Vaccine Information Statements for Influenza Vaccines; Revised Instructions for Use of Vaccine Information Statements, 68461-68465 [05-22441]
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Federal Register / Vol. 70, No. 217 / Thursday, November 10, 2005 / Notices
Dated: November 4, 2005.
Betsey S. Dunaway,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. 05–22440 Filed 11–9–05; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Vaccine Information Statements for
Influenza Vaccines; Revised
Instructions for Use of Vaccine
Information Statements
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice.
AGENCY:
SUMMARY: Under the National
Childhood Vaccine Injury Act (NCVIA)
(42 U.S.C. 300aa-26), the CDC must
develop vaccine information materials
that all health care providers are
required to give to patients/parents prior
to administration of specific vaccines.
On July 28, 2005, CDC published a
notice in the Federal Register (70 FR
43694) seeking public comments on
proposed new vaccine information
materials for trivalent influenza
vaccines and hepatitis A vaccines. The
60 day comment period ended on
September 26, 2005. Following review
of the comments submitted and
consultation as required under the law,
CDC has finalized the influenza vaccine
information materials. The final
influenza materials, and revised
instructions for their use and for use of
materials for other covered vaccines, are
contained in this notice. The final
hepatitis A vaccine information
materials will be published later.
DATES: Beginning no later than January
1, 2006, each health care provider who
administers any trivalent influenza
vaccine to any child or adult in the
United States shall provide copies of the
relevant vaccine information materials
contained in this notice, dated October
20, 2005, in conformance with the
November 4, 2005 CDC Instructions for
the Use of Vaccine Information
Statements, also contained in this
notice.
FOR FURTHER INFORMATION CONTACT:
Stephen L. Cochi, M.D., M.P.H., Acting
Director, National Immunization
Program, Centers for Disease Control
and Prevention, Mailstop E–05, 1600
Clifton Road, NE., Atlanta, Georgia
30333, telephone (404) 639–8200.
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The
National Childhood Vaccine Injury Act
of 1986 (Pub. L. 99–660), as amended by
section 708 of Public Law 103–183,
added section 2126 to the Public Health
Service Act. Section 2126, codified at 42
U.S.C. 300aa–26, requires the Secretary
of Health and Human Services to
develop and disseminate vaccine
information materials for distribution by
all health care providers in the United
States to any patient (or to the parent or
legal representative in the case of a
child) receiving vaccines covered under
the National Vaccine Injury
Compensation Program.
Development and revision of the
vaccine information materials, also
known as Vaccine Information
Statements (VIS), have been delegated
by the Secretary to the Centers for
Disease Control and Prevention (CDC).
Section 2126 requires that the materials
be developed, or revised, after notice to
the public, with a 60-day comment
period, and in consultation with the
Advisory Commission on Childhood
Vaccines, appropriate health care
provider and parent organizations, and
the Food and Drug Administration. The
law also requires that the information
contained in the materials be based on
available data and information, be
presented in understandable terms, and
include:
(1) A concise description of the
benefits of the vaccine,
(2) A concise description of the risks
associated with the vaccine,
(3) A statement of the availability of
the National Vaccine Injury
Compensation Program, and
(4) Such other relevant information as
may be determined by the Secretary.
The vaccines initially covered under
the National Vaccine Injury
Compensation Program were diphtheria,
tetanus, pertussis, measles, mumps,
rubella and poliomyelitis vaccines.
Since April 15, 1992, any health care
provider in the United States who
intends to administer one of these
covered vaccines is required to provide
copies of the relevant vaccine
information materials prior to
administration of any of these vaccines.
Since June 1, 1999, health care
providers are also required to provide
copies of vaccine information materials
for the following vaccines that were
added to the National Vaccine Injury
Compensation Program: hepatitis B,
haemophilus influenzae type b (Hib),
and varicella (chickenpox) vaccines. In
addition, use of vaccine information
materials for pneumococcal conjugate
vaccine has been required since
December 15, 2002.
SUPPLEMENTARY INFORMATION:
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Instructions for use of the vaccine
information materials and copies of the
materials can be downloaded in PDF
format from the CDC Web site at: https://
www.cdc.gov/nip/publications/VIS. In
addition, single camera-ready copies are
available from State health departments.
A list of State health department
contacts for obtaining copies of these
materials is included in a December 17,
1999 Federal Register notice (64 FR
70914).
New Vaccine Information Materials
Inactivated Influenza Vaccine
Information Statement; Live, Intranasal
Influenza Vaccine Information
Statement; Hepatitis A Vaccine
Information Statement
Following the addition of hepatitis A
and trivalent influenza vaccines to the
National Vaccine Injury Compensation
Program, CDC, as required under 42
U.S.C. 300aa–26, proposed vaccine
information materials covering those
vaccines in a Federal Register notice
published on July 28, 2005 (70 FR
43694). In order to have Influenza
Vaccine Information Statements
available for voluntary use in the
current influenza vaccination season,
the proposed influenza vaccine
materials were also issued as interim
VISs through that notice.
The new vaccine information
materials referenced in this notice were
developed in consultation with the
Advisory Commission on Childhood
Vaccines, the Food and Drug
Administration, the American Academy
of Family Physicians, American
Academy of Pediatrics, American
Medical Association, Emory Vaccine
Research Center, Every Child By Two,
Immunization Action Coalition and the
National PTA. Also, CDC sought
consultation with other organizations;
however, those organizations did not
provide comments.
