asked by the ALJ
as to whether he ever recalled
prescribing schedule II controlled
substances to a Liberty patient, he
appeared to backtrack from this
testimony answering: ‘‘Yes, there was a
patient in our system you mean.’’ Id. at
605.21
Respondent further testified that he
believed that his prescribing practices
complied with New Jersey’s regulations
and were consistent with a 2001 DEA
Guidance Document. With respect to the
New Jersey regulation, which provides
that ‘‘a practitioner shall not dispense
drugs or issue prescriptions to an
individual, * * * without first having
conducted an examination, which shall
be appropriately documented in the
patient record,’’ except for in six
defined circumstances, N.J. Admin Code
§ 13:35–7.1A, Respondent testified that
exceptions three (‘‘[f]or continuation
medications on a short term basis for a
new patient prior to the patient’s first
appointment’’) and four (‘‘[f]or an
established patient who, based on sound
medical practice, the physician believes
does not require a new examination
before issuing a new prescription’’),
‘‘could apply.’’ Tr. 589; see also N.J.
Admin. Code § 13:35–7.1A(b)(3) & (4).
Respondent did not, however, identify
any patient he prescribed to over the
21 The ALJ also found that Respondent authorized
refills of schedule II controlled substances and that
he ‘‘was unaware of the forms needed to actually
prescribe a schedule II controlled substance.’’ ALJ
14 (citing Tr. 604–05). Respondent testified,
however, that he was not ‘‘aware of’’ ‘‘a requirement
for a Schedule II substance to be prescribed on a
specifically identified form.’’ Tr. 605.
Except for in an emergency situation, the
dispensing of a schedule II controlled substance
requires ‘‘a written prescription signed by the
practitioner,’’ and the ‘‘original written, signed
prescription [must be] presented to the pharmacist
for review prior to the actual dispensing of the
controlled substance.’’ 21 CFR 1306.11(a). However,
no special form is required to prescribe a schedule
II drug and Respondent’s testimony was correct.
Federal law does, however, prohibit the refilling of
a schedule II controlled substance. 21 U.S.C. 829(a).
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Internet who later came in for an
appointment. Nor did he testify that any
of the persons whose names were found
on the prescription sheets and labels
was an established patient.
Respondent also maintained that his
Internet prescribing was consistent with
the statements in this Agency’s
Guidance Document, Dispensing and
Purchasing Controlled Substances Over
the Internet, 66 FR 21181 (2001). More
specifically, Respondent maintained
that his practices were consistent with
the Guidance Document because ‘‘[w]e
always had the patient’s chief
complaint, history was taken, a physical
examination was done by another
physician, and we collected all the
evidence together and then I made my
decision based on all the evidence
including the radiographical evidence.’’
Tr. 417. Respondent further maintained
that ‘‘it was not’’ his practice to
prescribe based solely on Internet
correspondence. Id.
Finally, Respondent’s counsel read to
him the following question and answer
from the Guidance Document:
I am a Physician. Does the need for a
Physical Exam Mean that I Cannot Engage in
Telemedicine and Prescribe Controlled
Substances?
No, DEA does not intend to limit the
ability of doctors to engage in telemedicine.
If the patient cannot travel to your office, but
you supervise an exam given by a nurse or
other professional, you can then prescribe the
needed medications based on the results, to
the extent that State law allows. In this case,
your decision on the appropriateness of the
medication is based on facts (symptoms,
blood pressure, etc.) that have been verified
by a qualified third party and observed by
you electronically.
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GX 6, at 5; Tr. 418.22
Respondent was then asked by his
counsel whether his Internet practice
was consistent with this statement. Tr.
418–19. Respondent answered: ‘‘Yes. In
fact, we’ve exceeded those, also
communicating with the physicians, not
just electronically but via telephone.’’
Id. at 419. Respondent then explained
that ‘‘the radiographical reports were
read by a physician radiologist, the
physical exams were done by another
physician, so sometimes we have a
couple of physicians involved in the
process. Id.23
Respondent did not, however,
identify a single instance in which he
supervised and observed a physical
22 At the hearing, Respondent’s counsel slightly
altered the text of the answer published in the
Guidance Document. The alteration did not,
however, materially change the meaning of the
answer.
23 Respondent also testified that the first time he
saw the 2001 Guidance Document was at the
hearing. Tr. 522.
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exam as it was being performed by
another qualified medical professional.
Moreover, Respondent did not have any
recollection as to having spoken to any
of the physicians who were identified in
the patient records that were introduced
into evidence in this proceeding. Id. at
573. Finally, he was unaware as to
whether any of the patient notes he
made were ever sent by Liberty to the
primary care physicians of those he
prescribed to. Id. at 614. He also never
gave written referrals for Liberty
patients to see local doctors. Id. at 512.
Respondent testified that he had
stopped performing telemedicine
consultations for Liberty in late
December of 2005. Id. at 487. He also
represented that it was not his ‘‘present
intention’’ to resume internet based
prescribing. Id.
As noted above, Respondent
introduced into evidence a number of
printouts from Liberty’s software with
the heading ‘‘Patient Information for
Appointment.’’ See RXs 19–45. These
printouts establish that in several
instances, patients were denied drugs
because they were receiving them from
other sources. See RXs 19, 21, 27, 32,
33, 39. Moreover, in other instances
Respondent did not approve a
prescription, see RX 23, 34, 43; and in
at least one case, Respondent denied a
prescription because he felt the person
‘‘was wanting meds for someone else.’’
RX 26. Moreover, the printouts suggest
that in other instances, either Liberty or
Respondent denied requests because the
person was seeking the drugs too soon,
RX 22, 35, 36; the patient’s records had
not been verified, RX 28; or the patient
needed to be evaluated and send in
records before Respondent approved a
refill. RX 42 & 44. Only one of these
printouts, however, corresponds with a
patient (S.A.) who was identified above
as having received a prescription which
was issued by Respondent.24 Compare
RX 44 with GX 26.
24 The National Center on Addiction and
Substance Abuse (CASA) has reported that ‘‘[t]he
number of people who admit abusing controlled
prescription drugs increased from 7.8 million in
1992 to 15.1 million in 2003.’’ National Center on
Addiction and Substance Abuse, Under the
Counter: The Diversion and Abuse of Controlled
Prescription Drugs in the U.S. 3 (2005) (GX 3).
Moreover, ‘‘[a]pproximately six percent of the U.S.
population (15.1 million people) admitted abusing
controlled prescription drugs in 2003, 23 percent
more than the combined number abusing cocaine
(5.9 million), hallucinogens (4.0 million), inhalants
(2.1 million) and heroin (328,000).’’ Id. Relatedly,
‘‘[b]etween 1992 and 2003, there has been a * * *
140.5 percent increase in the self-reported abuse of
prescription opioids’’; in the same period, the
‘‘abuse of controlled prescription drugs has been
growing at a rate twice that of marijuana abuse, five
times greater than cocaine abuse and 60 times
greater than heroin abuse.’’ Id. at 4.
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Discussion
Section 304(a) of the Controlled
Substances Act (CSA) provides that a
registration to ‘‘dispense a controlled
substance * * * may be suspended or
revoked by the Attorney General upon
a finding that the registrant * * * has
committed such acts as would render
his registration under section 823 of this
title inconsistent with the public
interest as determined under such
section.’’ 21 U.S.C. 824(a)(4). With
respect to a practitioner, the Act
requires the consideration of the
following factors in making the public
interest determination:
(1) The recommendation of the appropriate
State licensing board or professional
disciplinary authority.
(2) The applicant’s experience in
dispensing * * * controlled substances.
(3) The applicant’s conviction record under
Federal or State laws relating to the
manufacture, distribution, or dispensing of
controlled substances.
(4) Compliance with applicable State,
Federal, or local laws relating to controlled
substances.
(5) Such other conduct which may threaten
the public health and safety.
Id. section 823(f).
‘‘[T]hese factors are * * * considered
in the disjunctive.’’ Robert A. Leslie,
M.D., 68 FR 15227, 15230 (2003). I ‘‘may
rely on any one or a combination of
factors, and may give each factor the
weight [I] deem[] appropriate in
determining whether a registration
should be revoked.’’ Id. Moreover, I am
‘‘not required to make findings as to all
of the factors.’’ Hoxie v. DEA, 419 F.3d
477, 482 (6th Cir. 2005); see also Morall
v. DEA, 412 F.3d 165, 173–74 (D.C. Cir.
2005).
In this matter, it is undisputed that
neither the State of New York nor the
CASA has further reported that teenagers
‘‘represent an especially vulnerable group,’’ because
‘‘[t]eens may view prescription drugs as relatively
safe either when abused alone or in combination
with alcohol or other drugs.’’ Id. According to
CASA, ‘‘[i]n 2003, 2.3 million teens ages 12 to 17
(9.3 percent) reported abusing a controlled
prescription drug in the past year; 83 percent of
them reported abusing opioids.’’ Id. Moreover,
‘‘[b]etween 1992 and 2002, the number of [first
time] teenage prescription opioid abusers increased
by 542 percent.’’ Id. at 35.
Finally, CASA noted that ‘‘[i]nternet sites not
adhering to state licensing requirements, medical
board standards or federal law have enabled
consumers to obtain controlled prescription drugs
without a valid prescription or physician
supervision and without regard to age.’’ Id. at 63.
CASA also noted that ‘‘illegal [i]nternet pharmacies
have introduced a new avenue through which
unscrupulous buyers and users can purchase
controlled substances for unlawful purposes.’’ Id.
Moreover, ‘‘[t]he age of the customers appears not
to be an issue for Internet pharmacies,’’ and that
there are ‘‘no mechanisms in place to block
children from purchasing controlled drugs over the
Internet.’’ Id. at 66.
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State of New Jersey has taken action
against Respondent’s medical license
(factor one). It is also undisputed that
Respondent has not been convicted of
an offense related to controlled
substances under federal or state law
(factor three).25 This proceeding
focused, however, on Respondent’s
experience in dispensing controlled
substances and his record of compliance
with applicable laws. As discussed
below, the evidence pertaining to these
factors is disturbing and establishes—at
a minimum—that Respondent
committed numerous violations of both
Federal and state laws.
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Factor Two and Four—Respondent’s
Experience in Dispensing Controlled
Substances and Record of Compliance
With Applicable Controlled Substance
Laws
Under a longstanding DEA regulation,
a prescription for a controlled substance
is not ‘‘effective’’ unless it is ‘‘issued for
a legitimate medical purpose by an
individual practitioner acting in the
usual course of his professional
practice.’’ 21 CFR 1306.04(a). This
regulation further provides that ‘‘an
order purporting to be a prescription
issued not in the usual course of
professional treatment * * * is not a
prescription within the meaning and
intent of [21 U.S.C. 829] and * * * the
person issuing it, shall be subject to the
penalties provided for violations of the
provisions of law relating to controlled
substances.’’ Id. As the Supreme Court
recently explained, ‘‘the prescription
requirement * * * ensures patients use
controlled substances under the
supervision of a doctor so as to prevent
addiction and recreational abuse. As a
corollary, [it] also bars doctors from
peddling to patients who crave the
drugs for those prohibited uses.’’
Gonzales v. Oregon, 546 U.S. 243, 274
(2006) (citing United States v. Moore,
423 U.S. 122, 135 (1975)).
Under the CSA, it is fundamental that
a practitioner must establish a bonafide
doctor-patient relationship in order to
act ‘‘in the usual course of * * *
professional practice’’ and to issue a
prescription for a ‘‘legitimate medical
purpose.’’ Moore, 423 U.S. at 141–43.
The CSA, however, generally looks to
state law to determine whether a doctor
and patient have established a bonafide
doctor-patient relationship. See Kamir
Garces-Mejias, 72 FR 54931, 54935
(2007); United Prescription Services,
Inc., 72 FR 50397, 50407 (2007);
25 Under settled precedent, neither of these
factors is dispositive. See Edmund Chein, 72 FR
6580, 6590 n.22 (2007); Mortimer B. Levin, 55 FR
8209, 8210 (1990).
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Dispensing and Purchasing Controlled
Substances Over the Internet, 66 FR at
21182–83.26
Moreover, ‘‘[a] physician who engages
in the unauthorized practice of
medicine’’ under state laws ‘‘is not a
‘practitioner acting in the usual course
of * * * professional practice’’’ under
the CSA. United Prescription Services,
72 FR at 50407 (quoting 21 CFR
1306.04(a)). As explained therein, this
rule is supported by the plain meaning
of the Act, which defines the ‘‘[t]he term
‘practitioner’ [to] mean[] a physician
* * * licensed, registered, or otherwise
permitted, by the United States or the
jurisdiction in which he practices * * *
to * * * dispense * * * a controlled
substance,’’ 21 U.S.C. 802(21), and
‘‘[t]he term ‘dispense’ [to] mean[] to
deliver a controlled substance to an
ultimate user * * * by, or pursuant to
the lawful order of, a practitioner.’’ Id.
section 802(10). See also id. section
823(f) (‘‘The Attorney General shall
register practitioners * * * to dispense
* * * if the applicant is authorized to
dispense * * * controlled substances
under the laws of the State in which he
practices.’’).
As I noted in United Prescription
Services, shortly after the CSA’s
enactment, the Supreme Court
explained that ‘‘[i]n the case of a
physician [the Act] contemplates that he
is authorized by the State to practice
medicine and to dispense drugs in
connection with his professional
practice.’’ Moore, 423 U.S. at 140–41
(emphasis added) (quoted at 72 FR
50407). A controlled-substance
prescription issued by a physician who
lacks the license or other authority
required to practice medicine within a
State is therefore unlawful under the
CSA. See 21 CFR 1306.04(a) (‘‘An order
purporting to be a prescription issued
not in the usual course of professional
treatment * * * is not a prescription
within the meaning an intent of’’ the
CSA); cf. 21 CFR 1306.03(a)(1) (‘‘A
prescription for a controlled substance
26 On October 15, 2008, the President signed into
law, the Ryan Haight Online Pharmacy Consumer
Protection Act of 2008, Pub. L. 110–425, 122 Stat.
