Jose Gonzalo Zavaleta, M.D.; Denial of Application, 49506-49508 [2011-20284]
Download as PDF
49506
Federal Register / Vol. 76, No. 154 / Wednesday, August 10, 2011 / Notices
U.S. Department of Justice, Washington,
DC 20044–7611. When requesting a
copy by mail, please enclose a check
payable to the U.S. Treasury in the
amount of $29.25 (25 cents per page
reproduction cost). A copy may also be
obtained by e-mailing or faxing a
request to Tonia Fleetwood,
tonia.fleetwood@usdoj.gov, fax number
(202) 514–0097, phone confirmation
number (202) 514–1547, and mailing a
check for the reproduction cost to the
Consent Decree Library.
Robert E. Maher, Jr.,
Assistant Section Chief, Environmental
Enforcement Section, Environment and
Natural Resources Division.
[FR Doc. 2011–20321 Filed 8–9–11; 8:45 am]
BILLING CODE 4410–15–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
emcdonald on DSK2BSOYB1PROD with NOTICES
Jose Gonzalo Zavaleta, M.D.; Denial of
Application
On February 23, 2009, the Deputy
Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration, issued an Order to
Show Cause (Order) to Jose Gonzalo
Zavaleta, M.D. (Applicant), of Pineville,
Louisiana. The Order proposed the
denial of Applicant’s pending
application for a DEA Certificate of
Registration as a practitioner, on the
ground that his registration would be
‘‘inconsistent with the public interest.’’
Order at 1 (citing 21 U.S.C. 823(f)).
The Order alleged that Applicant
voluntarily surrendered his DEA
Certificate of Registration, BZ5998250,
on March 26, 2008, after being charged
with six counts of prescribing controlled
substances beyond authority and
accepted medical treatment, in violation
of La. Rev. Stat. Ann. § 40:971
(C)(1)(2008) (effective Aug. 15, 2006). Id.
The Order further alleged that Applicant
prescribed controlled substances to
undercover agents with ‘‘cursory or no
medical examinations, and without a
legitimate medical purpose in violation
of 21 U.S.C. 841(a)(1).’’ Id. More
specifically, the Order alleged that
Applicant prescribed a total of 75
dosage units of hydrocodone (including
Lortab and/or Lorcet), which are
schedule III narcotics; 20 dosage units of
Xanax, a schedule IV controlled
substance; and six ounces of Phenergan
with codeine, a schedule V narcotic
cough syrup. Id. Finally, the Order that
alleged ‘‘[Applicant] facilitated the
undercover officers’ procurement of
drugs by fraudulent means’’ when he
advised them to ‘‘provide false medical
VerDate Mar<15>2010
17:48 Aug 09, 2011
Jkt 223001
information’’ to justify ‘‘illegitimate
prescriptions.’’ Id. at 2.
On March 2, 2009, the Order, which
also notified Applicant of his right to
either request a hearing on the
allegations or to submit a written
statement in lieu of a hearing, the
procedures for doing so, and the
consequence if he failed to do so, was
served on Applicant by certified mail
addressed to him at the address listed
on his application. Id. at 2 (citing 21
CFR 1316.47; 21 CFR 1301.43). Since
service of the Order, more than thirty
days have now passed and neither
Applicant, nor anyone purporting to
represent him, has either requested a
hearing or submitted a written statement
in lieu of a hearing. See 21 CFR
1301.43(b)–(d). Accordingly, I find that
Applicant has waived his rights to a
hearing or to submit a written statement.
Id. 1301.43(d). I therefore issue this
Decision and Final Order without a
hearing based on relevant material
contained in the investigative record
submitted by the Government. I make
the following findings.
Findings
Applicant was previously the holder
of DEA Certificate of Registration,
BZ5998250, which authorized him to
dispense controlled substances in
schedules II through V as a practitioner
at the registered location of 5629
Jackson Street Ext, Alexandria,
Louisiana. Affidavit of Diversion
Investigator (hereinafter, DI Aff.), at 1;
Applicant Registration Information, at 1.
However, on March 26, 2008,
concurrent with Applicant’s arrest on
state drug charges (the circumstances of
which are set forth below), he
voluntarily surrendered his registration.
DI Aff., at 1. Applicant’s registration
was then retired by DEA on March 27,
2008. Applicant Registration
Information, at 1. On July 28, 2008,
Applicant applied for a new DEA
registration as a practitioner in
schedules IV and V. Id.