Following consultation and review of
comments submitted, the vaccine
information materials covering trivalent
influenza vaccines have been finalized
and are contained in this notice. These
Vaccine Information Statements, dated
October 20, 2005, are entitled:
‘‘Inactivated Influenza Vaccine: What
You Need to Know’’ and ‘‘Live,
Intranasal Influenza Vaccine: What You
Need to Know.’’ CDC has also revised
the ‘‘Instructions for the Use of Vaccine
Information Statements.’’ The vaccine
information materials covering hepatitis
A vaccine will be finalized and
published at a later date.
With publication of this notice, as of
January 1, 2006, all health care
providers will be required to provide
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Federal Register / Vol. 70, No. 217 / Thursday, November 10, 2005 / Notices
copies of influenza vaccine information
materials prior to immunization in
conformance with CDC’s November 4,
2005 ‘‘Instructions for the Use of
Vaccine Information Statements’’ which
are contained in this notice.
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Instructions for the Use of Vaccine
Information Statements
Required Use
1. Provide Vaccine Information
Statement (VIS) When Vaccination Is
Given
As required under the National
Childhood Vaccine Injury Act (42 U.S.C.
300aa–26), all health care providers in
the United States who administer to any
child or adult any vaccine containing
diphtheria, tetanus, pertussis, measles,
mumps, rubella, polio, Haemophilus
influenzae type b (Hib), hepatitis B,
trivalent influenza (use of influenza
VISs required effective January 1, 2006),
pneumococcal conjugate, or varicella
(chickenpox) vaccine shall, prior to
administration of each dose of the
vaccine, provide a copy to keep of the
relevant current edition vaccine
information materials that have been
produced by the Centers for Disease
Control and Prevention (CDC):
• To the parent or legal
representative* of any child to whom
the provider intends to administer such
vaccine, and
• To any adult to whom the provider
intends to administer such vaccine. (In
the case of an incompetent adult,
relevant VISs shall be provided to the
individual’s legal representative.* If the
incompetent adult is living in a longterm care facility, all relevant VISs may
be provided at the time of admission, or
at the time of consent if later than
admission, rather than prior to each
immunization.)
The materials shall be supplemented
with visual presentations or oral
explanations, as appropriate.
If there is not a single VIS for a
combination vaccine, use the VISs for
all component vaccines.
• A Legal representative is defined as
a parent or other individual who is
qualified under State law to consent to
the immunization of a minor child or
incompetent adult.
2. Record information for each VIS
provided
Health care providers shall make a
notation in each patient’s permanent
medical record at the time vaccine
information materials are provided
indicating (1) the edition date of the
Vaccine Information Statement
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distributed and (2) the date the VIS was
provided.
This recordkeeping requirement
supplements the requirement of 42
U.S.C. 300aa–25 that all health care
providers administering these vaccines
must record in the patient’s permanent
medical record (or in a permanent office
log): (3) The name, address and title of
the individual who administers the
vaccine, (4) the date of administration
and (5) the vaccine manufacturer and lot
number of the vaccine used.
Applicability of State Law
Health care providers should consult
their legal counsel to determine
additional State requirements pertaining
to immunization. The Federal
requirement to provide the vaccine
information materials supplements any
applicable State laws.
Availability of Copies
Single camera-ready copies of the
vaccine information materials are
available from State health departments.
Copies are also available on the Centers
for Disease Control and Prevention’s
Web site at https://www.cdc.gov/nip/
publications/VIS. Copies are available
in English and in other languages.
Edition Dates of Current VISs
Diphtheria, Tetanus, Pertussis (DTaP/
DT): July 30, 2001.
Haemophilus influenzae type b (Hib):
December 16, 1998.
Hepatitis B: July 11, 2001.
Inactivated Influenza: October 20,
2005.
Live, Intranasal Influenza: October 20,
2005.
Measles, Mumps, Rubella (MMR):
January 15, 2003.
Pneumococcal conjugate: September
30, 2002.
Polio: January 1, 2000.
Tetanus Diphtheria (Td): June 10,
1994.
Varicella (chickenpox): December 16,
1998.
Reference 42 U.S.C. 300aa–26: November 4,
2005.
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Inactivated Influenza Vaccine
Information Statement
Inactivated Influenza Vaccine: What
You Need To Know
1. Why get vaccinated?
Influenza (‘‘flu’’) is a very contagious
disease.
It is caused by the influenza virus,
which spreads from infected persons to
the nose or throat of others.
Other illnesses can have the same
symptoms and are often mistaken for
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influenza. But only an illness caused by
the influenza virus is really influenza.
Anyone can get influenza. For most
people, it lasts only a few days. It can
cause:
• Fever • Sore throat • Chills
• Fatigue • Cough • Headache
• Muscle aches.
Some people get much sicker.
Influenza can lead to pneumonia and
can be dangerous for people with heart
or breathing conditions. It can cause
high fever and seizures in children.
Influenza kills about 36,000 people each
year in the United States, mostly among
the elderly.
Influenza vaccine can prevent
influenza.
2. Inactivated influenza vaccine.
There are two types of influenza
vaccine:
An inactivated (killed) vaccine, given
as a shot, has been used in the United
States for many years.
A live, weakened vaccine was
licensed in 2003. It is sprayed into the
nostrils. This vaccine is described in a
separate Vaccine Information Statement.
Influenza viruses are constantly
changing. Therefore, influenza vaccines
are updated every year, and an annual
vaccination is recommended.
For most people influenza vaccine
prevents serious illness caused by the
influenza virus. It will not prevent
‘‘influenza-like’’ illnesses caused by
other viruses.
It takes about 2 weeks for protection
to develop after the shot, and protection
can last up to a year.
Inactivated influenza vaccine may be
given at the same time as other vaccines,
including pneumococcal vaccine.