4820 (2008). Section 2 of the Act prohibits the
dispensing of a prescription controlled substance
‘‘by means of the Internet without a valid
prescription,’’ and defines, in relevant part, the
‘‘[t]he term ‘valid prescription’ [to] mean[] a
prescription that is issued for a legitimate medical
purpose in the usual course of professional practice
by * * * a practitioner who has conducted at least
1 in-person medical evaluation of the patient.’’ 122
Stat. 4820. Section 2 further defines ‘‘[t]he term ‘inperson medical evaluation’ [to] mean[] a medical
evaluation that is conducted with the patient in the
physical presence of the practitioner, without
regard to whether portions of the evaluation are
conducted by other health professionals.’’ Id. These
provisions do not, however, apply to Respondent’s
conduct.
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may be issued only by an individual
practitioner who is * * * [a]uthorized
to prescribe controlled substances by
the jurisdiction in which he is licensed
to practice his profession[.]’’).27
Under the regulation of the New
Jersey Board of Medical Examiners, ‘‘a
practitioner shall not dispense drugs or
issue prescriptions to an individual
* * * without first having conducted an
examination, which shall be
appropriately documented in the patient
record.’’ N.J. Admin Code § 13:35–
7.1A(a). This rule further requires that
‘‘[a]s part of the patient examination, the
practitioner shall’’:
1. Perform an appropriate history and
physical examination;
2. Make a diagnosis based upon the
examination and all diagnostic and
laboratory tests consistent with good medical
care;
3. Formulate a therapeutic plan and
discuss such plan, along with the basis for
the plan and the risks and benefits of various
treatment options, with the patient; and
4. Ensure the availability of the physician
or coverage for appropriate follow-up care.
Id.
It is undisputed that Respondent did
not perform a physical examination on
any of the Liberty patients he prescribed
to, including those who were New
Jersey residents. Instead, Respondent
asserted that two exceptions provided in
the New Jersey rule ‘‘could apply’’ to his
internet prescribing. Tr. 589. The first of
these authorizes the prescribing of
‘‘continuation medications on a short
term basis for a new patient prior to the
patient’s first appointment’’; the second
authorizes prescribing ‘‘[f]or an
established patient who, based on sound
medical practice, the physician believes
does not require a new examination
before issuing a new prescription.’’ N.J.
Admin Code 13:35–7.1A(b)(3) & (4).
As the record establishes, none of
Respondent’s Liberty patients were ever
expected to see him for a ‘‘first
appointment,’’ and none did. Moreover,
Respondent offered no evidence that
any of his Liberty patients were his
‘‘established patients.’’ 28
27 As the California Court of Appeal has noted:
the ‘‘proscription of the unlicensed practice of
medicine is neither an obscure nor an unusual state
prohibition of which ignorance can reasonably be
claimed, and certainly not by persons * * * who
are licensed health care providers. Nor can such
persons reasonably claim ignorance of the fact that
authorization of a prescription pharmaceutical
constitutes the practice of medicine.’’ Hageseth v.
Superior Court, 59 Cal. Rptr.3d 385, 403 (Ct. App.
2007).
28 I acknowledge that in Gonzales, the Supreme
Court stated that ‘‘[a]s for the federal law factor,
though it does require the Attorney General to
decide ‘[c]ompliance’ with the law, it does not
suggest he may decide what the law says. Were it
otherwise, the Attorney General could
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In his brief, Respondent also contends
that New Jersey’s exception ‘‘[f]or a
patient examined by a healthcare
professional who is in collaborative
practice with the practitioner’’ also
applies. Id. § 13:35–7.1A(b)(5); see Resp.
Prop. Findings 52. However, with
respect to this exception, Respondent
testified that ‘‘I don’t know what
collaborative means there,’’ Tr. 589, and
in any event, there is no credible
evidence that Respondent collaborated
with any of the practitioners who may
have previously examined the Liberty
patients. Id. at 573 & 614.
Respondent thus failed to establish a
legitimate doctor-patient relationship
under the New Jersey regulation. I
therefore further hold that Respondent’s
prescriptions to the Liberty patients
were not ‘‘issued for a legitimate
medical purpose by an individual
practitioner acting in the usual course of
his professional practice,’’ 21 CFR
1306.04(a) and thus violated the CSA as
well.
Respondent’s prescriptions also
violated numerous laws of the States
where the patients were located.
Respondent prescribed controlled
substances to two residents of Georgia,
A.B. and D.C. Under the rules of the
Georgia Composite State Board of
Medical Examiners, it is
‘‘unprofessional conduct’’ to
‘‘[p]rovid[e] treatment and/or
consultation recommendations via
electronic or other means unless the
licensee has performed a history and
physical examination of the patient
adequate to establish differential
diagnoses and identify underlying
conditions and/or contra-indications to
the treatment recommended.’’ Ga.
Comp. R. & Regs. 360–3.02(6).29
authoritatively interpret ‘State’ and ‘local laws,’
which are also included in 21 U.S.C. 823(f), despite
the obvious constitutional problems in his doing
so.’’ 546 U.S. at 264.
In determining whether Respondent established a
legitimate doctor-patient relationship with the
Liberty patients, this Agency must necessarily
examine state law. Moreover, the requirement that
a practitioner must generally perform a physical
exam in order to properly diagnose a patient is one
which is universally accepted throughout the
medical community and by state medical boards.
See American Medical Association, Guidance for
Physicians on Internet Prescribing (GX 8); see also
Federation of State Medical Boards, Internet
Prescribing Language By State (available at https://
www.fsmb.org/ncip_resources.html/).
Notably, Respondent cites no decision of either
the New Jersey Board of Medical Examiners or the
New Jersey courts holding that conduct similar to
his internet prescribing was lawful under the
exceptions which he contended ‘‘could apply.’’ Tr.
589. If Respondent had, this Agency would, of
course, respect that decision.
29 It is noted that the rule does ‘‘not prohibit a
licensee who is on call or covering for another
licensee from treating and/or consulting a patient of
such other licensee.’’ Ga. Comp. R. & Regs. 360–3–
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Moreover, Respondent violated Georgia
law because he engaged in the
unlicensed practice of medicine. See Ga.
Code Ann. § 43–34–31.1.30
Respondent also prescribed controlled
substances to four residents of Texas,
S.A., K.A., S.K., and K.S. Respondent
did not hold a Texas medical license.
See Tex. Occup. Code § 155.001; see
also id. § 151.056(a) (‘‘A person who is
physically located in another
jurisdiction but who, through the use of
any medium, including an electronic
medium, performs an act that is part of
a patient care service initiated in this
state, * * * and that would affect the
diagnosis or treatment of the patient, is
considered to be engaged in the practice
of medicine in this state and is subject
to appropriate regulations by the
board.’’); 22 Tex. Admin. Code
§ 174.4(c) (‘‘Physicians who treat and
prescribe through the Internet are
practicing medicine and must possess
appropriate licensure in all jurisdictions
where patients reside.’’).
Respondent also lacked the state
registration required to prescribe a
controlled substance. See Tex. Health &
Safety Code § 481.061(a) (requiring state
registration to dispense); id.
§ 481.063(d) (requiring as a condition
for registration that ‘‘a practitioner [be]
licensed under the laws of this state’’).
Respondent thus also violated Texas
law, and the CSA, in prescribing
controlled substances to that State’s
residents. See Moore, 423 U.S. at 140–
41 (‘‘In the case of a physician [the CSA]
contemplates that he is authorized by
the State to practice medicine and to
dispense drugs in connection with his
professional practice.’’) (emphasis
added); United Prescription Services, 72
FR at 50407 (‘‘A controlled-substance
prescription issued by a physician who
lacks the license [or other authority
required] to practice medicine within a
State is * * * unlawful under the
.02(6). Respondent did not maintain that he was
covering for, or consulting with, other physicians
who were treating either A.B. or D.C.
30 This statute provides:
(a) A person who is physically located in another
state * * * and who, through the use of any means,
including electronic * * * or other means of
telecommunication, through which medical
information or data is transmitted, performs an act
that is part of a patient care service located in this
state * * * that would affect the diagnosis or
treatment of the patient is engaged in the practice
of medicine in this state. Any person who performs
such acts through such means shall be required to
have a license to practice medicine in this state and
shall be subject to regulation by the board.
Ga. Code Ann. § 43–34–31.1(a). While the statute
includes exceptions when, inter alia, the physician
‘‘[p]rovides consultation services at the request of
a physician licensed in this state,’’ or ‘‘[p]rovides
consultation services in the case of an emergency,’’
id. § 43–34–31.1(b)(1) & (2), neither exception
applies to Respondent.
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CSA.’’); 21 U.S.C. 802(10) (defining
‘‘ ‘dispense’ [to] mean[] to deliver a
controlled substance to an ultimate user
* * * by, or pursuant to the lawful
order of, a practitioner’’).
Respondent prescribed a controlled
substance to R.Z., a Massachusetts
resident. Massachusetts law follows
nearly verbatim the CSA’s prescription
requirement. Compare Mass. Gen. Laws
ch. 94C, § 19(a), with 21 CFR 1306.04(a).
In December 2003, the Massachusetts
Board of Registration in Medicine
issued the following interpretation of
the State’s prescription law:
[t]o satisfy the requirement that a
prescription be issued by a practitioner in the
usual course of his professional practice,
there must be a physician-patient
relationship that is for the purpose of
maintaining the patient’s well-being and the
physician must conform to certain minimum
norms and standards for the care of patients,
such as taking an adequate medical history
and conducting an appropriate physical and/
or mental status examination and recording
the results. Issuance of a prescription, by any
means, including the Internet or other
electronic process, that does not meet these
requirements is therefore unlawful.
Commonwealth of Massachusetts, Board
of Registration in Medicine, Policy 03–
06 INTERNET PRESCRIBING (Adopted
Dec. 17, 2003).31 As the Board’s
interpretation makes plain, Respondent
acted outside of the usual course of
professional practice when he
prescribed a controlled substance to
R.Z., and therefore violated both
Massachusetts law and the CSA.32
31 The ALJ also noted that Respondent was
required to be licensed to practice medicine in
Massachusetts and that ‘‘[o]nly a practitioner who
is authorized to prescribe controlled substances
may do so.’’ ALJ at 39 (citing Mass. Gen. Laws. ch.
94C, § 18(a)). In light of the Massachusetts’ Board
clear interpretation as set forth in its policy on
Internet Prescribing, I conclude that it is
unnecessary to address whether Respondent also
violated the State’s provisions requiring a license
and controlled substance registration which appear
to allow an out-of-state practitioner to issue a
prescription to a state resident in some instances.
Id. § 18(c).
32 The ALJ also found that Respondent violated
Minnesota law when he prescribed to P.G. because
he lacked either a state medical license or a
telemedicine registration. ALJ at 39–40 (citing
Minn. Stat. § 147.081). The ALJ observed that
Minnesota allows a physician to provide
telemedicine services if four conditions are met
including that the physician register with the State.
ALJ at 40 (citing Minn. Stat. § 147.032 Subd. 1(a)).
The Minnesota statute, however, exempts a
physician who holds a valid license to practice in
another state ‘‘if * * * the services are provided on
an irregular or infrequent basis,’’ which is defined
as ‘‘if the person provides the services less than
once a month or provides the services to fewer than
ten patients annually.’’ Id. Subd. 2(2).
The Government’s evidence established that
Respondent issued only a single prescription to
P.G.; there is no evidence that he prescribed to any
other Minnesota residents. While it may well be the
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Respondent also issued a prescription
for controlled substance to E.M., a New
Hampshire resident. In April 2004, the
New Hampshire Board of Medicine
issued Guidelines on internet
prescribing. In pertinent part, the Board
stated:
The members of the NH Board of Medicine
have interpreted that a sufficient examination
in the establishment of a valid physicianpatient relationship cannot take place
without an initial face-to-face encounter with
the patient. It requires at a minimum: (1)
Verifying the person requesting the
medication is who they claim to be; (2)
establishing a diagnosis through the use of
acceptable medical practices, such as patient
history, mental status exam, physical exam,
and appropriate diagnostic and laboratory
testing by the prescribing physician; (3)
discussing with the patient the diagnosis and
the evidence for it, and the risks and benefits
of various treatment options; and (4) ensuring
availability of the physician or coverage for
the patient for appropriate follow-up care;
(which usually includes a face-to-face
encounter at least once a year and as often
as is necessary to assure safe continuation of
medication). Complete management of a
patient by Internet, e-mail, or other forms of
electronic communication is inappropriate.
Id. Continuing, the regulation states that
forming ‘‘a proper relationship’’ requires
that a physician:
(1) Personally perform an appropriate
history and physical examination, make a
diagnosis, and formulate a therapeutic plan.
This process must be documented
appropriately; and
(2) Discuss with the patient the diagnosis
and evidence for it, and the risks and benefits
of various treatment options; and
(3) Insure the availability of the physician
or coverage for appropriate follow-up care.
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New Hampshire Board of Medicine,
Guidelines for Physician Internet and
Telephone Prescribing (April 7, 2004).