Applicant first came to the attention
of law enforcement on January 17, 2008,
when Louisiana State Police received a
call from a pharmacist that he had
authorized prescriptions for ‘‘excessive
amounts of name brand narcotics with
no generic substitutions allowed.’’ DI
Aff., at 2. Upon receipt of this
information, an undercover state trooper
(UC1) visited Applicant’s clinic with
audio/video recording equipment on
January 23, 2008. Id. When Applicant
asked UC1 ‘‘why he was there,’’ UC1
responded by requesting
‘‘[h]ydrocodone pain pills.’’ Id. UC1
‘‘initially denied that he was in pain
but, after negotiating with [Applicant],
PO 00000
Frm 00076
Fmt 4703
Sfmt 4703
he agreed to falsely state that he was
suffering from a sexually transmitted
disease,’’ and Applicant recorded this
false information in UC1’s medical file.
Id. Then, Applicant, without any
physical examination to verify the claim
of illness or symptoms, wrote
prescriptions for 15 Lortab 1 pills and an
antibiotic. Id. The undercover agent
paid $100 for the visit. Id.
Five days later, on January 28, 2008,
UC1 returned to Applicant’s clinic
seeking additional ‘‘pain pills.’’ Id.
However, Applicant denied his request
for more pain pills ‘‘because ‘big
brother’ was watching him.’’ Id.
Thereafter, on January 30, February 8,
and February 28, 2008, a second state
trooper (UC2) visited Applicant’s clinic
in an undercover capacity, while
equipped with an audio/video recording
device. Id. At UC2’s first visit,
Applicant issued her a prescription for
hydrocodone,2 notwithstanding UC2’s
‘‘initially den[ying] she was in pain’’
and ‘‘later stat[ing] she was in pain in
order to obtain a prescription for
hydrocodone.’’ Id. At her second visit
on February 8, Applicant provided
prescriptions for hydrocodone and
Phenergan with codeine,3 the latter
being a cough syrup, ‘‘even though she
had no cough or congestion and
exhibited no such symptoms.’’ Id. On
UC2’s third visit, she requested and
obtained from Applicant, prescriptions
for hydrocodone and Xanax.4 Id. To
justify issuing the prescriptions,
Applicant ‘‘coached’’ UC2 about what to
say and recorded the coached
statements in her medical file. Id. At the
undercover visits, Applicant never
‘‘require[d] any medical records nor did
he conduct any physical examinations.’’
Id.
On March 20, 2008, after a state court
judge issued a warrant for Applicant’s
arrest, Louisiana State Police alerted
DEA to the investigation and pending
arrest. Id. Thereafter, on March 26,
2008, Applicant was arrested and
charged with ‘‘six counts of prescribing
beyond authority and accepted medical
treatment, a violation of Louisiana
Revised Statute 40:971C(1).’’ Id. at 3.
Based on Applicant’s arrest, a DEA
Diversion Investigator asked for the
voluntary surrender of his DEA
1 Lortab, which is a combination drug containing
hydrocodone and acetaminophen, is a schedule III
controlled substance. 21 CFR 1308.13(e)(iv).
2 Hydrocodone is typically combined with
acetaminophen. In this formulation, it is a schedule
III controlled substance. 21 CFR 1308.13(e)(iv).
3 Phenergan with codeine cough syrup consists of
a combination of promethazine and codeine; it is
a schedule V controlled substance. 21 CFR
1308.15(c).
4 Xanax (alprazolam) is a schedule IV controlled
substance; 21 CFR 1308.14(c)(1).
E:\FR\FM\10AUN1.SGM
10AUN1
Federal Register / Vol. 76, No. 154 / Wednesday, August 10, 2011 / Notices
registration; Applicant agreed and
signed a DEA–104, Voluntary Surrender
of Controlled Substance Privileges. Id.
Four months later, on July 28, 2008,
Applicant submitted a DEA application
for a new registration as a practitioner
in schedules IV and V. Zavaleta
Application Information at 1. On his
application, Applicant stated that ‘‘the
medical board says there is no merit for
any disciplinary action,’’ he ‘‘can
continue working,’’ and his ‘‘license is
clear.’’ Id. Applicant further stated that
the State Police had yet to charge him
and that the charges may be dropped.
Id.