Some inactivated influenza vaccine
contains thimerosal, a preservative that
contains mercury. Some people believe
thimerosal may be related to
developmental problems in children. In
2004 the Institute of Medicine
published a report concluding that,
based on scientific studies, there is no
evidence of such a relationship. If you
are concerned about thimerosal, ask
your doctor about thimerosal-free
influenza vaccine.
3. Who should get inactivated influenza
vaccine?
Influenza vaccine can be given to
people 6 months of age and older. It is
recommended for people who are at risk
of serious influenza or its
complications, and for people who can
spread influenza to those at high risk
(including all household members):
People at high risk for complications
from influenza:
• All children 6–23 months of age.
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• People 65 years of age and older.
• Residents of long-term care
facilities housing persons with chronic
medical conditions.
• People who have long-term health
problems with:
—Heart disease
—Lung disease
—Asthma
—Kidney disease
—Metabolic disease, such as diabetes
—Anemia, and other blood disorders
• People with certain muscle or nerve
disorders (such as seizure disorders or
severe cerebral palsy) that can lead to
breathing or swallowing problems.
• People with a weakened immune
system due to:
—HIV/AIDS or other diseases affecting
the immune system.
—Long-term treatment with drugs such
as steroids.
—Cancer treatment with x-rays or drugs.
• People 6 months to 18 years of age
on long-term aspirin treatment (these
people could develop Reye Syndrome if
they got influenza).
• Women who will be pregnant
during influenza season.
People who can spread influenza to
those at high risk:
• Household contacts and out-ofhome caretakers of infants from 0–23
months of age.
• Physicians, nurses, family
members, or anyone else in close
contact with people at risk of serious
influenza.
Influenza vaccine is also
recommended for adults 50–64 years of
age and anyone else who wants to
reduce their chance of catching
influenza.
An annual flu shot should be
considered for:
• People who provide essential
community services.
• People living in dormitories or
under other crowded conditions, to
prevent outbreaks.
• People at high risk of influenza
complications who travel to the
Southern hemisphere between April
and September, or to the tropics or in
organized tourist groups at any time.
4. When should I get influenza vaccine?
The best time to get influenza vaccine
is in October or November.
Influenza season usually peaks in
February, but it can peak any time from
November through May. So getting the
vaccine in December, or even later, can
be beneficial in most years.
Some people should get their flu shot
in October or earlier:
—People 50 years of age and older,
—Younger people at high risk from
influenza and its complications
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(including children 6 through 23
months of age),
—Household contacts of people at high
risk,
—Healthcare workers, and
—Children younger than 9 years of age
getting influenza vaccine for the first
time.
Most people need one flu shot each
year. Children younger than 9 years of
age getting influenza vaccine for the first
time should get 2 doses, given at least
one month apart.
occur, it is within a few minutes to a
few hours after the shot.
• In 1976, a certain type of influenza
(swine flu) vaccine was associated with
´
Guillain-Barre Syndrome (GBS). Since
then, flu vaccines have not been clearly
linked to GBS. However, if there is a
risk of GBS from current flu vaccines, it
would be no more than 1 or 2 cases per
million people vaccinated. This is much
lower than the risk of severe influenza,
which can be prevented by vaccination.
5. Some people should talk with a
doctor before getting influenza vaccine.
What should I look for?
• Any unusual condition, such as a
high fever or behavior changes. Signs of
a serious allergic reaction can include
difficulty breathing, hoarseness or
wheezing, hives, paleness, weakness, a
fast heart beat or dizziness.
What should I do?
• Call a doctor, or get the person to
a doctor right away.
• Tell your doctor what happened,
the date and time it happened, and
when the vaccination was given.
• Ask your doctor, nurse, or health
department to report the reaction by
filing a Vaccine Adverse Event
Reporting System (VAERS) form.
Or you can file this report through the
VAERS Web site at https://
www.vaers.hhs.gov, or by calling 1–800–
822–7967. VAERS does not provide
medical advice.
Some people should not get
inactivated influenza vaccine or should
wait before getting it.
• Tell your doctor if you have any
severe (life-threatening) allergies.
Allergic reactions to influenza vaccine
are rare.
—Influenza vaccine virus is grown in
eggs. People with a severe egg allergy
should not get the vaccine.
—A severe allergy to any vaccine
component is also a reason to not get
the vaccine.
—If you have had a severe reaction after
a previous dose of influenza vaccine,
tell your doctor.
• Tell your doctor if you ever had
´
Guillain-Barre Syndrome (a severe
paralytic illness, also called GBS). You
may be able to get the vaccine, but your
doctor should help you make the
decision.
• People who are moderately or
severely ill should usually wait until
they recover before getting flu vaccine.
If you are ill, talk to your doctor or
nurse about whether to reschedule the
vaccination. People with a mild illness
can usually get the vaccine.
6. What are the risks from inactivated
influenza vaccine?
A vaccine, like any medicine, could
possibly cause serious problems, such
as severe allergic reactions. The risk of
a vaccine causing serious harm, or
death, is extremely small.
Serious problems from influenza
vaccine are very rare. The viruses in
inactivated influenza vaccine have been
killed, so you cannot get influenza from
the vaccine.
Mild problems:
• Soreness, redness, or swelling
where the shot was given.
• Fever.
• Aches.
If these problems occur, they usually
begin soon after the shot and last 1–2
days.
Severe problems:
• Life-threatening allergic reactions
from vaccines are very rare. If they do
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7. What if there is a severe reaction?
8. The National Vaccine Injury
Compensation Program
In the event that you or your child has
a serious reaction to a vaccine, a federal
program has been created to help pay
for the care of those who have been
harmed.
For details about the National Vaccine
Injury Compensation Program, call 1–
800–338–2382 or visit their Web site at
https://www.hrsa.gov/osp/vicp.