Moreover, under New Hampshire law,
‘‘[a]ny person shall be regarded as
practicing medicine * * * who shall
diagnose, treat * * * or prescribe any
treatment of medicine for any disease or
human ailment.’’ N.H. Rev. Stat. § 329:1.
Moreover, practicing medicine without
a license or as ‘‘otherwise authorized
according to the law of’’ the State
constitutes the ‘‘unlawful practice’’ of
medicine.33 Id. § 329:24. I thus conclude
that Respondent acted outside of the
usual course of professional practice in
prescribing a controlled substance to
E.M. and violated both New Hampshire
law and the CSA.
Respondent also prescribed a
controlled substance to S.B., a South
Carolina resident. In May 2001, the
South Carolina Board of Medical
Examiners promulgated its regulation
on ‘‘Contact with Patients before
Prescribing.’’ S.C. Code Regs. 81–28.
This regulation declares that ‘‘[i]t is
unprofessional conduct for a physician
to initially prescribe drugs to an
individual without first establishing a
proper physician-patient relationship.’’
Id.34 Here too, Respondent failed to
establish a valid doctor-patient
relationship with S.B. under South
Carolina law and thus violated the CSA
when he prescribed a controlled
substance to her. 21 CFR 1306.04(a).
Respondent also issued a prescription
to K.B., a resident of Alabama. Under
Alabama law, ‘‘[t]he practice of
medicine * * * across state lines means
the practice of medicine * * * as
defined in Section 34–24–50(1), as it
applies to * * * [t]he rendering of
treatment to a patient located within
this state by a physician located outside
this state as a result of transmission of
individual patient data by electronic or
other means from this state to such
physician or his or her agent.’’ Ala.
Code § 34–24–501(a); see also id. § 34–
24–50 (defining the ‘‘practice of
medicine’’ as meaning ‘‘[t]o diagnose,
treat, correct, advise or prescribe for any
human disease, ailment, injury,
infirmity, deformity, pain or other
condition, physical or mental, real or
imaginary, by any means or
instrumentality’’). Moreover, under
Alabama law, ‘‘[n]o person shall engage
in the practice of medicine * * * across
state lines in this state * * * unless he
* * * has been issued a special purpose
license to practice medicine * * *
across state lines.’’ Id. § 34–24–502(a).
Respondent did not hold either a
medical license or a special purpose
license to practice medicine across state
lines as required by Alabama law. In
issuing the prescription to K.B.,
Respondent not only violated Alabama
law, he acted outside of the usual course
of professional practice and thereby
violated the CSA as well.
As the foregoing demonstrates,
Respondent repeatedly violated both the
CSA and various State laws in
prescribing to Liberty’s customers.
Respondent nonetheless contends that
case that Respondent issued additional
prescriptions to P.G. or other Minnesota residents,
the Government has not proved that he engaged in
the unauthorized practice of medicine within
Minnesota.
33 Respondent produced no evidence that his
internet practice came within any of the exceptions
to New Hampshire’s licensing requirement. See
N.H. Rev. Stat. § 329:21.
34 Similar to other State’s regulations (such as
New Jersey’s), the South Carolina rules recognizes
several circumstances in which a physician can
lawfully prescribe to a patient he had not
personally examined. See S.C. Code of Regs. R. 81–
28(B). Respondent has not, however, demonstrated
that his prescribing to S.B. came within any of the
exceptions that excuse a physician from personally
examining his patient before prescribing.
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the Supreme Court’s decision in
Gonzales ‘‘indicates that the
continuation of his registration should
not turn on [this Agency’s]
determination of whether in fact he had
satisfied the relevant standards for
establishing a doctor-patient
relationship.’’ Resp. Br. at 51; see also
id. at 52 (arguing that Gonzales
‘‘militates against a determination by
the agency, for purposes of determining
whether [Respondent’s] registration
should be revoked, as to whether [his]
practices with internet patients satisfied
state * * * standards for effective
medical practice’’).
Contrary to Respondent’s view,
Gonzales expressly recognized that one
of the core purposes of the prescription
requirement was to ‘‘ensure[] [that]
patients use controlled substances
under the supervision of a doctor so as
to prevent addiction and recreational
abuse.’’ 546 U.S. at 274. Respondent’s
internet prescribing practices beg the
question of how he was supervising the
persons to whom he prescribed, to
prevent them from becoming addicted
to, or engaging in recreational abuse of,
the drugs.35 Examining whether
Respondent established legitimate
doctor-patient relationships under state
law with those to whom he prescribed,
is thus a necessary incident of
determining whether he violated the
CSA.
Respondent further argues that the
DEA 2001 Guidance ‘‘does not require
the doctor personally to take the history
or perform the [physical] examination.’’
Resp. Br. at 50. Relatedly, Respondent
contends that ‘‘in terms of the indicia’’
of a legitimate doctor-patient
relationship as stated in the Guidance,
‘‘there is clearly room for a physician to
issue a prescription premised in part
upon an examination or history
conducted by another professional.’’ Id.
At the hearing, however, Respondent
testified that he had not seen the
Guidance prior to this proceeding, Tr.
35 Respondent contends that his internet practice
‘‘was not substantially different from the evaluation
process he would perform when he was contacted
by a nurse from [the hospital] while he was on
call,’’ in that ‘‘without examining the patient
directly, [he] would draw upon his substantial
experience and expertise to get the information he
needed * * * to determine what care the patient
required.’’ Response to Gov.’s Exceptions at 5. It
does not require a degree in medicine, however, to
recognize that there is a critical difference between
the two situations. In the on-call situation, a nurse
is personally observing the patient and likely
relating the patient’s vital signs and other
information regarding the patient’s symptoms/
condition to the physician. In contrast, even when
Respondent, in the course of his internet
prescribing, reviewed the results of physical
examinations, he had no current information
available as to the patient’s vital signs and other
symptoms.
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414–15; Respondent therefore could not
have been induced into believing that
his conduct was legal by the Guidance.
Moreover, the Guidance made clear that
its discussion of the criteria for
establishing a legitimate doctor-patient
relationship was based on a summary of
the standards adopted by the various
States. See 66 FR at 21182 (GX 6, at 4).36
As Respondent acknowledged, he did
not conduct his own review of state
laws or seek legal advice concerning the
legality of prescribing through the
Liberty website. At the time he
commenced his contract with Liberty,
numerous state medical boards had
already issued either policy statements
or regulations (including those States
discussed above) which addressed the
legality of a physician’s prescribing to
patients he had not personally
examined. Moreover, at the time
Respondent commenced his contract
with Liberty, this Agency had published
several final orders revoking
practitioners’ registrations based on
their prescribing over the internet and
without performing a physical
examination.37 See, e.g., Marvin L. Gibbs,
Jr., M.D., 69 FR 11658, 11661 (issued
Mar. 11, 2004); Mark Wade, M.D., 69 FR
7018, 7021–22 (issued Feb. 12, 2004);
Rick Joe Nelson, M.D., 66 FR 30752,
30753 (2001) (noting immediate
suspension of practitioner’s registration
based on internet prescribing).
In his response to the Government’s
Exceptions, Respondent contends that
because of Boswell’s ‘‘attentiveness to
regulatory and compliance issues,’’ he
was ‘‘led * * * to believe that his
internet practice would be proper.’’
Response to Gov.’s Exceptions 7. This is
not a persuasive argument. Indeed, one
would think that a licensed professional
and the holder of an appointment as a
clinical professor would be well aware
of such state laws and regulations as
those prohibiting the unauthorized
practice medicine and those defining
something as fundamental to the
practice of medicine as the steps
necessary to establish a legitimate
doctor-patient relationship. As the
36 The Guidance is not a regulation and thus does
not have the force and effect of law. Rather, it is
a Notice which simply provides guidance.
37 Respondent also contends that his shortfalls
were of one ‘‘seeking to practice in an area where
the technical requirements are both widely
dispersed and in flux.’’ Resp. Br. 46; see also id. at
52. However, at the time he commenced his
contract with Liberty, each of the States discussed
above had already either enacted laws, or issued
regulations or policy statements, addressing the
propriety of this activity. And in any event,
Respondent cannot credibly argue that his conduct
should be excused because the legal requirements
were in flux when he made no inquiry as to what
the requirements were.
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California Court of Appeal has
explained:
[the] proscription of the unlicensed practice
of medicine is neither an obscure nor an
unusual state prohibition of which ignorance
can reasonably be claimed, and certainly not
by persons * * * who are licensed health
care providers. Nor can such persons
reasonably claim ignorance of the fact that
authorization of a prescription
pharmaceutical constitutes the practice of
medicine.
Hageseth v. Superior Court, 59 Cal.
Rptr.3d 385, 403 (Ct. App. 2007).
Respondent further contends that his
case is distinguishable from other
Agency cases involving internet
prescribers. See Resp. Br. at 43–46.
More specifically, Respondent contends
that in contrast to other internet
prescribers, he ‘‘issued no more than a
handful of prescriptions a day,’’ that he
prescribed ‘‘only after reviewing the
patient’s medical record and conducting
a searching personal interview,’’ that he
‘‘only prescribed medications that were
pertinent to his area of medical
expertise,’’ and that he ‘‘rejected many
requests for medication that he deemed
inappropriate.’’ Id. at 43. Relatedly,
Respondent contends that Liberty
attempted to identify persons who were
obtaining drugs from multiple sources
and that it verified medical records. Id.
at 45. He also contends that ‘‘[h]e
genuinely made a good faith effort’’ to
practice ‘‘medicine properly and
effectively.’’ Resp. to Gov.’s Exceptions
at 10.
As to these contentions, the evidence
is mixed. While there is no evidence
rebutting his contention that he issued
only a small number of prescriptions
each day, by his own admission he
consulted for Liberty for approximately
one year during which he issued
between 800 and 1200 prescriptions.
However, the record does not establish
the extent to which these prescriptions
were for controlled substances.
Moreover, he continued to prescribe for
three months after being served with the
Order to Show Cause.38 While it seems
38 With respect to his prescribing following the
service of the Show Cause Order, Respondent does
not maintain that he did not prescribe controlled
substances in this period. Rather, he argues that I
should consider the fact that the Order alleged that
he ‘‘improperly prescribed drugs [phentermine and
phendimetrazine] that he never in fact prescribed.’’
Response to Gov.’s Exceptions at 11. Respondent
ignores, however, that the Show Cause Order also
quoted the prescription requirement of 21 CFR
1306.04(a), and the New Jersey regulation setting
forth the requirements for prescribing a drug
including that a ‘‘practitioner shall * * * perform
an appropriate history and physical examination.’’
Show Cause Order at 1 & 3. Moreover, the Show
Cause Order alleged that Respondent was
prescribing to persons that he was not physically
examining and had no prior doctor-patient
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10093
likely that he prescribed controlled
substances during this period, the
Government did not establish the scope
of his controlled substance prescribing
activity after he was served with the
Order.
Moreover, notwithstanding his
contention that he prescribed only after
reviewing a patient’s medical record
and ‘‘conducting a searching’’ interview,
the evidence establishes that in some
instances (R.Z. and S.K.) he prescribed
before Liberty even obtained the
records, and that in other instances he
relied on records that—according to his
own testimony—were outdated (P.G)
and even indicated that narcotics were
not in the patient’s best interest.
Relatedly, as the ALJ noted, other
evidence casts serious doubt as to his
assertions that he always conducted a
consultation with the patients, let alone
a searching interview of them. ALJ at 12.
(FoF 36).
On the other hand, there is some
evidence that Liberty rejected patients
who were seeking drugs from multiple
sources, or who were seeking drugs to
give to others. There is also evidence
that in some instances, Liberty verified
a patient’s records with the patient’s
original physicians although it is
unclear what this process involved and
how often it was undertaken.39
Relatedly, even though the patient files
typically included photocopies of a
driver’s license, there is no guarantee
that the drugs were actually going to
these persons.
Moreover, the ALJ found that
Respondent ‘‘declined to prescribe
medications in many instances where
Liberty customers were directed to
him.’’ ALJ at 17 (FoF 52). The
Government produced no evidence to
rebut Respondent’s contention as to the
frequency of his refusals to prescribe.
Relatedly, there is also evidence that
Respondent rejected a request for drugs
when he thought the person would
divert or was seeking drugs from
multiple sources. Moreover, there is
evidence that Respondent refused to
prescribe because a person’s complaint
(and the supporting records) had not
been verified.
relationship with, and was thus violating 21 CFR
1306.04. Id. at 6. The Show Cause Order thus
provided Respondent with fair warning as to the
illegality of his conduct.
39 For example, did Liberty’s employees simply
ask whether a person had been a patient? Did they
ask whether the patient was still being treated by
the physician? Did they ask what the physician’s
diagnosis was? And did they ask if there was any
evidence that the patient had engaged in drug
seeking behavior? Moreover, in some instances,
Respondent prescribed before the records were even
sent to Liberty. Finally, in at least one case (patient
L.F.), it appeared that some of the records were
fraudulent.
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While the record as a whole may not
conclusively show that Respondent
knowingly diverted, at the very least it
establishes that Respondent acted with
reckless disregard for his obligations as
a practitioner under both the CSA and
numerous state laws. Moreover,
Respondent acknowledged that he
prescribed schedule II drugs and
authorized refills of these prescriptions,
in violation of federal law. See 21 U.S.C.
829(a).40 The Government has therefore
proved that Respondent has committed
acts that render his registration
‘‘inconsistent with the public interest.’’
Id. § 824(a)(4).