Discussion
Section 303(f) of the Controlled
Substances Act (CSA) provides that an
application for a practitioner’s
registration may be denied upon a
determination ‘‘that the issuance of such
registration would be inconsistent with
the public interest.’’ 21 U.S.C. 823(f). In
making the public interest
determination in the case of a
practitioner, Congress directed that the
following factors be considered:
emcdonald on DSK2BSOYB1PROD with NOTICES
(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.
‘‘[T]hese factors are considered in the
disjunctive.’’ Robert A. Leslie, 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
* * * to deny an application. 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) (citing Morall v. DEA, 412 F.3d
165, 173–74 (DC Cir. 2005)).
In this matter, while I have
considered all of the factors, I conclude
that it is not necessary to make findings
with respect to factors one (the
recommendation of the state licensing
board), three (applicant’s conviction
record) and five (such other conduct
which may threaten public health and
safety). I find that the Government’s
evidence with respect to Applicant’s
experience in dispensing controlled
substances (factor two) and his
compliance with applicable Federal and
VerDate Mar<15>2010
17:48 Aug 09, 2011
Jkt 223001
State laws related to the distribution
and dispensing of controlled substances
(factor four) makes out a prima facie
case that Applicant has committed acts
which render his registration
‘‘inconsistent with the public interest.’’
21 U.S.C. 823(f), 824(a)(4). I will
therefore order that his pending
application for registration be denied.
Factors Two and Four—Applicant’s
Experience in Dispensing Controlled
Substances and Compliance with
Applicable Laws Related to Controlled
Substances
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 related to controlled
substances.’’ Id.; see also La. Rev. Stat.
Ann. § 40:961(33) (2008) (effective Aug.
15, 2004); 5 La. Rev. Stat. Ann.
§ 40:1238.2(A) (2008) (effective Aug. 15,
2006).6
As the Supreme Court recently
explained, ‘‘the [CSA’s] 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, 143 (1975)); see also
5 Louisiana law defines the term ‘‘prescription’’ to
mean ‘‘a written request for a drug * * * issued by
a licensed physician * * * for a legitimate medical
purpose, for the purpose of correcting a physical,
mental, or bodily ailment, and acting in good faith
in the usual course of his professional practice.’’ La.
Rev. Stat. Ann. § 40.961(33).
6 This statute provides that:
A prescription, in order to be effective in
legalizing the possession of legend drugs, shall be
issued for a legitimate medical purpose by one
authorized to prescribe the use of such legend
drugs. An order purporting to be a prescription
issued to a drug abuser or habitual user of legend
drugs, not in the course of professional treatment,
is not a prescription within the meaning and intent
of this Section. Any person who knows or should
know that he or she is filling such a prescription
or order to a drug abuser or habitual user of legend
drugs, as well as the person issuing the
prescription, may be charged with a violation of
this Section.
La. Rev. Stat. Ann. § 40:1238.2(A).
PO 00000
Frm 00077
Fmt 4703
Sfmt 4703
49507
La. Rev. Stat. Ann. § 40:1238.2(A) (2008)
(effective Aug. 15, 2006).
Under the CSA, it is fundamental that
a practitioner must establish and
maintain 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.’’ Laurence
T. McKinney, 73 FR 43260, 43265 n.22
(2008); see also Moore, 423 U.S. at 142–
43 (noting that evidence established that
physician ‘‘exceeded the bounds of
‘professional practice,’ ’’ when ‘‘he gave
inadequate physical examinations or
none at all,’’ ‘‘ignored the results of the
tests he did make,’’ and ‘‘took no
precautions against * * * misuse and
diversion’’). The CSA 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); but see
21 U.S.C. 829(e)(2)(B) (providing
Federal standard for prescribing over
the Internet).
Under the regulation of the Louisiana
Board of Medical Examiners, in the
treatment of ‘‘intractable pain * * * a
physician shall comply’’ with the
Louisiana Pain Rules, including the
requirements that a physician perform
an ‘‘[e]valuation of the [p]atient’’ and
make a ‘‘[m]edical [d]iagnosis.’’ La.
Admin. Code tit. 46:XLV.6921(A)
(2008). ‘‘Evaluation of the patient shall
initially include relevant medical, pain,
alcohol and substance abuse histories,
an assessment of the impact of pain on
the patient’s physical and psychological
functions, a review of previous
diagnostics studies, previously utilized
therapies, an assessment of coexisting
illnesses, diseases, or conditions, and an
appropriate physical examination.’’ Id.
(emphasis added); see also Armstrong v.
La. State Bd. of Med. Examiners, 868 So.