9. How can I learn more?
• Ask your immunization provider.
They can give you the vaccine package
insert or suggest other sources of
information.
• Call your local or state health
department.
• Contact the Centers for Disease
Control and Prevention (CDC):
—Call 1–800–232–4636 (1–800–CDC–
INFO)
—Visit CDC’s Web site at https://
www.cdc.gov/flu.
—Vaccine Information Statement.
—(October 20, 2005) Inactivated
Influenza Vaccine.
42 U.S.C. 300aa–26.
Department of Health and Human
Services, Centers for Disease Control
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and Prevention, National Immunization
Program.
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Live, Intranasal Influenza Vaccine
Information Statement
Live Intranasal Influenza Vaccine: What
You Need to Know
1. Why get vaccinated?
Influenza (‘‘flu’’) is a very contagious
disease.
It is caused by the influenza virus,
which spreads from infected persons to
the nose or throat of others.
Other illnesses can have the same
symptoms and are often mistaken for
influenza. But only an illness caused by
the influenza virus is really influenza.
Anyone can get influenza, but rates of
infection are highest among children.
For most people, it lasts only a few
days. It can cause:
• Fever
• Sore throat
• Chills
• Fatigue
• Cough
• Headache
• Muscle aches
Some people get much sicker.
Influenza can lead to pneumonia and
can be dangerous for people with heart
or breathing conditions. It can cause
high fever and seizures in children.
Influenza kills about 36,000 people each
year in the United States.
Influenza vaccine can prevent
influenza.
2. Live, attenuated influenza vaccine
(nasal spray)
There are two types of influenza
vaccine:
Live, attenuated influenza vaccine
(LAIV) was licensed in 2003. LAIV
contains live but attenuated (weakened)
influenza virus. It is sprayed into the
nostrils rather than injected into the
muscle. It is recommended for healthy
children and adults from 5 through 49
years of age, who are not pregnant.
Inactivated influenza vaccine,
sometimes called the ‘‘flu shot,’’ has
been used for many years and is given
by injection. This vaccine is described
in a separate Vaccine Information
Statement.
Influenza viruses are constantly
changing. Therefore, influenza vaccines
are updated every year, and annual
vaccination is recommended.
For most people influenza vaccine
prevents serious illness caused by the
influenza virus. It will not prevent
‘‘influenza-like’’ illnesses caused by
other viruses.
It takes about 2 weeks for protection
to develop after vaccination, and
protection can last up to a year.
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3. Who can get LAIV?
Live, intranasal influenza vaccine is
approved for healthy children and
adults from 5 through 49 years of age,
including those who can spread
influenza to people at high risk, such as:
• Household contacts and out-ofhome caretakers of infants from 0–23
months of age.
• Physicians and nurses, and family
members or anyone else in close contact
with people at risk of serious influenza.
Influenza vaccine is also
recommended for anyone else who
wants to reduce their chance of catching
influenza.
LAIV may be considered for:
• People who provide essential
community services.
• People living in dormitories or
under other crowded conditions, to
prevent outbreaks.
4. Who should not get LAIV?
LAIV is not licensed for everyone.
The following people should check with
their health-care provider about getting
the inactivated vaccine:
• Adults 50 years of age or older or
children younger than 5.
• People who have long-term health
problems with:
—Heart disease
—Lung disease
—Asthma
—Kidney disease
—Metabolic disease, such as diabetes
—Anemia, and other blood disorders
• People with a weakened immune
system.
• Children or adolescents on longterm aspirin treatment.
• Pregnant women.
• Anyone with a history of Guillain´
Barre syndrome (a severe paralytic
illness, also called GBS).
Inactivated influenza vaccine (the flu
shot) is the preferred vaccine for people
(including health-care workers and
family members) coming in close
contact with anyone who has a severely
weakened immune system (that is,
anyone who requires care in a protected
environment).
Some people should talk with a
doctor before getting either influenza
vaccine:
• Anyone who has ever had a serious
allergic reaction to eggs or to a previous
dose of influenza vaccine.
• People who are moderately or
severely ill should usually wait until
they recover before getting flu vaccine.
If you are ill, talk to your doctor or
nurse about whether to reschedule the
vaccination. People with a mild illness
can usually get the vaccine.
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5. When should I get influenza vaccine?
The best time to get influenza vaccine
is in October or November, but LAIV
may be given as soon as it is available.
Influenza season usually peaks in
February, but it can peak any time from
November through May. So getting the
vaccine in December, or even later, can
be beneficial in most years.
Most people need one dose of
influenza vaccine each year. Children
younger than 9 years of age getting
influenza vaccine for the first time
should get 2 doses For LAIV, these
doses should be given 6–10 weeks apart.
LAIV may be given at the same time
as other vaccines.
6. What are the risks from LAIV?
A vaccine, like any medicine, could
possibly cause serious problems, such
as severe allergic reactions. However,
the risk of a vaccine causing serious
harm, or death, is extremely small.
Live influenza vaccine viruses rarely
spread from person to person. Even if
they do, they are not likely to cause
illness.
LAIV is made from weakened virus
and does not cause influenza. The
vaccine can cause mild symptoms in
people who get it (see below).
Mild problems:
Some children and adolescents 5–17
years of age have reported mild
reactions, including:
• Runny nose, nasal congestion or
cough.
• Headache and muscle aches.
• Fever.
• Abdominal pain or occasional
vomiting or diarrhea.
Some adults 18–49 years of age have
reported:
• Runny nose or nasal congestion.
• Sore throat.
• Cough, chills, tiredness/weakness.
• Headache.