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Sanction
Under Agency precedent, where, as
here, ‘‘the Government has proved that
a registrant has committed acts
inconsistent with the public interest, a
registrant must ‘‘ ‘present sufficient
mitigating evidence to assure the
Administrator that [he] can be entrusted
with the responsibility carried by such
a registration.’ ’’ Medicine ShoppeJonesborough, 73 FR 364, 387 (2008)
(quoting Samuel S. Jackson, 72 FR
23848, 23853 (2007) (quoting Leo R.
Miller, 53 FR 21931, 21932 (1988)).
‘‘Moreover, because ‘past performance is
the best predictor of future
performance,’ ALRA Labs, Inc. v. DEA,
54 F.3d 450, 452 (7th Cir. 1995), [DEA]
has repeatedly held that where a
registrant has committed acts
inconsistent with the public interest, the
registrant must accept responsibility for
[his] actions and demonstrate that [he]
will not engage in future misconduct.’’
Medicine Shoppe, 73 FR at 387; see also
Jackson, 72 FR at 23853; John H.
Kennedy, 71 FR 35705, 35709 (2006);
Prince George Daniels, 60 FR 62884,
62887 (1995). See also Hoxie v. DEA,
419 F.3d at 483 (‘‘admitting fault’’ is
‘‘properly consider[ed]’’ by DEA to be
an ‘‘important factor[]’’ in the public
interest determination).
The ALJ acknowledged that the
Government had ‘‘clearly
demonstrated’’ that Respondent’s
internet prescribing practices violated
the CSA. ALJ at 43. While the ALJ
recognized that Respondent’s internet
prescribing was ‘‘egregious conduct,’’
id., that he ‘‘fail[ed] to be totally truthful
40 Respondent also provided Liberty with an
electronic copy of his signature. Tr. 511 & 570.
While Respondent credibly testified that he had no
reason to suspect that Liberty was using his
signature to authorize prescriptions which he had
not approved, he acknowledged that he had no way
of determining whether Liberty was misusing his
signature. Id. at 570. This Agency has previously
held that failing to safeguard one’s signature
constitutes conduct inconsistent with the public
interest. See Robert G. Hallermeier, M.D., 62 FR
26818, 26820 (1997).
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during his testimony,’’ id. at 44, and that
he ‘‘demonstrated a lack of sound
judgment’’ in continuing his internet
prescribing for three months following
the service of the Show Cause Order, id.,
she also noted that he ‘‘is clearly a very
educated, dedicated and talented
physician,’’ id.; that he had been
practicing medicine for eleven years,
and that ‘‘the only instances of [his]
improper handling of controlled
substances were related to his’’ internet
prescribing. Id. Balancing Respondent’s
misconduct against his overall practice,
the ALJ recommended that I continue
his registration, subject only to the
condition that he not prescribe over the
internet. Id.
As explained above, this Agency has
repeatedly held that accepting
responsibility for one’s misconduct is an
‘‘important factor’’ in the public interest
determination. See Hoxie, 419 F.3d at
483 (upholding Agency’s consideration
of whether registrant/applicant has
admitted fault); Jackson, 72 FR at 23853;
Kennedy, 71 FR at 35709; Daniels, 60 FR
at 62887. The ALJ, however, made no
finding as to whether Respondent had
accepted responsibility for his
misconduct.
While Respondent testified that it was
not his ‘‘present intention’’ to resume
internet prescribing,41 the record as a
whole does not establish that he has
accepted responsibility for his
misconduct. I acknowledge that the DI
who served Respondent with the Show
Cause Order described him as
cooperative, and that Respondent
admitted that his internet prescribing
was even more extensive than that
shown by the Government. In his
testimony, however, Respondent
continued to maintain that his
prescribing without performing a
physical exam was lawful under New
Jersey’s regulation. Moreover,
Respondent did not acknowledge that
he violated either the CSA, or any other
state laws and regulations, whether they
related to the standards for establishing
a legitimate doctor-patient relationship
or addressed the unauthorized practice
of medicine. Respondent’s failure to
acknowledge the illegality of his
conduct does not inspire confidence
41 Notably, while the ALJ credited this testimony,
she was less than impressed with Respondent’s
testimony that he did not intend to resume internet
prescribing. See ALJ 15 n.4 (‘‘Although
[Respondent] appeared to be credible when he
testified here to his intent, I do question how he
resolves this intent with his continued interest in
telemedicine.’’). Indeed, intentions can change, and
Respondent’s statement is hardly an unequivocal
statement that he will not resume such conduct in
the future.
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that he will refrain from engaging in
similar acts in the future.
Moreover, while a registrant must
accept responsibility and demonstrate
that he will not engage in future
misconduct in order to establish that
his/her continued registration is
consistent with the public interest, these
are not the only factors that are relevant
in determining the appropriate sanction.
As I have previously noted, ‘‘[n]either
Jackson nor any other agency decision
holds * * * that the Agency cannot
consider the deterrent value of a
sanction in deciding whether a
registration should be [suspended or]
revoked.’’ Southwood Pharmaceuticals,
Inc., 72 FR 36487, 36504 (2007).42
In Southwood, I explained that ‘‘even
when a proceeding serves a remedial
purpose, an administrative agency can
properly consider the need to deter
others from engaging in similar acts.’’
Id. (citing Butz v. Glover Livestock
Commission Co., Inc., 411 U.S. 182,
187–88 (1973)). I further noted that the
‘‘[c]onsideration of the deterrent effect
of a potential sanction is supported by
the CSA’s purpose of protecting the
public interest, see 21 U.S.C. 801, and
the broad grant of authority conveyed in
the statutory text, which authorizes the
[suspension or] revocation of a
registration when a registrant ‘has
committed such acts as would render
[his] registration * * * inconsistent
with the public interest,’ id. section
824(a)(4), and [which] specifically
directs the Attorney General to consider
[‘such other conduct which may
threaten public health and safety,’ id.
section 823(f)].’’ Southwood, 72 FR at
36504.
I acknowledge that Respondent has
impressive credentials, and that except
for his internet prescribing, there is no
evidence that he violated the CSA or
state laws in his years of practice as an
anesthesiologist and pain management
specialist. However, under any
circumstance, Respondent’s conduct as
an internet prescriber would be
disturbing. That he holds an
appointment as a clinical professor
renders his conduct even more so.
Relatedly, Respondent’s testimony as to
why he believed that his Internet
prescribing was lawful and failed to
perform his own inquiries into the
legality of this practice is especially
unpersuasive and does not excuse his
failure to obey the law.
Moreover, Respondent’s Internet
prescribing was not a brief sojourn into
illegality. Rather, he engaged in his
42 Southwood was decided before the ALJ issued
her recommended decision in this matter. The ALJ
did not, however, even acknowledge the decision.
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misconduct for a year, during which
time he likely issued between 800 to
1,200 prescriptions. Yet the record does
not establish the extent to which these
prescriptions were for controlled
substances.43
I acknowledge that proceedings under
Section 304 are non-punitive. But even
were I to ignore that Respondent has not
accepted responsibility for his
misconduct, and credit his testimony
that he did not intend to resume his
internet practice, I would still conclude
that a lengthy suspension of his
registration is warranted.
As found above, the diversion and
abuse of prescription drugs has
increased dramatically, with the number
of people admitting to such abuse
(approximately 15.1 million) exceeding
by twenty-three percent, the number
who abuse cocaine, hallucinogens,
inhalants and heroin combined.
Moreover, the growth rate of
prescription drug abuse is twice the
growth rate of marijuana abuse and five
times the growth rate of cocaine abuse;
between 1992 and 2002, the growth in
prescription opioid abuse among
teenagers grew by 542 percent.
The use of the internet and telephone
to prescribe to individuals with whom
a physician has not established a bona
fide doctor-patient relationship is one of
the primary means by which controlled
substances are being diverted and
obtained for recreational abuse. The
growth of this means of diversion
represents a grave threat to public
health and safety. Accordingly, this
Agency has repeatedly revoked the
registrations of numerous practitioners
who have committed similar acts by
prescribing over the internet without
establishing legitimate doctor-patient
relationships. See, e.g., Kamir GarcesMejias, 72 FR 54931 (2007); William
Lockridge, 71 FR 77791 (2006); Mario
Diaz, 71 FR 70788 (2006). The ALJ did
not, however, even acknowledge any of
the numerous Agency decisions to this
effect.
Respondent maintains that his case is
distinguishable from these and other
reported decisions involving internet
43 It is also noted that Respondent continued his
internet prescribing for three months after he
received the Show Cause Order, even though the
Order put him on notice as to the requirements for
a lawful prescription under both the CSA and state
law. While Respondent did not dispute that he
prescribed controlled substances during this period,
I do not rely on this conduct in setting the sanction
because the Government did not identify a single
controlled substance prescription that he issued
following the service of the Show Cause Order. If
the Government had shown specific instances of
Respondent’s prescribing of controlled substances
following service of the Order, I would have found
that he knowingly diverted controlled substances
and revoked his registration.
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prescribers because he ‘‘genuinely
believed * * * that he was practicing
medicine properly and effectively[,]’’
and ‘‘genuinely made a good faith effort
to do so.’’ Response to Gov.’s Exceptions
at 10. He also contends that he ‘‘is an
extraordinarily dedicated and tireless
physician who saw the internet as a way
to care for more patients,’’ and that
while he ‘‘can be faulted’’ for ‘‘having
trusted colleagues and new business
associates when he should have been
more skeptical,’’ ‘‘the price should not
be his career.’’ Id. at 14.
It is true that in other Agency
decisions revoking the registrations of
internet prescribers, the evidence
strongly supported the conclusion that
the physicians were engaged in
intentional acts of diversion. Here, by
contrast, the evidence does not establish
that he knowingly distributed controlled
substances to those who were seeking
the drugs to abuse them or to sell them
to abusers. His conduct—which is
extraordinary for its recklessness—
nonetheless violated the CSA.
Continuing Respondent’s registration,
subject only to the condition that he
refrain from prescribing over the
Internet, is no sanction at all given the
numerous state laws and new Federal
law which prohibit this practice in the
manner Respondent engaged in it.
Adopting the ALJ’s recommendation
would not only ‘‘ignore how
irresponsibly [Respondent] acted,’’
Southwood, 71 FR at 36503; it would
also signal to others that one can ignore
the law (and his obligation to determine
what the law is) and yet incur no
consequence for having done so. Given
the extraordinary harm to public health
and safety caused by internet
prescribing, this is not the message that
should be sent to those who
contemplate prescribing controlled
substances in this manner. Rather, such
persons should understand that they are
responsible for knowing the law and
acting in conformity therewith, and that
there will be serious consequences for
those who fail to do so.
Accordingly, I conclude that
Respondent’s registration should be
suspended for a period of one year.
Moreover, Respondent’s pending
application for renewal of his
registration will be held in abeyance
during the course of the suspension.
Upon completion of the suspension, his
application will be approved provided
that he fulfills the following condition.
Because Respondent has not
acknowledged that his internet
prescribing practices violated the CSA,
he must provide a sworn statement to
this effect. If Respondent complies with
this condition (and he commits no other
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10095
acts which would warrant the denial of
his application), the Agency will
expeditiously grant his renewal
application. If, however, if he fails to do
so, his application will be denied.
Order
Pursuant to the authority vested in me
by 21 U.S.C. 823(f) & 824(a), as well as
28 CFR 0.100(b) & 0.104, I hereby order
that the DEA Certificate of Registration
issued to Joseph Gaudio, M.D., be, and
it hereby is, suspended for a period of
one year. I further order that
Respondent’s pending application to
renew his registration be, and it hereby
will be, held in abeyance pending the
completion of the period of suspension
and Respondent’s providing to this
Agency a sworn statement
acknowledging that his internet
prescribing activities violated the
Controlled Substances Act and DEA
regulations. This Order is effective April
8, 2009.44
Dated: February 26, 2009.
Michele M. Leonhart,
Deputy Administrator.
[FR Doc. E9–4903 Filed 3–6–09; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
Foreign Claims Settlement
Commission
F.C.S.C. Meeting Notice No. 2–09
The Foreign Claims Settlement
Commission, pursuant to its regulations
(45 CFR Part 504) and the Government
in the Sunshine Act (5 U.S.C. 552b),
hereby gives notice in regard to the
scheduling of meetings for the
transaction of Commission business and
other matters specified, as follows:
Date and Time: Wednesday, March
18, 2009, at 10:30 a.m.
Subject Matter: Issuance of Proposed
Decisions, Amended Proposed
Decisions, Final Decisions and Orders
in claims against Albania.
Status: Open.
All meetings are held at the Foreign
Claims Settlement Commission, 600 E
Street, NW., Washington, DC. Requests
for information, or advance notices of
intention to observe an open meeting,
may be directed to: Administrative
Officer, Foreign Claims Settlement
Commission, 600 E Street, NW., Room
44 Respondent can choose to commence serving
his suspension earlier by tendering his Certificate
of Registration and any order forms he has been
issued to the nearest DEA office.
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Agencies
[Federal Register Volume 74, Number 44 (Monday, March 9, 2009)]
[Notices]
[Pages 10083-10095]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-4903]
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. 06-28]
Joseph Gaudio, M.D.; Suspension of Registration
On September 16, 2005, the Deputy Assistant Administrator, Office
of Diversion Control, Drug Enforcement Administration, issued an Order
to Show Cause to Joseph Gaudio, M.D. (Respondent) of Alpine, New
Jersey. The Show Cause Order sought the revocation of Respondent's DEA
Certificate of Registration, which authorizes him to handle controlled
substances as a practitioner, and the denial of any pending
applications to renew or modify his registration, on the ground that he
had committed acts which rendered his continued registration
``inconsistent with the public interest.'' Show Cause Order at 1
(citing 21 U.S.C. 823(f) & 824(a)(4)).