2d 830, 840 (La.App. 4 Cir. Feb. 18,
2004) (upholding two year suspension
of physician’s license; noting that when
prescribing controlled substances for
relief of non-malignant pain is ’’
unaccompanied by appropriate testing,
diagnosis, oversight and monitoring
* * * the physician falls below
generally accepted standards of care’’);
Pastorek v. La. State Bd. of Med.
Examiners, 4 So. 3d 833 (La.App. 4 Cir.
Dec. 17, 2008). The Board’s rules further
require a ‘‘medical diagnosis * * * be
established and fully documented in the
patient’s medical record.’’ La. Admin.
Code tit. 46:XLV.6921(A)(2) (2008).
Louisiana law further prohibits a
physician from ‘‘[a]ssist[ing] a patient or
any other person in obtaining a
controlled dangerous substance through
E:\FR\FM\10AUN1.SGM
10AUN1
emcdonald on DSK2BSOYB1PROD with NOTICES
49508
Federal Register / Vol. 76, No. 154 / Wednesday, August 10, 2011 / Notices
misrepresentation, fraud, forgery,
deception, or subterfuge.’’ La. Rev. Stat.
Ann. § 40:971.2 (2008) (effective Aug.
15, 2005). It is also unlawful for a
physician to ‘‘prescribe * * * legally
controlled substances beyond his
respective prescribing authority or for a
purpose other than accepted medical
treatment of disease, condition, or
illness. Id., at § 40:971(C)(1) (2008)
(effective Sept. 9, 1988).
As found above, on four occasions,
Applicant prescribed drugs containing
hydrocodone (including Lortab and/or
Lorcet), which are schedule III
narcotics; Xanax, a schedule IV
controlled substance; and Phenergan
with codeine, a schedule V narcotic
cough syrup, to Louisiana State
Troopers acting in undercover
capacities. See DI Aff., at 2. Notably,
Applicant issued these prescriptions
without conducting a physical
examination at any of the visits and the
undercover agents received these
prescriptions even though they did not
demonstrate the conditions or
symptoms that would justify the
prescriptions. Id.
Moreover, both undercover agents
initially denied they were in pain, but
Applicant assisted the agents in
obtaining controlled substances by
encouraging them to make false
statements. See id. For example, while
he denied being in pain, UC1 asked
Applicant for ‘‘[h]ydrocodone pain
pills,’’ and then ‘‘negotiate[ed]’’ with
Applicant to ‘‘falsely state’’ he had a
sexually transmitted disease. Id.
Likewise, Applicant also ‘‘coached’’ the
second undercover agent on what to say
to ‘‘justify issuing the prescriptions and
wrote her coached statements in a
medical file.’’ Id. Therefore, I conclude
that Applicant failed to establish a
physician-patient relationship, lacked a
legitimate medical purpose, and acted
outside of the usual course of
professional practice in prescribing
controlled substances to the undercover
agents and thus violated Federal law.
See 21 CFR 1306.04(a); 21 U.S.C.
841(a)(1); see also Louisiana v. Moody,
393 So. 2d 1212, 1215 (La. 1981)
(holding that physician furnished
prescriptions for ‘‘other than a
legitimate medical purpose’’ based on
evidence showing that prescriptions
were issued in response to specific
requests of patients and physician did
not conduct physical examinations or
take medical histories).
I therefore hold that granting
Applicant’s application for a new
registration ‘‘would be inconsistent with
the public interest.’’ 21 U.S.C. 823(f).
Accordingly, I will order that
VerDate Mar<15>2010
17:48 Aug 09, 2011
Jkt 223001
Applicant’s pending application be
denied.
Order
[Notice 11–073]
Pursuant to the authority vested in me
by 21 U.S.C. 823(f) and 28 CFR 0.100(b),
I order that the application of Jose
Gonzalo Zavaleta, M.D., for a DEA
Certificate of Registration as a
practitioner be, and it hereby is, denied.
This order is effective September 9,
2011.
Dated: July 27, 2011.
Michele M. Leonhart,
Administrator.
[FR Doc. 2011–20284 Filed 8–9–11; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF LABOR
Office of Disability Employment
Program
‘‘Add Us In’’ Initiative
AGENCY: Office of Disability
Employment Policy, Department of
Labor.
ACTION: Correction to the Funding
Opportunity Number and Closing Date.