These symptoms did not last long and
went away on their own. Although they
can occur after vaccination, they may
not have been caused by the vaccine.
Severe problems:
• Life-threatening allergic reactions
from vaccines are very rare. If they do
occur, it is within a few minutes to a
few hours after the vaccination.
• If rare reactions occur with any new
product, they may not be identified
until thousands, or millions, of people
have used it. Over two million doses of
LAIV have been distributed since it was
licensed, and no serious problems have
been identified. Like all vaccines, LAIV
will continue to be monitored for
unusual or severe problems.
7. What if there is a severe reaction?
What should I look for?
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• Any unusual condition, such as a
high fever or behavior changes. Signs of
a serious allergic reaction can include
difficulty breathing, hoarseness or
wheezing, hives, paleness, weakness, a
fast heart beat or dizziness.
What should I do?
• Call a doctor, or get the person to
a doctor right away.
• Tell your doctor what happened,
the date and time it happened, and
when the vaccination was given.
• Ask your doctor, nurse, or health
department to report the reaction by
filing a Vaccine Adverse Event
Reporting System (VAERS) form.
Or you can file this report through the
VAERS Web site at https://
www.vaers.hhs.gov, or by calling 1–800–
822–7967.
VAERS does not provide medical
advice.
8. The National Vaccine Injury
Compensation Program
In the event that you or your child has
a serious reaction to a vaccine, a Federal
program has been created to help pay
for the care of those who have been
harmed.
For details about the National Vaccine
Injury Compensation Program, call 1–
800–338–2382 or visit their Web site at
https://www.hrsa.gov/osp/vicp.
9. How can I learn more?
• Ask your immunization provider.
They can give you the vaccine package
insert or suggest other sources of
information.
• Call your local or state health
department.
• Contact the Centers for Disease
Control and Prevention (CDC):
—Call 1–800–232–4636 (1–800–CDC–
INFO).
—Visit CDC’s Web site at https://
www.cdc.gov/flu.
—Vaccine Information Statement.
—Live, Attenuated Influenza Vaccine.
(October 20, 2005)
42 U.S.C. 300aa–26.
Department of Health and Human Services,
Centers for Disease Control and Prevention,
National Immunization Program.
Dated: November 4, 2005.
James D. Seligman,
Associate Director for Program Services,
Centers for Disease Control and Prevention.
[FR Doc. 05–22441 Filed 11–9–05; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. 2001D–0281]
Medical Devices: A Pilot Program to
Evaluate a Proposed Globally
Harmonized Alternative for Premarket
Procedures; Guidance for Industry and
FDA Staff; Availability
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing the
availability of a guidance entitled ‘‘A
Pilot Program to Evaluate a Proposed
Globally Harmonized Alternative for
Premarket Procedures; Guidance for
Industry and FDA Staff.’’ The revised
guidance extends the voluntary pilot
premarket review program Summary
Technical Documentation (STED pilot)
until we have received an adequate
number of submissions to evaluate the
STED pilot. The pilot program is
intended for evaluating the utility of an
alternative submission procedure.
DATES: Submit written or electronic
comments on the guidance at any time.
Submit written requests for
single copies on a 3.5’’ diskette of the
guidance document entitled ‘‘A Pilot
Program to Evaluate a Proposed
Globally Harmonized Alternative for
Premarket Procedures; Guidance for
Industry and FDA Staff’’ to the Division
of Small Manufacturers, International,
and Consumer Assistance (HFZ–220),
Center for Devices and Radiological
Health, Food and Drug Administration,
1350 Piccard Dr., Rockville, MD 20850.
Send one self-addressed adhesive label
to assist that office in processing your
request, or fax your request to 301–443–
8818. See SUPPLEMENTARY INFORMATION
section for information on electronic
access to the guidance.
Submit written comments concerning
this guidance to the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852. Submit
electronic comments to https://
www.fda.gov/dockets/ecomments.
Identify comments with the docket
number found in brackets in the
heading of this document.
FOR FURTHER INFORMATION CONTACT:
Harry R. Sauberman, Center for Devices
and Radiological Health (HFZ–480),
Food and Drug Administration, 9200
Corporate Blvd., Rockville, MD 20850,
301–443–4879, or Kenneth J. Cavanaugh
Jr., Center for Devices and Radiological
ADDRESSES:
PO 00000
Frm 00074
Fmt 4703
Sfmt 4703
68465
Health (HFZ–450), Food and Drug
Administration, 9200 Corporate Blvd.,
Rockville, MD 20850, 301–443–8517.
SUPPLEMENTARY INFORMATION:
I. Background
In the Federal Register of June 26,
2003 (68 FR 38068), FDA announced the
availability of a guidance document
entitled ‘‘A Pilot Program to Evaluate a
Proposed Globally Harmonized
Alternative for Premarket Procedures;
Guidance for Industry and FDA Staff.’’
The guidance document announced a
pilot program for a premarket review
program and encouraged participation
from the medical device industry. The
pilot program is intended to evaluate
the utility of an alternative submission
procedure as described in the draft
STED document prepared by Study
Group 1 of the Global Harmonization
Task Force (GHTF). The document seeks
to harmonize the different requirements
for premarket submissions in various
countries.