The Show Cause Order alleged that Respondent had issued
prescriptions for controlled substances which lacked a legitimate
medical purpose, and that in doing so, he had acted outside of the
usual course of professional practice. Id. at 1 & 6. The Show Cause
Order specifically alleged that Respondent had ``prescrib[ed]
controlled substances to Internet customers despite never establishing
a genuine doctor-patient relationship with the Internet customer.'' Id.
at 5. Relatedly, the Show Cause Order alleged that Respondent ``did not
see customers, had no prior doctor-patient relationships with the
Internet customers, did not conduct physical exams, * * * did [not]
create or maintain patient records,'' and that ``[t]he only information
usually reviewed prior to issuing drug orders was the customer's online
questionnaire.'' Id. at 6.
The Show Cause Order also alleged that ``[a] review of
prescriptions filled by [Carrington Healthcare System/Infiniti Services
Group] revealed that [Respondent] ha[d] issued drug orders for
controlled substances to Internet customers throughout the United
States, including Georgia, Texas, Pennsylvania, Alabama, Louisiana, and
Kentucky.'' Id. The Show Cause Order further alleged that ``[a] review
of prescriptions filled by [Carrington/Infiniti] for the period October
13, 2004 to January 21, 2005, revealed that [Respondent] ha[d] issued
16 drug orders to Internet customers in at least nine different
states.'' Id.
On October 21, 2005, Respondent, through his counsel, requested a
hearing on the allegations. The matter was assigned to Administrative
Law Judge (ALJ) Gail Randall, who conducted a hearing on May 2-5, 2006,
in New York, NY. At the hearing, both parties put on testimony and
introduced documentary evidence. Thereafter, both parties submitted
briefs containing their proposed findings of fact, conclusions of law,
and arguments.
On November 2, 2007, the ALJ issued her recommended decision. In
her decision, the ALJ concluded that ``[t]he Government has clearly
demonstrated that the Respondent's Internet practice and his resulting
issuance of controlled substance prescriptions * * * violated the
Controlled Substances Act.'' ALJ at 43. Applying the totality of the
circumstances test, the ALJ concluded, however, that the revocation of
Respondent's registration was not warranted. Id. at 43-44.
The ALJ specifically noted that ``Respondent's conduct encompassed
a one year period,'' that Respondent had ``voluntarily cease[d]'' his
conduct, but that he had not done so until three months after he was
served with the Show Cause Order. Id. at 43. While the ALJ deemed
Respondent's cessation of his conduct as ``commendable because of its
voluntary nature,'' she further explained that he ``demonstrated a lack
of sound judgment'' in ``continuing to'' prescribe after being served
with the Show Cause Order. Id. at 44. The ALJ also found of concern
``Respondent's failure to be totally truthful during his testimony.''
Id.
The ALJ reasoned, however, that Respondent was ``a very educated,
dedicated and talented physician practicing in a sometimes difficult
specialty, pain management,'' and that the revocation of his
registration would render him ``being unable to handle controlled
substances'' in his specialty. Id. Because the record demonstrated that
Respondent had practiced medicine for eleven years, and that ``the only
instances of [his] improper handling of controlled substances were
related to his'' Internet prescribing, the ALJ recommended that
Respondent's registration be continued subject to the condition that he
``not engage in any activity involving prescribing controlled
substances and the Internet.'' Id.
Having considered the entire record in this matter, I hereby issued
this Decision and Final Order. I adopt the ALJ's conclusions that
Respondent violated both the Controlled Substances Act (CSA) and
various state standards of medical practice in issuing prescriptions to
persons who ordered drugs through an Internet site. For reasons
explained below, I reject the ALJ's recommended sanction as
inconsistent with agency precedent and will order the suspension of
Respondent's registration for a period of one year. I make the
following findings.
Findings
Respondent is a medical doctor who is board certified in both
anesthesiology and pain management and is licensed to practice medicine
in the States of New York and New Jersey. Tr. 488. Respondent is also
the holder of a DEA Certificate of Registration, which authorizes him
to dispense controlled substances in schedules II through V as a
practitioner. GX 1, at 2. While the expiration date of Respondent's
registration was September 30, 2006, Respondent submitted a renewal
application on August 4, 2006. See Reply to Respondent's Status Report,
at 1. I therefore find that Respondent's prior registration has
remained in effect pending the issuance of this Final Order and that
Respondent also has an application pending before the Agency. See 5
U.S.C. 558(c).
Respondent attended medical school at The Autonomous University of
Guadalajara, and the New York Medical College. RX 1, at 2.
Subsequently, Respondent did his residency in anesthesiology at St.
Luke's/Roosevelt Hospital, an institution which is affiliated with the
Columbia University College of Physicians and Surgeons, where he
received an award given to the Outstanding Graduate Resident in
Anesthesiology. Id. Respondent also did a fellowship in Pain Management
at the Memorial Sloan Kettering Cancer Center, where he was elected
Chief Fellow. Id. at 1.
Upon completion of his fellowship, Respondent joined New Jersey
Anesthesia Associates (NJAA), a group of physicians which provides
anesthesia services at St. Barnabas Medical Center. Tr. 345-47.
Respondent is a partner in NJAA. Id. at 347. In addition to providing
anesthesia, Respondent also treats both acute and chronic pain
patients. Id. at 555-56. Respondent is also an attending physician and
clinical professor at St. Barnabas, where he trains residents in
anesthesia. Id. at 360.
Respondent came to the attention of the Agency during its
investigation of a
[[Page 10084]]
large criminal conspiracy which was run by Johar Saran, and which used
the Internet to unlawfully distribute controlled substances. Id. at
156-159; see also GX 16 (Indictment, United States v. Saran, et al.,
No. 305-CR-0240P (N.D. Tex. 2005). As part of the investigation, DEA
Investigators conducted trash runs at the premises of Carrington Health
Care System, an entity owned by Saran which was located at 301 E.
Stephens, Suite 100, Arlington, Texas. Tr. 159, 185. During the trash
runs, investigators found various documents including ``Drug
Prescription'' sheets and copies of some prescription labels which are
placed on pill vials. See GXs 17-29.
The ``Drug Prescription'' sheets listed a patient's name, address,
birth date, age, sex, phone number, medication history, and allergies.
See GXs 17-24. In the block titled ``Physician,'' the sheets listed
Respondent's name, address, phone numbers, and DEA number. Id. In the
block titled ``Rx,'' the sheets gave the date, drug name (which in each
instance was a schedule III controlled substance containing
hydrocodone), quantity, number of refills, instructions for taking the
drug, instructions to the pharmacist as to whether substitution was
permitted or the drug was to be dispensed as written, and bore the
electronic signature of Respondent. See id. In a block entitled
``Pharmacy Services Use Only,'' each of the sheets listed a number, as
well as the date and time of a consultation, and included the notation
``LBRTY.'' Id. \1\ Finally, each of the sheets included shipping
information. Id.
---------------------------------------------------------------------------
\1\ At the top of all but one of the sheets was the notation:
``From: Dr. Joseph Gaudio, M.D.,'' and a date and time which was
typically only a short period after the date and time listed for the
consultation. See GXs 17, 18, 20, 21, 22, 23.
---------------------------------------------------------------------------
The prescription labels listed ``Triphasic Pharmacy,'' with an
address of ``301 E. Stephens St. Ste 100'' in Arlington as the
dispensing pharmacy. GXs 25-31. The labels also listed the patient's
name, the drug, a date, the quantity dispensed, a prescription number,
instructions for taking the drug, number of refills, and a physician's
name. Id. Respondent was listed as the prescribing physician on eight
of the prescription labels, each of which indicated that the customer
had received a schedule III controlled substance containing
hydrocodone. See id.
Several months later, Respondent was served with the Show Cause
Order. Tr. 51-52. When asked by a DI whether he had prescribed over the
Internet, Respondent admitted that ``he had a contract with a company
called Liberty Med,'' that ``he reviewed on-line patient applications
of Liberty Med,'' and that he ``was paid $20 per on-line patient
consultation.'' Id. at 52. Respondent also told the DI that he reviewed
MRIs and X-rays. When asked if he maintained patient records,
Respondent told the DI that Liberty Med ``kept them.'' Id. at 53.
In his testimony, Respondent explained that in October 2004, one of
his partners in NJAA introduced him to Liberty Medical and Mr. Craig
Boswell, whose mother ran the company. Tr. 371-72. Respondent's partner
told him that ``he understood [that Liberty] was a legitimate company
that practices Internet-based medicine and that I might be interested
in talking to Craig Boswell concerning possibly doing work for them.''
Id. at 371.
Respondent met with Boswell, who told him that the company ``was
not one of these companies opening and shutting in a week or month,
[that it] was a legitimate company, [and that] they wanted to set up
consultation services doing this internet website.'' Id. at 373.
Boswell further advised Respondent that Liberty ``deal[t] with patients
who have medical records, who have been seen by other physicians, who
have radiological evidence of pain.'' Id. Boswell also told Respondent
that Liberty would carefully screen the patients, that ``they would
make sure that the patient wasn't sourcing meds from another
facility,'' and that ``they would also obtain'' the address and phone
number of the patient's primary physician ``so that we could call them
if there is any question as to whether'' the person was ``a legitimate
patient.'' Id. at 374.
Boswell subsequently asked Respondent if he would perform on-line
consultations for Liberty. Id. The consultations were to involve
``interview[ing] the patients'' and ``mak[ing] a recommendation'' to
prescribe drugs based ``on all the information.'' Id.
In his testimony, Respondent maintained that he asked Boswell
whether this was permissible. Id. at 375. Respondent stated that
Boswell ``assured [him] that everything was legitimate,'' that Boswell
told him that ``he was in the Armed Forces,'' and that ``he had two men
in his squad [who] were in the DEA and [that] he constantly bounced
questions off of them * * * always to make sure that he was within the
limits of the law.'' Id. Boswell also told Respondent that ``there were
certain states that did not allow internet prescribing'' and that
persons from these states would be excluded. Id. at 376.
Respondent did not, however, seek legal advice regarding the
lawfulness of Boswell's proposal. Id. at 375. Moreover, even though he
understood that he would be prescribing to patients throughout the
country, he did not undertake any inquiry on his own into the laws of
any State pertaining to the propriety of the proposed activity. Id. at
512. Instead, he concluded that Liberty was engaged in legitimate
activity because Boswell had been referred to him by his partner and
Boswell was ``concerned about making sure that everything was done
correctly,'' id. at 375, and had told him that ``he had reviewed all
the laws pertaining to this.'' Id. at 512.\2\
---------------------------------------------------------------------------
\2\ Respondent also maintained that ``to find out more'' he had
talked with another physician who performed online consultations for
Liberty. Id. at 509. Respondent did not, however, testify as to the
specifics of this conversation. Id. Respondent did not meet any of
the medical professionals who worked for Liberty and did not know
where the business was located. Id.
---------------------------------------------------------------------------
In November 2004, Respondent entered into a written contract with
Liberty; Respondent performed online consultations and prescribings for
it from approximately December 2004 through December 2005. Id. at 507.
Respondent was paid $20 per consultation and received the same fee
regardless of whether he prescribed a drug.\3\ Id. at 382-83, 508, 601.
Respondent did consultations for Liberty five days a week, and did so
every week between December 2004 and December 2005, except for three
weeks during which he took vacation. Id. at 516. Respondent performed
twenty to fifty consultations a week; he also testified that while he
was ``not exactly sure,'' he issued twenty to thirty prescriptions a
week. Id. The record is, however, unclear as to how many of the
prescriptions were for controlled substances. Id. at 568.\4\ According
to
[[Page 10085]]
Respondent, he prescribed hydrocodone, Vicodin (a schedule III
controlled substance which contains hydrocodone), and oxycodone, a
schedule II controlled substance. Id. at 547. See Physicians' Desk
Reference 526 (59th ed. 2005); see also 21 CFR 1308.12(b)(1) &
1308.13(e).
---------------------------------------------------------------------------
\3\ Respondent maintained that his compensation from Liberty was
only ``a very small part of [his] income'' and that ``it was more of
my interest in telemedicine that drove me to do it.'' Tr. 383.
Respondent testified that he was involved in a start-up company,
Technology Integrated for Medical Application (TIMA), which
conducted academic research with major institutions, and that TIMA
was developing systems to engage in medical monitoring of people
from remote locations. Id. at 505. Respondent explained that ``[w]e
can speculate that some day we'll be able to diagnose patients from
a distance where you can have a doctor in a remote location who
doesn't have the expertise in a certain area that can receive
expertise from * * * physicians in another area based on giving real
time information back to those physicians.'' Id. at 506.
\4\ Respondent testified that he prescribed both narcotics and
non-narcotics and that the estimated number of prescriptions
referred to ``all in total.'' Tr. 568. Notably, the Government
introduced no evidence showing the number of controlled-substance
prescriptions he issued during the course of his contract with
Liberty; nor did it introduce evidence showing the number of
controlled prescription he issued during a defined period of time.
---------------------------------------------------------------------------
Liberty gave Respondent a user name and password, which he used to
access PSDOCTOR, a Web-based software program which listed his
appointments; according to Respondent, he ``would call the patient and
obtain a detailed history.'' Id. at 377. Respondent testified that
through PSDOCTOR, he could retrieve patient records including a
patient's history (including the patient's complaint, what drugs the
patient was taking, what surgeries the patient had undergone, and the
patient's name and address), charts, and exams including radiological
reports. Id. at 377-78. Respondent also testified that ``sometimes [the
patients] would * * * also submit physical exams.'' \5\ Id. at 378.