SUMMARY: The Office of Disability
Employment Policy, Department of
Labor is correcting the New Notice of
Availability of Funds and Solicitation
for Grant Applications (SGA) for
Cooperative Agreements published in
the Federal Register on August 4, 2011
at 76 FR 150. Specifically, we are
correcting the Funding Opportunity
Number to SGA 11–05 and the Closing
Date for receipt of applications to
September 2, 2011. The full Solicitation
for Grant Applications is posted on
https://www.grants.gov under U.S.
Department of Labor/ODEP. If you need
to speak to a person concerning these
grants, you may telephone Cassandra
Mitchell at 202–693–4570 (not a tollfree number).
Signed in Washington, DC, this 4th day of
August 2011.
Cassandra R. Mitchell,
Grant Officer.
[FR Doc. 2011–20211 Filed 8–9–11; 8:45 am]
BILLING CODE 4510–FT–P
PO 00000
NATIONAL AERONAUTICS AND
SPACE ADMINISTRATION
NASA Advisory Council; Science
Committee; Earth Science
Subcommittee; Meeting
AGENCY: National Aeronautics and
Space Administration.
ACTION:
Notice of meeting.
SUMMARY: In accordance with the
Federal Advisory Committee Act, Public
Law 92–463, as amended, the National
Aeronautics and Space Administration
(NASA) announces a meeting of the
Earth Science Subcommittee of the
NASA Advisory Council (NAC). This
Subcommittee reports to the Science
Committee of the NAC. The Meeting
will be held for the purpose of soliciting
from the scientific community and other
persons scientific and technical
information relevant to program
planning.
DATES: Wednesday, August 31, 1 p.m. to
3 p.m. E.D.T.
ADDRESSES: This meeting will take place
telephonically. Any interested person
may call the USA toll free conference
call number 888–603–9610, pass code
ESS, to participate in this meeting by
telephone.
FOR FURTHER INFORMATION CONTACT: Ms.
Marian Norris, Science Mission
Directorate, NASA Headquarters,
Washington, DC 20546, (202) 358–4452,
fax (202) 358–4118, or
mnorris@nasa.gov.
The
meeting will be open to the public up
to the capacity of the room. The agenda
for the meeting includes the following
topics:
SUPPLEMENTARY INFORMATION:
—Government Performance and Results
Act Review
It is imperative that the meeting be
held on these dates to accommodate the
scheduling priorities of the key
participants.
August 5, 2011.
Susan M. Burch,
Acting Director, Advisory Committee
Management Division, National Aeronautics
and Space Administration.
[FR Doc. 2011–20275 Filed 8–9–11; 8:45 am]
BILLING CODE 7510–13–P
Frm 00078
Fmt 4703
Sfmt 9990
E:\FR\FM\10AUN1.SGM
10AUN1
Agencies
[Federal Register Volume 76, Number 154 (Wednesday, August 10, 2011)]
[Notices]
[Pages 49506-49508]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-20284]
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Jose Gonzalo Zavaleta, M.D.; Denial of Application
On February 23, 2009, the Deputy Assistant Administrator, Office of
Diversion Control, Drug Enforcement Administration, issued an Order to
Show Cause (Order) to Jose Gonzalo Zavaleta, M.D. (Applicant), of
Pineville, Louisiana. The Order proposed the denial of Applicant's
pending application for a DEA Certificate of Registration as a
practitioner, on the ground that his registration would be
``inconsistent with the public interest.'' Order at 1 (citing 21 U.S.C.
823(f)).
The Order alleged that Applicant voluntarily surrendered his DEA
Certificate of Registration, BZ5998250, on March 26, 2008, after being
charged with six counts of prescribing controlled substances beyond
authority and accepted medical treatment, in violation of La. Rev.
Stat. Ann. Sec. 40:971 (C)(1)(2008) (effective Aug. 15, 2006). Id. The
Order further alleged that Applicant prescribed controlled substances
to undercover agents with ``cursory or no medical examinations, and
without a legitimate medical purpose in violation of 21 U.S.C.
841(a)(1).'' Id. More specifically, the Order alleged that Applicant
prescribed a total of 75 dosage units of hydrocodone (including Lortab
and/or Lorcet), which are schedule III narcotics; 20 dosage units of
Xanax, a schedule IV controlled substance; and six ounces of Phenergan
with codeine, a schedule V narcotic cough syrup. Id. Finally, the Order
that alleged ``[Applicant] facilitated the undercover officers'
procurement of drugs by fraudulent means'' when he advised them to
``provide false medical information'' to justify ``illegitimate
prescriptions.'' Id. at 2.