The June 26, 2003, guidance and
notice of availability announced that the
pilot program would be in effect for 1
year from the date of publication of the
notice of availability. In the Federal
Register of July 23, 2004 (69 FR 44040),
the pilot program was subsequently
extended until June 25, 2005. FDA has
received no comments on the guidance
issued on June 26, 2003, or the updated
version published on July 23, 2004. In
this revised guidance, FDA is extending
the pilot program until we have
received a sufficient number of
submissions to evaluate the pilot
program. In addition, FDA is updating
the contact information and the
references to the GHTF documents,
along with other minor editorial
changes. The FDA guidance document
is intended to assist the medical device
industry in making submissions to FDA
that use a proposed internationally
harmonized format and content for
premarket submissions, e.g., premarket
approval applications and 510(k)
submissions in the United States. The
revised guidance is a level 2 guidance
under FDA’s good guidance practices
(GGPs) regulation (21 CFR 10.115). FDA
made the guidance available on its Web
site at https://www.fda.gov/cdrh/ode/
guidance/1347.html.
The GHTF is a voluntary group
comprised of medical device regulatory
officials and industry representatives
from the United States, Canada,
Australia, the European Union, and
Japan. The goals of the GHTF include
the following items: (1) Encourage
convergence in regulatory practices with
respect to ensuring the safety,
effectiveness, performance, and quality
E:\FR\FM\10NON1.SGM
10NON1
Agencies
[Federal Register Volume 70, Number 217 (Thursday, November 10, 2005)]
[Notices]
[Pages 68461-68465]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-22441]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
Vaccine Information Statements for Influenza Vaccines; Revised
Instructions for Use of Vaccine Information Statements
AGENCY: Centers for Disease Control and Prevention (CDC), Department of
Health and Human Services (HHS).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: Under the National Childhood Vaccine Injury Act (NCVIA) (42
U.S.C. 300aa-26), the CDC must develop vaccine information materials
that all health care providers are required to give to patients/parents
prior to administration of specific vaccines. On July 28, 2005, CDC
published a notice in the Federal Register (70 FR 43694) seeking public
comments on proposed new vaccine information materials for trivalent
influenza vaccines and hepatitis A vaccines. The 60 day comment period
ended on September 26, 2005. Following review of the comments submitted
and consultation as required under the law, CDC has finalized the
influenza vaccine information materials. The final influenza materials,
and revised instructions for their use and for use of materials for
other covered vaccines, are contained in this notice. The final
hepatitis A vaccine information materials will be published later.
DATES: Beginning no later than January 1, 2006, each health care
provider who administers any trivalent influenza vaccine to any child
or adult in the United States shall provide copies of the relevant
vaccine information materials contained in this notice, dated October
20, 2005, in conformance with the November 4, 2005 CDC Instructions for
the Use of Vaccine Information Statements, also contained in this
notice.
FOR FURTHER INFORMATION CONTACT: Stephen L. Cochi, M.D., M.P.H., Acting
Director, National Immunization Program, Centers for Disease Control
and Prevention, Mailstop E-05, 1600 Clifton Road, NE., Atlanta, Georgia
30333, telephone (404) 639-8200.
SUPPLEMENTARY INFORMATION: The National Childhood Vaccine Injury Act of
1986 (Pub. L. 99-660), as amended by section 708 of Public Law 103-183,
added section 2126 to the Public Health Service Act. Section 2126,
codified at 42 U.S.C. 300aa-26, requires the Secretary of Health and
Human Services to develop and disseminate vaccine information materials
for distribution by all health care providers in the United States to
any patient (or to the parent or legal representative in the case of a
child) receiving vaccines covered under the National Vaccine Injury
Compensation Program.
Development and revision of the vaccine information materials, also
known as Vaccine Information Statements (VIS), have been delegated by
the Secretary to the Centers for Disease Control and Prevention (CDC).
Section 2126 requires that the materials be developed, or revised,
after notice to the public, with a 60-day comment period, and in
consultation with the Advisory Commission on Childhood Vaccines,
appropriate health care provider and parent organizations, and the Food
and Drug Administration. The law also requires that the information
contained in the materials be based on available data and information,
be presented in understandable terms, and include:
(1) A concise description of the benefits of the vaccine,
(2) A concise description of the risks associated with the vaccine,
(3) A statement of the availability of the National Vaccine Injury
Compensation Program, and
(4) Such other relevant information as may be determined by the
Secretary.
The vaccines initially covered under the National Vaccine Injury
Compensation Program were diphtheria, tetanus, pertussis, measles,
mumps, rubella and poliomyelitis vaccines. Since April 15, 1992, any
health care provider in the United States who intends to administer one
of these covered vaccines is required to provide copies of the relevant
vaccine information materials prior to administration of any of these
vaccines. Since June 1, 1999, health care providers are also required
to provide copies of vaccine information materials for the following
vaccines that were added to the National Vaccine Injury Compensation
Program: hepatitis B, haemophilus influenzae type b (Hib), and
varicella (chickenpox) vaccines. In addition, use of vaccine
information materials for pneumococcal conjugate vaccine has been
required since December 15, 2002.
Instructions for use of the vaccine information materials and
copies of the materials can be downloaded in PDF format from the CDC
Web site at: https://www.cdc.gov/nip/publications/VIS. In addition,
single camera-ready copies are available from State health departments.
A list of State health department contacts for obtaining copies of
these materials is included in a December 17, 1999 Federal Register
notice (64 FR 70914).
New Vaccine Information Materials
Inactivated Influenza Vaccine Information Statement; Live, Intranasal
Influenza Vaccine Information Statement; Hepatitis A Vaccine
Information Statement
Following the addition of hepatitis A and trivalent influenza
vaccines to the National Vaccine Injury Compensation Program, CDC, as
required under 42 U.S.C. 300aa-26, proposed vaccine information
materials covering those vaccines in a Federal Register notice
published on July 28, 2005 (70 FR 43694). In order to have Influenza
Vaccine Information Statements available for voluntary use in the
current influenza vaccination season, the proposed influenza vaccine
materials were also issued as interim VISs through that notice.