---------------------------------------------------------------------------
\5\ Respondent testified that ``on the average,'' the physical
exam had to be no more than ``approximately six months'' old, but
that ``sometimes we required records more recent than six months and
sometimes patient[s] could have records up to eight months [old] or
more.'' Tr. 571. Respondent maintained, however, that in each
instance, he would have a conversation with a patient before
prescribing and that this provided ``an independent basis'' to
determine whether the patient's symptoms were continuing.'' Id. at
572.
Moreover, the ``Consent for Treatment'' forms that are in
several patient files indicate that a patient could receive the
``first prescription with an agreement that I will fax my medical
records and a photo ID * * * within 27 days and before my next
prescription is due for refill.'' RX 11, at G0156 (signed on ``12/8/
04''); RX 10, at G0151 (signed on ``12/5/05''). This suggests that
in some instances, Respondent may have issued prescriptions without
even reviewing a patient's records.
---------------------------------------------------------------------------
Respondent maintained that he would ``call the patients because
[he] want[ed] to actually talk to the patients before [he] made any
decisions on the patient,'' that ``[t]he history was very important,''
id. at 378-79, and that the calls would last an average of twenty
minutes. Id. at 615. He also testified that he performed a telephonic
consultation with every patient he prescribed to. Id. at 614-15.
Relatedly, Respondent maintained that based on his experience as a
pain doctor, he could ``get a sense of whether the patient was telling
me the truth because certain pains in certain areas elicit certain
responses.'' Id. at 379. He also testified that most patients did not
``have the savvy'' to dupe him and that ``sometimes [he] would lead
patients down the wrong path to see if they were telling the truth * *
* because there are a lot of drug seekers out there.'' Id. at 381-82.
He also stated that if a patient told him something that did not match
what was in their medical record, ``we would either call their primary
doctor'' or ``deny them.'' Id. at 382. Respondent also testified that
he ``denied a lot of patients and some of the records will show that.''
Id.
The ALJ found that some of Respondent's testimony was contradicted
in several material respects by other evidence. See ALJ at 12 (] 36).
While Respondent testified that he never prescribed without conducting
a telephone consultation with the patient, and that the consultations
lasted twenty minutes on average, Ms. A.B., who received hydrocodone
pursuant to a prescription issued by Respondent on December 8, 2004,
see GX 17, stated to a DI that within a couple of hours after she faxed
medical records to Liberty,\6\ she received a telephone call from a
doctor which lasted approximately ``one minute.'' GX 35, at 1-2. The
doctor, whose name she did not recall, asked her what her pain was. Id.
at 2. Ms. A.B. told the doctor that she had previously been treated by
a doctor in North Carolina for headaches caused by nerve damage
incurred in an automobile accident; the doctor then agreed to prescribe
for her, ninety tablets of hydrocodone/apap.\7\ Id. Ms. A.B. further
stated that the doctor did not discuss with her how her progress would
be monitored, what to do if she experienced side effects, and how to
contact him in an emergency. Id.
---------------------------------------------------------------------------
\6\ Those records included a progress note dated September 16,
2004, which indicated that A.B.'s physician had prescribed ninety
Lorcet (10/650 mg.), with no refills. RX 6, at G0050. Lorcet is a
schedule III controlled substance which combines hydrocodone with
acetaminophen. See PDR, at 1287.
\7\ Apap is an abbreviation for acetaminophen.
---------------------------------------------------------------------------
Another DI interviewed K.B., who had also obtained a combination
drug containing hydrocodone through the Liberty Web site. See GX 21;
Tr. 116-151. K.B. told the DI that she had become aware of Liberty
through a pop-up ad and that she went to the Web site and filled out a
questionnaire. Tr. 117. On August 4, 2004, K.B. sent Liberty an MRI
report showing that she had a herniated disk. Id. at 118; RX 15, at
G0190-91. ``A couple of days later,'' Tr. 118, K.B. was contacted by a
woman who stated that she was a representative of Liberty. Id.
According to K.B., the woman performed a consultation and told K.B.
that a prescription had been approved by Respondent.\8\ Id. at 118 &
131.
---------------------------------------------------------------------------
\8\ Having found that K.B. faxed a copy of the MRI report on
August 4, 2004, four months before Respondent began his contract
with Liberty, I find that Respondent did not issue the initial
prescription which K.B. received from Liberty. I do find, however,
that Respondent issued a prescription to K.B. on December 15, 2004.
See GX 21.
---------------------------------------------------------------------------
On or about December 15, 2004, K.B. received ninety tablets of
Lortab (hydrocodone/apap (10/500)), a schedule III controlled
substance, pursuant to a prescription issued by Respondent. Id. at 119-
20, GX 21; see also PDR at 3240. K.B. received approximately twenty-
five prescriptions through Liberty, the majority of which were
authorized by Respondent. Tr. 132, 141, 148, 150. K.B. never had a
conversation with Respondent, id. at 140, and had no contact with
Liberty with respect to any of the subsequent orders she placed other
than when she contacted the Web site to determine the status of an
order. Id. at 121. K.B. further told the DI that she became addicted to
hydrocodone. Id. at 122. K.B. also obtained drugs from another Web site
during a portion of the period in which she obtained drugs through
Liberty; her primary care physician did not know that she was acquiring
drugs through the internet. Id. at 120-22.\9\
---------------------------------------------------------------------------
\9\ Investigators also attempted to interview several other
persons whose names were listed on the prescription sheets found
during the trash runs. Some of the individuals could not be located,
Tr. 162 & 165, others were uncooperative. Id. at 163. Investigators
were unable to contact the persons named on the prescription labels
because the labels did not contain addresses. Id. at 169.
---------------------------------------------------------------------------
DEA Investigators also attempted to contact the persons identified
in Respondent's Exhibits 19-45, as patients who were denied
prescriptions. Tr. 470. The DIs could not contact most of the
individuals and were able to speak with only eight of them. See id. at
634-44. Of these eight persons, the record establishes that Respondent
prescribed to only one of them, Ms. S.A. See GX 26.\10\ More
specifically, on
[[Page 10086]]
December 7, 2004, Respondent prescribed to S.A. ninety tablets of
hydrocodone/apap (7.5/750 mg.).
---------------------------------------------------------------------------
\10\ For example, while a DI spoke to L.L.'s daughter (RX 20),
she did not know whether her mother ever spoke with Respondent. Tr.
635. R.T. (RX 24) stated that he never received drugs from Liberty,
Tr. 637, and there is no evidence to the contrary. While M.A. stated
that he did not speak with Respondent, id. at 637-38, documentary
evidence indicated that Respondent did not issue a prescription
because he felt that M.A. ``IS WANTING MEDS FOR SOMEONE ELSE.'' RX
26. Again, there is no evidence establishing that Respondent issued
a prescription to M.A.
A.F. (RX 27) acknowledged taking Vicodin and sending medical
records somewhere. Tr. 638. He did not, however, remember where,
id.; and in any event, there is no evidence that Respondent
prescribed to him. M.K. (RX 31) acknowledged receiving hydrocodone
from Liberty ten times, that he received his first order without a
consultation, and that his ``subsequent orders usually did involve a
two to three minute conversation with someone claiming to be a
physician or a physician's assistant.'' Tr. 640. Again, there is no
evidence establishing that Respondent (as opposed to other doctors
who worked for Liberty) prescribed to him. RX 31.
M.B. (RX 33) acknowledged that he received hydrocodone from
Liberty four times and ``recalled talking to someone at the Liberty
Meds Web site but [did not] remember who.'' Tr. 641. K.K. (RX 36)
acknowledged ordering hydrocodone ``four or five'' times, but
identified a different doctor as the prescriber. Tr. 641-42.
Similarly, T.A. (RX 37) stated that he had ordered hydrocodone from
Liberty ``two or three'' times, and that he had conversations with
either a doctor or physician's assistant lasting ``two to three
minutes,'' but could only identify a different doctor as the person
he spoke to. Id. at 642. As above, there is no evidence establishing
that Respondent prescribed to either M.B. or T.A.
---------------------------------------------------------------------------
Ms. S.A. stated that she ordered hydrocodone from Liberty ``at
least ten times and that she did not speak to any physician on the
first two occasions.'' \11\ Tr. 643. S.A. further stated that on
subsequent orders, she had ``very short conversations lasting
approximately one minute or less,'' but could not recall the name of
any person she had talked to. Id. at 643-44.
---------------------------------------------------------------------------
\11\ Here again, the evidence shows that S.A. faxed her records
to Liberty on August 25, 2004, four months before Respondent began
his contract with Liberty. RX 7, at G0113-14.
---------------------------------------------------------------------------
Respondent testified that S.A.'s medical record supported the
prescription he issued and that the drug and dosage he prescribed was
appropriate for her condition. Tr. 451. Yet the evidence suggests that
the most recent medical report available to Respondent was an
``Operative Report'' for a procedure which had been performed nearly
eight months earlier. See RX 7, at G0112. Moreover, Respondent offered
no explanation as to why S.A.'s condition was of such a nature as to
justify prescribing based on an eight-month-old report.
A DI also interviewed R.Z., to whom Respondent prescribed 90
tablets of Vicodin ES (7.5/750 mg.), on January 5, 2005. GX 18. R.Z.
told the DI that she had become aware of Liberty in approximately
November 2004; someone at Liberty put R.Z. in contact with a man ``who
claimed to be a doctor.'' Tr. 72. R.Z. could not, however, remember the
name of the doctor, but did recall having a phone conversation of
``approximately ten minutes'' duration with him in which she was asked
questions about her condition, what type of pain she had, what type of
pain medication she needed, how she tolerated pain medications, and her
blood pressure. Id. at 73. The doctor then told R.Z. that he would
prescribe to her ninety tablets of Vicodin. Id. at 74. R.Z. also told
the DI that she had faxed to Liberty an x-ray report which showed that
she had a bulging disk.\12\ Id. R.Z. further told the DI that she had
received from Liberty monthly prescriptions for ninety tablets of
Vicodin over ``a thirteen to fourteen-month period.'' \13\ Id. at 77-
78.
---------------------------------------------------------------------------
\12\ R.Z. stated that she had sent in only the x-ray report and
filled out an online questionnaire. Tr. 89. R.Z. was never directed
to obtain further tests (such as a new x-ray), and stated that she
did not believe that Liberty ever contacted her primary doctor. Id.
at 79, 89-90.
\13\ R.Z. also stated that she had conversations every three to
four months regarding her condition with a woman from Liberty who
claimed to be a physician. Tr. 76, 87. R.Z. testified that she had a
single conversation with a male caller. Id. at 96.
---------------------------------------------------------------------------
Respondent testified that the prescription he issued was consistent
with the findings contained in the x-ray report. Id. at 459; RX 10, at
G0154. The x-ray report contains the notations: ``Record Received on 1/
31/05,'' and ``Verified on 1/31/05 By MW.'' Id. In addition, the record
includes a handwritten note dated ``1/31/05,'' which states in relevant
part: ``Attention Leisha, Here are the results of the xray I had on my
back. * * * I would like my refill sent when it becomes time to do
so.'' Id. at G0153. Respondent further testified that ``I don't see a
physical exam here but it would be something that we would require.''
Tr. 459. He also maintained that in order for R.Z. to get an x-ray,
``she had to have some history,'' because ``you can't refer yourself
for an x-ray.'' Id.
Even so, that a patient needs a referral to obtain an x-ray, does
not establish that Respondent reviewed R.Z.'s history and a physical
exam report before he prescribed to her. Indeed, the absence of a
physical exam report in R.Z.'s file is consistent with her statement
that she sent in only the x-ray report. See Tr. 89. I therefore find
that contrary to Respondent's testimony, he did not review a physical
exam report before prescribing to R.Z.\14\
---------------------------------------------------------------------------
\14\ The ALJ noted that it ``is unclear * * * whether or not the
Respondent had access to, or actually reviewed medical records prior
to prescribing controlled substances to any of Liberty's customers
discussed at the hearing.'' ALJ at 19 n.10. While this is correct
with respect to some patients, with respect to R.Z., it is clear
that Respondent prescribed without having any medical records that
supported the prescription.
In the context of discussing his prescribing through Liberty,
Respondent also testified that ``I will always'' have some ``data''
and ``I won't just place them on a prescription.'' Tr. 442. Perhaps
Respondent was testifying about his prescribing practices at the
time of the hearing. Or perhaps he considered the answers Liberty's
customers gave to the questionnaires to be ``data.'' In any event,
the evidence establishes that he prescribed to R.Z. without either
reviewing a physical exam report or the x-ray report.
---------------------------------------------------------------------------
As for Respondent's statement that the Vicodin prescription he
issued to R.Z. was consistent with the findings of the x-ray report,
the evidence shows that he issued the prescription on January 5, 2005,
nearly four weeks before Liberty received the x-ray report. Respondent
therefore could not have issued the prescription on the basis of the
report.
With respect to K.B. (whose interview with a DI is described
above), Respondent also maintained that a report for an MRI which had
been done ten months earlier, see RX 15, at G0190; established that the
hydrocodone prescription he issued was appropriate. Tr. 467. Respondent
then testified that Respondent ``had been on Toradol and Ultram and had
not received results.'' Id. Continuing, Respondent stated that ``[s]he
also had gotten Lortab it seems. If you look at G0195, in the middle
where it says 2/19/04, it says renewed her Lortab and Flexeril.'' Id.
at 467-68.