On March 2, 2009, the Order, which also notified Applicant of his
right to either request a hearing on the allegations or to submit a
written statement in lieu of a hearing, the procedures for doing so,
and the consequence if he failed to do so, was served on Applicant by
certified mail addressed to him at the address listed on his
application. Id. at 2 (citing 21 CFR 1316.47; 21 CFR 1301.43). Since
service of the Order, more than thirty days have now passed and neither
Applicant, nor anyone purporting to represent him, has either requested
a hearing or submitted a written statement in lieu of a hearing. See 21
CFR 1301.43(b)-(d). Accordingly, I find that Applicant has waived his
rights to a hearing or to submit a written statement. Id. 1301.43(d). I
therefore issue this Decision and Final Order without a hearing based
on relevant material contained in the investigative record submitted by
the Government. I make the following findings.
Findings
Applicant was previously the holder of DEA Certificate of
Registration, BZ5998250, which authorized him to dispense controlled
substances in schedules II through V as a practitioner at the
registered location of 5629 Jackson Street Ext, Alexandria, Louisiana.
Affidavit of Diversion Investigator (hereinafter, DI Aff.), at 1;
Applicant Registration Information, at 1. However, on March 26, 2008,
concurrent with Applicant's arrest on state drug charges (the
circumstances of which are set forth below), he voluntarily surrendered
his registration. DI Aff., at 1. Applicant's registration was then
retired by DEA on March 27, 2008. Applicant Registration Information,
at 1. On July 28, 2008, Applicant applied for a new DEA registration as
a practitioner in schedules IV and V. Id.
Applicant first came to the attention of law enforcement on January
17, 2008, when Louisiana State Police received a call from a pharmacist
that he had authorized prescriptions for ``excessive amounts of name
brand narcotics with no generic substitutions allowed.'' DI Aff., at 2.
Upon receipt of this information, an undercover state trooper (UC1)
visited Applicant's clinic with audio/video recording equipment on
January 23, 2008. Id. When Applicant asked UC1 ``why he was there,''
UC1 responded by requesting ``[h]ydrocodone pain pills.'' Id. UC1
``initially denied that he was in pain but, after negotiating with
[Applicant], he agreed to falsely state that he was suffering from a
sexually transmitted disease,'' and Applicant recorded this false
information in UC1's medical file. Id. Then, Applicant, without any
physical examination to verify the claim of illness or symptoms, wrote
prescriptions for 15 Lortab \1\ pills and an antibiotic. Id. The
undercover agent paid $100 for the visit. Id.
---------------------------------------------------------------------------
\1\ Lortab, which is a combination drug containing hydrocodone
and acetaminophen, is a schedule III controlled substance. 21 CFR
1308.13(e)(iv).
---------------------------------------------------------------------------
Five days later, on January 28, 2008, UC1 returned to Applicant's
clinic seeking additional ``pain pills.'' Id. However, Applicant denied
his request for more pain pills ``because `big brother' was watching
him.'' Id.
Thereafter, on January 30, February 8, and February 28, 2008, a
second state trooper (UC2) visited Applicant's clinic in an undercover
capacity, while equipped with an audio/video recording device. Id. At
UC2's first visit, Applicant issued her a prescription for
hydrocodone,\2\ notwithstanding UC2's ``initially den[ying] she was in
pain'' and ``later stat[ing] she was in pain in order to obtain a
prescription for hydrocodone.'' Id. At her second visit on February 8,
Applicant provided prescriptions for hydrocodone and Phenergan with
codeine,\3\ the latter being a cough syrup, ``even though she had no
cough or congestion and exhibited no such symptoms.'' Id. On UC2's
third visit, she requested and obtained from Applicant, prescriptions
for hydrocodone and Xanax.\4\ Id. To justify issuing the prescriptions,
Applicant ``coached'' UC2 about what to say and recorded the coached
statements in her medical file. Id. At the undercover visits, Applicant
never ``require[d] any medical records nor did he conduct any physical
examinations.'' Id.
---------------------------------------------------------------------------
\2\ Hydrocodone is typically combined with acetaminophen. In
this formulation, it is a schedule III controlled substance. 21 CFR
1308.13(e)(iv).
\3\ Phenergan with codeine cough syrup consists of a combination
of promethazine and codeine; it is a schedule V controlled
substance. 21 CFR 1308.15(c).
\4\ Xanax (alprazolam) is a schedule IV controlled substance; 21
CFR 1308.14(c)(1).