The new vaccine information materials referenced in this notice
were developed in consultation with the Advisory Commission on
Childhood Vaccines, the Food and Drug Administration, the American
Academy of Family Physicians, American Academy of Pediatrics, American
Medical Association, Emory Vaccine Research Center, Every Child By Two,
Immunization Action Coalition and the National PTA. Also, CDC sought
consultation with other organizations; however, those organizations did
not provide comments.
Following consultation and review of comments submitted, the
vaccine information materials covering trivalent influenza vaccines
have been finalized and are contained in this notice. These Vaccine
Information Statements, dated October 20, 2005, are entitled:
``Inactivated Influenza Vaccine: What You Need to Know'' and ``Live,
Intranasal Influenza Vaccine: What You Need to Know.'' CDC has also
revised the ``Instructions for the Use of Vaccine Information
Statements.'' The vaccine information materials covering hepatitis A
vaccine will be finalized and published at a later date.
With publication of this notice, as of January 1, 2006, all health
care providers will be required to provide
[[Page 68462]]
copies of influenza vaccine information materials prior to immunization
in conformance with CDC's November 4, 2005 ``Instructions for the Use
of Vaccine Information Statements'' which are contained in this notice.
* * * * *
Instructions for the Use of Vaccine Information Statements
Required Use
1. Provide Vaccine Information Statement (VIS) When Vaccination Is
Given
As required under the National Childhood Vaccine Injury Act (42
U.S.C. 300aa-26), all health care providers in the United States who
administer to any child or adult any vaccine containing diphtheria,
tetanus, pertussis, measles, mumps, rubella, polio, Haemophilus
influenzae type b (Hib), hepatitis B, trivalent influenza (use of
influenza VISs required effective January 1, 2006), pneumococcal
conjugate, or varicella (chickenpox) vaccine shall, prior to
administration of each dose of the vaccine, provide a copy to keep of
the relevant current edition vaccine information materials that have
been produced by the Centers for Disease Control and Prevention (CDC):
To the parent or legal representative* of any child to
whom the provider intends to administer such vaccine, and
To any adult to whom the provider intends to administer
such vaccine. (In the case of an incompetent adult, relevant VISs shall
be provided to the individual's legal representative.* If the
incompetent adult is living in a long-term care facility, all relevant
VISs may be provided at the time of admission, or at the time of
consent if later than admission, rather than prior to each
immunization.)
The materials shall be supplemented with visual presentations or
oral explanations, as appropriate.
If there is not a single VIS for a combination vaccine, use the
VISs for all component vaccines.
A Legal representative is defined as a parent or other
individual who is qualified under State law to consent to the
immunization of a minor child or incompetent adult.
2. Record information for each VIS provided
Health care providers shall make a notation in each patient's
permanent medical record at the time vaccine information materials are
provided indicating (1) the edition date of the Vaccine Information
Statement distributed and (2) the date the VIS was provided.
This recordkeeping requirement supplements the requirement of 42
U.S.C. 300aa-25 that all health care providers administering these
vaccines must record in the patient's permanent medical record (or in a
permanent office log): (3) The name, address and title of the
individual who administers the vaccine, (4) the date of administration
and (5) the vaccine manufacturer and lot number of the vaccine used.
Applicability of State Law
Health care providers should consult their legal counsel to
determine additional State requirements pertaining to immunization. The
Federal requirement to provide the vaccine information materials
supplements any applicable State laws.
Availability of Copies
Single camera-ready copies of the vaccine information materials are
available from State health departments. Copies are also available on
the Centers for Disease Control and Prevention's Web site at https://
www.cdc.gov/nip/publications/VIS. Copies are available in English and
in other languages.
Edition Dates of Current VISs
Diphtheria, Tetanus, Pertussis (DTaP/DT): July 30, 2001.
Haemophilus influenzae type b (Hib): December 16, 1998.
Hepatitis B: July 11, 2001.
Inactivated Influenza: October 20, 2005.
Live, Intranasal Influenza: October 20, 2005.
Measles, Mumps, Rubella (MMR): January 15, 2003.
Pneumococcal conjugate: September 30, 2002.
Polio: January 1, 2000.
Tetanus Diphtheria (Td): June 10, 1994.
Varicella (chickenpox): December 16, 1998.
Reference 42 U.S.C. 300aa-26: November 4, 2005.
* * * * *
Inactivated Influenza Vaccine Information Statement
Inactivated Influenza Vaccine: What You Need To Know
1. Why get vaccinated?
Influenza (``flu'') is a very contagious disease.
It is caused by the influenza virus, which spreads from infected
persons to the nose or throat of others.
Other illnesses can have the same symptoms and are often mistaken
for influenza. But only an illness caused by the influenza virus is
really influenza.
Anyone can get influenza. For most people, it lasts only a few
days. It can cause:
Fever Sore throat Chills
Fatigue Cough Headache Muscle aches.
Some people get much sicker. Influenza can lead to pneumonia and
can be dangerous for people with heart or breathing conditions. It can
cause high fever and seizures in children. Influenza kills about 36,000
people each year in the United States, mostly among the elderly.
Influenza vaccine can prevent influenza.
2. Inactivated influenza vaccine.
There are two types of influenza vaccine:
An inactivated (killed) vaccine, given as a shot, has been used in
the United States for many years.
A live, weakened vaccine was licensed in 2003. It is sprayed into
the nostrils. This vaccine is described in a separate Vaccine
Information Statement.
Influenza viruses are constantly changing. Therefore, influenza
vaccines are updated every year, and an annual vaccination is
recommended.
For most people influenza vaccine prevents serious illness caused
by the influenza virus. It will not prevent ``influenza-like''
illnesses caused by other viruses.