Notably, both pages G0194 and G0195, which appear to contain
progress notes of various visits K.B. made to an orthopedic clinic
between January 15, 2003, and November 29, 2004, have the notations:
``Record Received on 1/31/05,'' and ``Verified on 1/31/05 By MW.'' RX
15, at G0194-95. Moreover, each page has a header indicating that it
was faxed on January 31, 2005. See id. As found above, Respondent
issued the prescription to K.B. on December 15, 2004, approximately six
weeks before these documents were faxed to Liberty. GX 21. Here again,
Respondent could not have relied on the documents when he issued the
prescription to K.B., notwithstanding his testimony that ``we would
require'' a physical exam. Tr. 459.\15\
---------------------------------------------------------------------------
\15\ As found above, Respondent never spoke with K.B. Tr. 140.
During the period she was obtaining controlled substances from
Liberty, K.B. was under the care of another physician; K.B.,
however, never told the latter physician that she was receiving
drugs from Liberty. Id. at 122, 142-43.
Respondent maintained that Liberty was ``unable to provide all
the records'' because of problems it was having with its ``IT
person.'' Tr. 410. However, the files for some of the patients
appear extensive, see RXs 3 (22 pages), 5 (18 pages), 6 (64 pages),
7 (17 pages), & 14 (23 pages), thus prompting the question of why
Liberty was able to provide so much documentation for these patients
but not for some of the others. Moreover, the patient files indicate
that the patients almost always faxed or mailed their records to
Liberty. Thus, even if the records were scanned into Liberty's
computer system, Respondent offered no evidence to establish what
happened to the original records. Finally, there is no evidence that
Respondent requested a subpoena for the records. While the ALJ
apparently found that Respondent credibly testified that he did not
receive all of the information he requested, ALJ Dec. at 13 n.3., I
conclude that the patient files Respondent introduced into evidence
fairly reflect the patient files as obtained by Liberty.
The ALJ further reasoned that Respondent's testimony supported
``the requirement that [he] maintain his own patient records.'' Id.
It is further noted that under the New Jersey Board of Medical
Examiners' regulation which governs the prescribing of controlled
substances, ``[t]he practitioner shall keep accurate and complete
records.'' N.J. Adm. Code 13:35-7.6(g) (emphasis added). There is,
however, no requirement under federal law that an ``individual
practitioner * * * keep records of controlled substances in
Schedules II, III, IV, and V which are prescribed in the lawful
course of professional practice, unless such substances are
prescribed in the course of maintenance or detoxification treatment
of an individual.'' 21 CFR 1304.03. I do not decide whether it was
permissible under the New Jersey regulation for Respondent to
maintain medical records through the Liberty Web site.
---------------------------------------------------------------------------
[[Page 10087]]
Other Patients
On January 5, 2005, Respondent issued a prescription to K.A., a
Texas resident, for ninety tablets of hydrocodone/apap (10/500mg). GX
27. The record contains extensive progress notes showing that K.A. was
being treated by a San Antonio, Texas pain management specialist during
2004 and 2005 for neck pain.\16\ See RX 3. Respondent testified that
K.A. ``has various different problems * * * that would cause one to
have a ton of severe pain.'' Tr. 426. Respondent testified that based
on his review of the record, the medication and dosage he prescribed
was appropriate. Id. at 432. Respondent offered no testimony, however,
as to whether he contacted the pain management specialist who was
treating K.A. See generally id. at 426-32.
---------------------------------------------------------------------------
\16\ Based on the progress notes as well as K.A.'s Texas
driver's license, I find that K.A. was a resident of Texas. See RX
3, at G0001.
---------------------------------------------------------------------------
On December 20, 2004, Respondent prescribed to P.G., a Minnesota
resident, ninety tablets of hydrocodone/apap (10/500 mg.) with one
refill. GX 19. Although the most recent progress note in P.G.'s record,
which was dated April 13, 2004, indicated that he had ``[c]hronic low
back with right lower extremity radicular pain,'' and that his local
physician had issued him a prescription for twenty tablets of Percocet
p.r.n., P.G.'s physician further observed that ``[l]ong-term use of
narcotics for back pain is not in his best interest and therefore he is
given only 20 tablets at this time.'' RX 4, at G0024. While Respondent
testified that his prescription was appropriate, Tr. 435, when asked on
cross-examination whether the eight-month-old progress note was of
sufficient recency to make a diagnosis, he testified: ``It really
depended also on the patients and the physical findings but this does
seem like it was two months later than we usually accept. * * *'' Id.
at 525.
On January 5, 2005, Respondent prescribed to D.C., a resident of
Georgia, ninety tablets of hydrocodone/apap (10/325 mg.). GX 24. The
most recent progress note in her file prior to this prescribing was
dated June 24, 2004, and indicated that the physician's impression was:
``Probable right C7 radiculopathy.'' RX 5, at G0035. When asked by his
counsel whether this would ``indicate that pain should be in a
particular area?,'' Respondent answered: ``Yes, she should have the
pain in the right upper extremity. If I had spoken with this person
about giving her a treatment, I would have first tried to elicit where
her pain was coming from.'' Tr. 437 (emphasis added). Respondent then
discussed the findings of a physical exam which occurred on April 21,
2005, and which he obviously could not have relied on when he issued
the prescription three months earlier. See id. at 437-38.
Next, Respondent maintained that he would try to confirm with the
patient whether their reported pain matched with ``what it should be.''
Id. at 439. He also maintained that his prescribing was consistent with
the drug (Vicodin 7.5) that the physician, who physically examined her
three months later, had prescribed. Id. at 440; RX 5, at G0032.
On cross-examination, Respondent acknowledged that while the
medical records showed that D.C. had been by an orthopedist and
neurologist, neither had referred her to him. Tr. 527. When asked what
his treatment plan was for D.C., Respondent could not recall. Id. He
also did not refer her to a pain clinic near where she lived. Id. at
528.
On December 15, 2004, Respondent prescribed to S.K., a resident of
Texas, ninety tablets of hydrocodone/apap (10/325mg.), with one refill.
GX 22. Again, Respondent testified that the prescription he wrote
``would be consistent with what she's experiencing on physical exam
here.'' Tr. 454. While Respondent testified that S.K.'s records ``were
accessed through PSDoctor,'' id. at 455; the only medical exam report
in S.K.'s file is dated ``6/1/05,'' and was faxed on June 10, 2005. See
RX 8, at G0129-31. Respondent therefore could not have relied on the
report in issuing the prescription.
On January 6, 2005, Respondent prescribed to S.B., a South Carolina
resident, ninety tablets of Lortab (10/500mg.). GX 27. SB's patient
file contains only three documents: a copy of her driver's license, a
``consent for treatment'' form dated ``12/8/04,'' and the results of a
blood test taken on October 28, 2003. See RX 11. Respondent maintained
that S.B.'s file was ``incomplete,'' and that ``she would'' have been
asked to provide other data. Tr. 460. The ALJ did not, however, make
any findings regarding the credibility of Respondent's testimony
pertaining to S.B. In light of the other instances in which Respondent
prescribed even though a patient's file was missing information, I find
that it is more likely than not that he prescribed to S.B. without
obtaining any additional medical documentation.
On January 5, 2005, Respondent prescribed to K.S., a resident of
Texas, ninety tablets of hydrocodone/apap (10/500) with one refill. GX
29. K.S.'s records include extensive progress notes which show that she
had last been seen by a physician on September 28, 2004, and had last
been prescribed a controlled substance (codeine/apap) on December 20,
2004. RX 14, at G0182.
Respondent testified that ``[i]t seemed like she had really good
follow-up here according to these progress notes,'' Tr. 462-63, and
that the prescription he wrote ``would be appropriate for'' the
condition documented in the record. Id. at 465. Respondent offered no
explanation as to why he was prescribing to a patient who had received
a controlled substance prescription from another physician only two
weeks earlier. Moreover, given his acknowledgment that K.S.'s records
showed that she was receiving good follow-up care, he offered no
testimony that he had contacted K.S.'s physician to coordinate her care
and ensure that she was not engaged in doctor shopping.\17\
---------------------------------------------------------------------------
\17\ K.S.'s file includes a letter which forwarded some records
to Liberty. On the letter, there is a handwritten notation that the
records had been reviewed, but that the clinic, which treated K.S.,
was ``closed for lunch.'' RX 14, at G0170.
---------------------------------------------------------------------------
On January 3, 2005, Respondent prescribed ninety tablets of
hydrocodone/apap (10/325 mg.) to E.M., a New Hampshire resident.\18\
Beside two copies of E.M.'s driver's license, her patient file contains
two forms: (1) A Family and Medical Leave Act certification that E.M.
had a serious illness, and (2) an Office of Workers Compensation
Programs' form documenting a medical examination (performed on October
1, 2004) and diagnosis and supporting the need for certain restrictions
on E.M.'s work-related duties. See RX 16 at G0200-01. The latter form
indicates that E.M. had low back pain and tendonitis in her hand and
shoulder. Id. at G0201. The form, however, contains no
[[Page 10088]]
documentation of her vital signs. See id. Moreover, when asked by his
counsel whether the prescription he issued to E.M. was appropriate,
Respondent answered that ``we do prescribe medicine for'' tendonitis
and carpal tunnel, but that ``it seems like this chart is incomplete,''
Tr. 469, and that ``[i]t might have been missing EMGs or other
things.'' Id. at 536. He again testified that it was his practice to
look for other data before prescribing such as ``radiographic or
EMGs.'' Id. at 537. While Respondent acknowledged that E.M.'s record
did not have any such data, he then maintained that ``this might be an
incomplete record.'' Id.
---------------------------------------------------------------------------
\18\ While the ALJ found that E.M. was a Texas resident, ALJ at
27 (FOF 90), RX 16 includes copies of E.M.'s driver's license which
appears to indicate that she was a New Hampshire resident. Moreover,
the fax header indicted that the documents were faxed to Liberty
from a phone number with a 603 area code, which is an area code for
New Hampshire.
The ALJ also noted that the prescription label (GX 29) was dated
``1/3/04.'' ALJ at 27 n.18. Based on the undisputed evidence that
Respondent did not commence working for Liberty until December 2004,
the ALJ found that the actual date of the prescription was January
3, 2005. Id.; see also Tr. 535. I adopt this finding.
---------------------------------------------------------------------------
Yet several of the documents contained in E.M.'s patient file
indicate that they were faxed to Liberty on December 31, 2004. Id. at
G0202-03.\19\ Again, Respondent offered no credible explanation as to
why E.M's file as turned over to him had these documents (which Liberty
obtained shortly before he issued the prescription to her) but not the
others which ``might have been missing.'' Id. at 536. I therefore find
that there were no such additional documents in E.M.'s patient file
when he prescribed to her.
---------------------------------------------------------------------------
\19\ Again, while Respondent testified that the records that he
requested from Liberty were incomplete, he offered no explanation as
to why Liberty was able to provide some records for a patient but
not the missing ones. Moreover, the evidence indicates that many of
the patients faxed their records to Liberty. Even if these records
were scanned into a database, Respondent offered no evidence as to
what became of the original documents.
---------------------------------------------------------------------------
On December 15, 2004, Respondent issued to L.F., a resident of New
Jersey, a prescription for ninety tablets of hydrocodone/apap (7.5/
750mg.) with one refill. GX 23. Respondent testified that L.F.'s
records showed that his physician ``did a physical exam,'' and that
``[t]here is also one on 10/8/04 by the same physician which was
consistent with what was found on 10/8/03, * * * you can see the same
vertebral bodies marked off, so it's very consistent with what the
patient is having.'' Tr. 456. Respondent maintained that L.F. had a
condition which ``merit[ed] intervention for pain,'' id., and that the
dosage he prescribed was consistent with his condition. Id. at 457.
On cross-examination, the Government asked Respondent to compare
the handwriting of the two reports of ``Examination Findings,'' which
were dated ``10/8/03'' and ``10/8/04'' respectively. Id. at 530; see
also RX 9, at G0142 & G0145. Respondent acknowledged that ``[a]ll the
handwriting [on the two reports] is in exactly the same position.'' Tr.
530. Respondent testified, however, that when he prescribed to L.F., he
``did not'' recognize that one of the documents had probably been
falsified. Id. Moreover, none of the documents in L.F's file contained
his vital signs. See RX 9. And as with the other Liberty patients,
Respondent did not physically examine L.F., even though he lived in
northern New Jersey, and near where he practiced.\20\ See id. at G0147,
GX 23.
---------------------------------------------------------------------------
\20\ Respondent practiced pain management at a clinic in
Livingston, New Jersey. RX 1; ALJ at 5. L.F. lived in Wallington,
and L.W. lived in Warren, New Jersey. RXs 20 & 23. In accordance
with 5 U.S.C. Sec. 556(e), I take official notice of the fact that
all three of these cities are located in northern New Jersey. See 5
Rand McNally, Business Traveler's Road Atlas 62, 68-69 (1994).
Notwithstanding the proximity of his clinic to L.F.'s and L.W.'s
residences, Respondent did not require them to appear for a physical
examination.
An agency ``may take official notice of facts at any stage in a
proceeding--even in the final decision.'' U.S. Dept. of Justice,
Attorney General's Manual on the Administrative Procedure Act 80
(1947). In accordance with the Administrative Procedure Act and
DEA's regulation, Respondent is ``entitled on timely request to an
opportunity to show to the contrary.'' 5 U.S.C. 556(e); see also 21
CFR 1316.59(e). Accordingly, Respondent may file a motion for
reconsideration within fifteen days of service of this order which
shall commence with the mailing of the order.
---------------------------------------------------------------------------
On December 7, 2004, Respondent prescribed to L.W., another New
Jersey resident, ninety tablets of hydrocodone/apap (10/325 mg.) with
one refill. GX 20. L.W.'s patient file consisted of three pages: a
progress note dated June 17, 2004, a sheet indicating that L.W. was
faxing her driver's license, and a blurred copy of a driver's license.