---------------------------------------------------------------------------
On March 20, 2008, after a state court judge issued a warrant for
Applicant's arrest, Louisiana State Police alerted DEA to the
investigation and pending arrest. Id. Thereafter, on March 26, 2008,
Applicant was arrested and charged with ``six counts of prescribing
beyond authority and accepted medical treatment, a violation of
Louisiana Revised Statute 40:971C(1).'' Id. at 3. Based on Applicant's
arrest, a DEA Diversion Investigator asked for the voluntary surrender
of his DEA
[[Page 49507]]
registration; Applicant agreed and signed a DEA-104, Voluntary
Surrender of Controlled Substance Privileges. Id.
Four months later, on July 28, 2008, Applicant submitted a DEA
application for a new registration as a practitioner in schedules IV
and V. Zavaleta Application Information at 1. On his application,
Applicant stated that ``the medical board says there is no merit for
any disciplinary action,'' he ``can continue working,'' and his
``license is clear.'' Id. Applicant further stated that the State
Police had yet to charge him and that the charges may be dropped. Id.
Discussion
Section 303(f) of the Controlled Substances Act (CSA) provides that
an application for a practitioner's registration may be denied upon a
determination ``that the issuance of such registration would be
inconsistent with the public interest.'' 21 U.S.C. 823(f). In making
the public interest determination in the case of a practitioner,
Congress directed that the following factors be considered:
(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.
``[T]hese factors are considered in the disjunctive.'' Robert A.
Leslie, 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 * * * to deny an application. 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) (citing
Morall v. DEA, 412 F.3d 165, 173-74 (DC Cir. 2005)).
In this matter, while I have considered all of the factors, I
conclude that it is not necessary to make findings with respect to
factors one (the recommendation of the state licensing board), three
(applicant's conviction record) and five (such other conduct which may
threaten public health and safety). I find that the Government's
evidence with respect to Applicant's experience in dispensing
controlled substances (factor two) and his compliance with applicable
Federal and State laws related to the distribution and dispensing of
controlled substances (factor four) makes out a prima facie case that
Applicant has committed acts which render his registration
``inconsistent with the public interest.'' 21 U.S.C. 823(f), 824(a)(4).
I will therefore order that his pending application for registration be
denied.
Factors Two and Four--Applicant's Experience in Dispensing Controlled
Substances and Compliance with Applicable Laws Related to Controlled
Substances
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 related to controlled
substances.'' Id.; see also La. Rev. Stat. Ann. Sec. 40:961(33) (2008)
(effective Aug. 15, 2004); \5\ La. Rev. Stat. Ann. Sec. 40:1238.2(A)
(2008) (effective Aug. 15, 2006).\6\
---------------------------------------------------------------------------
\5\ Louisiana law defines the term ``prescription'' to mean ``a
written request for a drug * * * issued by a licensed physician * *
* for a legitimate medical purpose, for the purpose of correcting a
physical, mental, or bodily ailment, and acting in good faith in the
usual course of his professional practice.'' La. Rev. Stat. Ann.
Sec. 40.961(33).
\6\ This statute provides that:
A prescription, in order to be effective in legalizing the
possession of legend drugs, shall be issued for a legitimate medical
purpose by one authorized to prescribe the use of such legend drugs.
An order purporting to be a prescription issued to a drug abuser or
habitual user of legend drugs, not in the course of professional
treatment, is not a prescription within the meaning and intent of
this Section. Any person who knows or should know that he or she is
filling such a prescription or order to a drug abuser or habitual
user of legend drugs, as well as the person issuing the
prescription, may be charged with a violation of this Section.
La. Rev. Stat. Ann. Sec. 40:1238.2(A).
---------------------------------------------------------------------------
As the Supreme Court recently explained, ``the [CSA's] 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, 143 (1975)); see also La. Rev. Stat. Ann. Sec. 40:1238.2(A)
(2008) (effective Aug. 15, 2006).
Under the CSA, it is fundamental that a practitioner must establish
and maintain 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.'' Laurence T.
McKinney, 73 FR 43260, 43265 n.22 (2008); see also Moore, 423 U.S. at
142-43 (noting that evidence established that physician ``exceeded the
bounds of `professional practice,' '' when ``he gave inadequate
physical examinations or none at all,'' ``ignored the results of the
tests he did make,'' and ``took no precautions against * * * misuse and
diversion''). The CSA 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); but see
21 U.S.C. 829(e)(2)(B) (providing Federal standard for prescribing over
the Internet).