See RX 12. The progress note lists several diagnostic codes and under
the handwritten notation of ``CODES,'' states: ``polycystic ovaries,''
``adhesions,'' and ``pelvic pain.'' RX 12, at G0158. Next to the column
for history, the document includes a notation of ``Percocet
120.'' Id.
With respect to L.W., Respondent maintained that ``[t]hese patients
have pelvic pain generally to the lower abdomen.'' Tr. 461. Respondent
then testified that ``[t]here is no radiological exam that you would do
to tell you anything differently[,] [b]ut obviously they know she has
polycystic ovaries according to this physician's history and
physical.'' Id. Respondent testified that the prescription was
appropriate for a patient with this condition, and that he believed
someone had verified L.W.'s identity with her physician because ``her
license was blurred.'' Id. Respondent did not, however, testify that he
called Respondent's physician.
Respondent's Other Evidence
Respondent also testified that he had proposed that Liberty use a
narcotic contract under which a patient was required to agree not to
give or sell his drugs to others, as well as not to seek drugs from
other physicians. Tr. 384; see also RX 11, at G0156. According to the
contract, a patient would be dismissed for failing to comply. Tr. 384.
Yet Respondent was not ``sure how'' Liberty determined whether a
patient was obtaining drugs from other sources such as another Web
site. Id. at 385.
Respondent gave conflicting testimony as to whether he had
prescribed oxycodone to Liberty's patients. First, he testified that he
did so at a frequency that was ``pretty much equal'' to that of his
hydrocodone prescribing. Id. at 585. Later, however, when Respondent
was asked by the ALJ as to whether he ever recalled prescribing
schedule II controlled substances to a Liberty patient, he appeared to
backtrack from this testimony answering: ``Yes, there was a patient in
our system you mean.'' Id. at 605.\21\
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\21\ The ALJ also found that Respondent authorized refills of
schedule II controlled substances and that he ``was unaware of the
forms needed to actually prescribe a schedule II controlled
substance.'' ALJ 14 (citing Tr. 604-05). Respondent testified,
however, that he was not ``aware of'' ``a requirement for a Schedule
II substance to be prescribed on a specifically identified form.''
Tr. 605.
Except for in an emergency situation, the dispensing of a
schedule II controlled substance requires ``a written prescription
signed by the practitioner,'' and the ``original written, signed
prescription [must be] presented to the pharmacist for review prior
to the actual dispensing of the controlled substance.'' 21 CFR
1306.11(a). However, no special form is required to prescribe a
schedule II drug and Respondent's testimony was correct. Federal law
does, however, prohibit the refilling of a schedule II controlled
substance. 21 U.S.C. 829(a).
---------------------------------------------------------------------------
Respondent further testified that he believed that his prescribing
practices complied with New Jersey's regulations and were consistent
with a 2001 DEA Guidance Document. With respect to the New Jersey
regulation, which provides that ``a practitioner shall not dispense
drugs or issue prescriptions to an individual, * * * without first
having conducted an examination, which shall be appropriately
documented in the patient record,'' except for in six defined
circumstances, N.J. Admin Code Sec. 13:35-7.1A, Respondent testified
that exceptions three (``[f]or continuation medications on a short term
basis for a new patient prior to the patient's first appointment'') and
four (``[f]or an established patient who, based on sound medical
practice, the physician believes does not require a new examination
before issuing a new prescription''), ``could apply.'' Tr. 589; see
also N.J. Admin. Code Sec. 13:35-7.1A(b)(3) & (4). Respondent did not,
however, identify any patient he prescribed to over the
[[Page 10089]]
Internet who later came in for an appointment. Nor did he testify that
any of the persons whose names were found on the prescription sheets
and labels was an established patient.
Respondent also maintained that his Internet prescribing was
consistent with the statements in this Agency's Guidance Document,
Dispensing and Purchasing Controlled Substances Over the Internet, 66
FR 21181 (2001). More specifically, Respondent maintained that his
practices were consistent with the Guidance Document because ``[w]e
always had the patient's chief complaint, history was taken, a physical
examination was done by another physician, and we collected all the
evidence together and then I made my decision based on all the evidence
including the radiographical evidence.'' Tr. 417. Respondent further
maintained that ``it was not'' his practice to prescribe based solely
on Internet correspondence. Id.
Finally, Respondent's counsel read to him the following question
and answer from the Guidance Document:
I am a Physician. Does the need for a Physical Exam Mean that I
Cannot Engage in Telemedicine and Prescribe Controlled Substances?
No, DEA does not intend to limit the ability of doctors to
engage in telemedicine. If the patient cannot travel to your office,
but you supervise an exam given by a nurse or other professional,
you can then prescribe the needed medications based on the results,
to the extent that State law allows. In this case, your decision on
the appropriateness of the medication is based on facts (symptoms,
blood pressure, etc.) that have been verified by a qualified third
party and observed by you electronically.
GX 6, at 5; Tr. 418.\22\
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\22\ At the hearing, Respondent's counsel slightly altered the
text of the answer published in the Guidance Document. The
alteration did not, however, materially change the meaning of the
answer.
---------------------------------------------------------------------------
Respondent was then asked by his counsel whether his Internet
practice was consistent with this statement. Tr. 418-19. Respondent
answered: ``Yes. In fact, we've exceeded those, also communicating with
the physicians, not just electronically but via telephone.'' Id. at
419. Respondent then explained that ``the radiographical reports were
read by a physician radiologist, the physical exams were done by
another physician, so sometimes we have a couple of physicians involved
in the process. Id.\23\
---------------------------------------------------------------------------
\23\ Respondent also testified that the first time he saw the
2001 Guidance Document was at the hearing. Tr. 522.
---------------------------------------------------------------------------
Respondent did not, however, identify a single instance in which he
supervised and observed a physical exam as it was being performed by
another qualified medical professional. Moreover, Respondent did not
have any recollection as to having spoken to any of the physicians who
were identified in the patient records that were introduced into
evidence in this proceeding. Id. at 573. Finally, he was unaware as to
whether any of the patient notes he made were ever sent by Liberty to
the primary care physicians of those he prescribed to. Id. at 614. He
also never gave written referrals for Liberty patients to see local
doctors. Id. at 512.
Respondent testified that he had stopped performing telemedicine
consultations for Liberty in late December of 2005. Id. at 487. He also
represented that it was not his ``present intention'' to resume
internet based prescribing. Id.
As noted above, Respondent introduced into evidence a number of
printouts from Liberty's software with the heading ``Patient
Information for Appointment.'' See RXs 19-45. These printouts establish
that in several instances, patients were denied drugs because they were
receiving them from other sources. See RXs 19, 21, 27, 32, 33, 39.
Moreover, in other instances Respondent did not approve a prescription,
see RX 23, 34, 43; and in at least one case, Respondent denied a
prescription because he felt the person ``was wanting meds for someone
else.'' RX 26. Moreover, the printouts suggest that in other instances,
either Liberty or Respondent denied requests because the person was
seeking the drugs too soon, RX 22, 35, 36; the patient's records had
not been verified, RX 28; or the patient needed to be evaluated and
send in records before Respondent approved a refill. RX 42 & 44. Only
one of these printouts, however, corresponds with a patient (S.A.) who
was identified above as having received a prescription which was issued
by Respondent.\24\ Compare RX 44 with GX 26.
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\24\ The National Center on Addiction and Substance Abuse (CASA)
has reported that ``[t]he number of people who admit abusing
controlled prescription drugs increased from 7.8 million in 1992 to
15.1 million in 2003.'' National Center on Addiction and Substance
Abuse, Under the Counter: The Diversion and Abuse of Controlled
Prescription Drugs in the U.S. 3 (2005) (GX 3). Moreover,
``[a]pproximately six percent of the U.S. population (15.1 million
people) admitted abusing controlled prescription drugs in 2003, 23
percent more than the combined number abusing cocaine (5.9 million),
hallucinogens (4.0 million), inhalants (2.1 million) and heroin
(328,000).'' Id. Relatedly, ``[b]etween 1992 and 2003, there has
been a * * * 140.5 percent increase in the self-reported abuse of
prescription opioids''; in the same period, the ``abuse of
controlled prescription drugs has been growing at a rate twice that
of marijuana abuse, five times greater than cocaine abuse and 60
times greater than heroin abuse.'' Id. at 4.
CASA has further reported that teenagers ``represent an
especially vulnerable group,'' because ``[t]eens may view
prescription drugs as relatively safe either when abused alone or in
combination with alcohol or other drugs.'' Id. According to CASA,
``[i]n 2003, 2.3 million teens ages 12 to 17 (9.3 percent) reported
abusing a controlled prescription drug in the past year; 83 percent
of them reported abusing opioids.'' Id. Moreover, ``[b]etween 1992
and 2002, the number of [first time] teenage prescription opioid
abusers increased by 542 percent.'' Id. at 35.
Finally, CASA noted that ``[i]nternet sites not adhering to
state licensing requirements, medical board standards or federal law
have enabled consumers to obtain controlled prescription drugs
without a valid prescription or physician supervision and without
regard to age.'' Id. at 63. CASA also noted that ``illegal
[i]nternet pharmacies have introduced a new avenue through which
unscrupulous buyers and users can purchase controlled substances for
unlawful purposes.'' Id. Moreover, ``[t]he age of the customers
appears not to be an issue for Internet pharmacies,'' and that there
are ``no mechanisms in place to block children from purchasing
controlled drugs over the Internet.'' Id. at 66.
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Discussion
Section 304(a) of the Controlled Substances Act (CSA) provides that
a registration to ``dispense a controlled substance * * * may be
suspended or revoked by the Attorney General upon a finding that the
registrant * * * has committed such acts as would render his
registration under section 823 of this title inconsistent with the
public interest as determined under such section.'' 21 U.S.C.
824(a)(4). With respect to a practitioner, the Act requires the
consideration of the following factors in making the public interest
determination:
(1) The recommendation of the appropriate State licensing board
or professional disciplinary authority.
(2) The applicant's experience in dispensing * * * controlled
substances.
(3) The applicant's conviction record under Federal or State
laws relating to the manufacture, distribution, or dispensing of
controlled substances.
(4) Compliance with applicable State, Federal, or local laws
relating to controlled substances.
(5) Such other conduct which may threaten the public health and
safety.
Id. section 823(f).
``[T]hese factors are * * * considered in the disjunctive.'' Robert
A. Leslie, M.D., 68 FR 15227, 15230 (2003). I ``may rely on any one or
a combination of factors, and may give each factor the weight [I]
deem[] appropriate in determining whether a registration should be
revoked.'' Id. Moreover, I am ``not required to make findings as to all
of the factors.'' Hoxie v. DEA, 419 F.3d 477, 482 (6th Cir. 2005); see
also Morall v. DEA, 412 F.3d 165, 173-74 (D.C. Cir. 2005).
In this matter, it is undisputed that neither the State of New York
nor the
[[Page 10090]]
State of New Jersey has taken action against Respondent's medical
license (factor one). It is also undisputed that Respondent has not
been convicted of an offense related to controlled substances under
federal or state law (factor three).\25\ This proceeding focused,
however, on Respondent's experience in dispensing controlled substances
and his record of compliance with applicable laws. As discussed below,
the evidence pertaining to these factors is disturbing and
establishes--at a minimum--that Respondent committed numerous
violations of both Federal and state laws.
---------------------------------------------------------------------------
\25\ Under settled precedent, neither of these factors is
dispositive. See Edmund Chein, 72 FR 6580, 6590 n.22 (2007);
Mortimer B. Levin, 55 FR 8209, 8210 (1990).
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Factor Two and Four--Respondent's Experience in Dispensing Controlled
Substances and Record of Compliance With Applicable Controlled
Substance Laws
Under a longstanding DEA regulation, a prescription for a
controlled substance is not ``effective'' unless it is ``issued for a
legitimate medical purpose by an individual practitioner acting in the
usual course of his professional practice.'' 21 CFR 1306.04(a). This
regulation further provides that ``an order purporting to be a
prescription issued not in the usual course of professional treatment *
* * is not a prescription within the meaning and intent of [21 U.S.C.
829] and * * * the person issuing it, shall be subject to the penalties
provided for violations of the provisions of law relating to controlled
substances.'' Id. As the Supreme Court recently explained, ``the
prescription requirement * * * ensures patients use controlled
substances under the supervision of a doctor so as to prevent addiction
and recreational abuse. As a corollary, [it] also bars doctors from
peddling to patients who crave the drugs for those prohibited uses.''
Gonzales v. Oregon, 546 U.S. 243, 274 (2006) (citing United States v.
Moore, 423 U.S. 122, 135 (1975)).
Under the CSA, it is fundamental that a practitioner must establish
a bonafide doctor-patient relationship in order to act ``in the usual
course of * * * professional practice'' and to issue a prescription for
a ``legitimate medical purpose.'' Moore, 423 U.S. at 141-43. The CSA,
however, generally looks to state law to determine whether a doctor and
patient have established a bonafide doctor-patient relationship. See
Kamir Garces-Mejias, 72 FR 54931, 54935 (2007); United Prescription
Services, Inc., 72 FR 50397, 50407 (2007); Dispensing and Purchasing
Controlled Substances Over the Internet, 66 FR at 21182-83.\26\
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\26\ On October 15, 2008, the President signed into law, the
Ryan Haight Online Pharmacy Consumer Protection Act of 2008, Pub. L.
110-425, 122 Stat. 4820 (2008). Section 2 of the Act prohibits the
dispensing of a prescription controlled substance ``by means of the
Internet without a valid prescription,'' and defines, in relevant
part, the ``[t]he term `valid