Under the regulation of the Louisiana Board of Medical Examiners,
in the treatment of ``intractable pain * * * a physician shall comply''
with the Louisiana Pain Rules, including the requirements that a
physician perform an ``[e]valuation of the [p]atient'' and make a
``[m]edical [d]iagnosis.'' La. Admin. Code tit. 46:XLV.6921(A) (2008).
``Evaluation of the patient shall initially include relevant medical,
pain, alcohol and substance abuse histories, an assessment of the
impact of pain on the patient's physical and psychological functions, a
review of previous diagnostics studies, previously utilized therapies,
an assessment of coexisting illnesses, diseases, or conditions, and an
appropriate physical examination.'' Id. (emphasis added); see also
Armstrong v. La. State Bd. of Med. Examiners, 868 So. 2d 830, 840
(La.App. 4 Cir. Feb. 18, 2004) (upholding two year suspension of
physician's license; noting that when prescribing controlled substances
for relief of non-malignant pain is '' unaccompanied by appropriate
testing, diagnosis, oversight and monitoring * * * the physician falls
below generally accepted standards of care''); Pastorek v. La. State
Bd. of Med. Examiners, 4 So. 3d 833 (La.App. 4 Cir. Dec. 17, 2008). The
Board's rules further require a ``medical diagnosis * * * be
established and fully documented in the patient's medical record.'' La.
Admin. Code tit. 46:XLV.6921(A)(2) (2008).
Louisiana law further prohibits a physician from ``[a]ssist[ing] a
patient or any other person in obtaining a controlled dangerous
substance through
[[Page 49508]]
misrepresentation, fraud, forgery, deception, or subterfuge.'' La. Rev.
Stat. Ann. Sec. 40:971.2 (2008) (effective Aug. 15, 2005). It is also
unlawful for a physician to ``prescribe * * * legally controlled
substances beyond his respective prescribing authority or for a purpose
other than accepted medical treatment of disease, condition, or
illness. Id., at Sec. 40:971(C)(1) (2008) (effective Sept. 9, 1988).
As found above, on four occasions, Applicant prescribed drugs
containing hydrocodone (including Lortab and/or Lorcet), which are
schedule III narcotics; Xanax, a schedule IV controlled substance; and
Phenergan with codeine, a schedule V narcotic cough syrup, to Louisiana
State Troopers acting in undercover capacities. See DI Aff., at 2.
Notably, Applicant issued these prescriptions without conducting a
physical examination at any of the visits and the undercover agents
received these prescriptions even though they did not demonstrate the
conditions or symptoms that would justify the prescriptions. Id.
Moreover, both undercover agents initially denied they were in
pain, but Applicant assisted the agents in obtaining controlled
substances by encouraging them to make false statements. See id. For
example, while he denied being in pain, UC1 asked Applicant for
``[h]ydrocodone pain pills,'' and then ``negotiate[ed]'' with Applicant
to ``falsely state'' he had a sexually transmitted disease. Id.
Likewise, Applicant also ``coached'' the second undercover agent on
what to say to ``justify issuing the prescriptions and wrote her
coached statements in a medical file.'' Id. Therefore, I conclude that
Applicant failed to establish a physician-patient relationship, lacked
a legitimate medical purpose, and acted outside of the usual course of
professional practice in prescribing controlled substances to the
undercover agents and thus violated Federal law. See 21 CFR 1306.04(a);
21 U.S.C. 841(a)(1); see also Louisiana v. Moody, 393 So. 2d 1212, 1215
(La. 1981) (holding that physician furnished prescriptions for ``other
than a legitimate medical purpose'' based on evidence showing that
prescriptions were issued in response to specific requests of patients
and physician did not conduct physical examinations or take medical
histories).
I therefore hold that granting Applicant's application for a new
registration ``would be inconsistent with the public interest.'' 21
U.S.C. 823(f). Accordingly, I will order that Applicant's pending
application be denied.
Order
Pursuant to the authority vested in me by 21 U.S.C. 823(f) and 28
CFR 0.100(b), I order that the application of Jose Gonzalo Zavaleta,
M.D., for a DEA Certificate of Registration as a practitioner be, and
it hereby is, denied. This order is effective September 9, 2011.
Dated: July 27, 2011.
Michele M. Leonhart,
Administrator.
[FR Doc. 2011-20284 Filed 8-9-11; 8:45 am]
BILLING CODE 4410-09-P