It takes about 2 weeks for protection to develop after the shot,
and protection can last up to a year.
Inactivated influenza vaccine may be given at the same time as
other vaccines, including pneumococcal vaccine.
Some inactivated influenza vaccine contains thimerosal, a
preservative that contains mercury. Some people believe thimerosal may
be related to developmental problems in children. In 2004 the Institute
of Medicine published a report concluding that, based on scientific
studies, there is no evidence of such a relationship. If you are
concerned about thimerosal, ask your doctor about thimerosal-free
influenza vaccine.
3. Who should get inactivated influenza vaccine?
Influenza vaccine can be given to people 6 months of age and older.
It is recommended for people who are at risk of serious influenza or
its complications, and for people who can spread influenza to those at
high risk (including all household members):
People at high risk for complications from influenza:
All children 6-23 months of age.
[[Page 68463]]
People 65 years of age and older.
Residents of long-term care facilities housing persons
with chronic medical conditions.
People who have long-term health problems with:
--Heart disease
--Lung disease
--Asthma
--Kidney disease
--Metabolic disease, such as diabetes
--Anemia, and other blood disorders
People with certain muscle or nerve disorders (such as
seizure disorders or severe cerebral palsy) that can lead to breathing
or swallowing problems.
People with a weakened immune system due to:
--HIV/AIDS or other diseases affecting the immune system.
--Long-term treatment with drugs such as steroids.
--Cancer treatment with x-rays or drugs.
People 6 months to 18 years of age on long-term aspirin
treatment (these people could develop Reye Syndrome if they got
influenza).
Women who will be pregnant during influenza season.
People who can spread influenza to those at high risk:
Household contacts and out-of-home caretakers of infants
from 0-23 months of age.
Physicians, nurses, family members, or anyone else in
close contact with people at risk of serious influenza.
Influenza vaccine is also recommended for adults 50-64 years of age
and anyone else who wants to reduce their chance of catching influenza.
An annual flu shot should be considered for:
People who provide essential community services.
People living in dormitories or under other crowded
conditions, to prevent outbreaks.
People at high risk of influenza complications who travel
to the Southern hemisphere between April and September, or to the
tropics or in organized tourist groups at any time.
4. When should I get influenza vaccine?
The best time to get influenza vaccine is in October or November.
Influenza season usually peaks in February, but it can peak any
time from November through May. So getting the vaccine in December, or
even later, can be beneficial in most years.
Some people should get their flu shot in October or earlier:
--People 50 years of age and older,
--Younger people at high risk from influenza and its complications
(including children 6 through 23 months of age),
--Household contacts of people at high risk,
--Healthcare workers, and
--Children younger than 9 years of age getting influenza vaccine for
the first time.
Most people need one flu shot each year. Children younger than 9
years of age getting influenza vaccine for the first time should get 2
doses, given at least one month apart.
5. Some people should talk with a doctor before getting influenza
vaccine.
Some people should not get inactivated influenza vaccine or should
wait before getting it.
Tell your doctor if you have any severe (life-threatening)
allergies. Allergic reactions to influenza vaccine are rare.
--Influenza vaccine virus is grown in eggs. People with a severe egg
allergy should not get the vaccine.
--A severe allergy to any vaccine component is also a reason to not get
the vaccine.
--If you have had a severe reaction after a previous dose of influenza
vaccine, tell your doctor.
Tell your doctor if you ever had Guillain-Barr[eacute]
Syndrome (a severe paralytic illness, also called GBS). You may be able
to get the vaccine, but your doctor should help you make the decision.
People who are moderately or severely ill should usually
wait until they recover before getting flu vaccine. If you are ill,
talk to your doctor or nurse about whether to reschedule the
vaccination. People with a mild illness can usually get the vaccine.
6. What are the risks from inactivated influenza vaccine?
A vaccine, like any medicine, could possibly cause serious
problems, such as severe allergic reactions. The risk of a vaccine
causing serious harm, or death, is extremely small.
Serious problems from influenza vaccine are very rare. The viruses
in inactivated influenza vaccine have been killed, so you cannot get
influenza from the vaccine.
Mild problems:
Soreness, redness, or swelling where the shot was given.
Fever.
Aches.
If these problems occur, they usually begin soon after the shot and
last 1-2 days.
Severe problems:
Life-threatening allergic reactions from vaccines are very
rare. If they do occur, it is within a few minutes to a few hours after
the shot.
In 1976, a certain type of influenza (swine flu) vaccine
was associated with Guillain-Barr[eacute] Syndrome (GBS). Since then,
flu vaccines have not been clearly linked to GBS. However, if there is
a risk of GBS from current flu vaccines, it would be no more than 1 or
2 cases per million people vaccinated. This is much lower than the risk
of severe influenza, which can be prevented by vaccination.
7. What if there is a severe reaction?
What should I look for?
Any unusual condition, such as a high fever or behavior
changes. Signs of a serious allergic reaction can include difficulty
breathing, hoarseness or wheezing, hives, paleness, weakness, a fast
heart beat or dizziness.
What should I do?
Call a doctor, or get the person to a doctor right away.
Tell your doctor what happened, the date and time it
happened, and when the vaccination was given.
Ask your doctor, nurse, or health department to report the
reaction by filing a Vaccine Adverse Event Reporting System (VAERS)
form.
Or you can file this report through the VAERS Web site at https://
www.vaers.hhs.gov, or by calling 1-800-822-7967. VAERS does not provide
medical advice.
8. The National Vaccine Injury Compensation Program
In the event that you or your child has a serious reaction to a
vaccine, a federal program has been created to help pay for the care of
those who have been harmed.
For details about the National Vaccine Injury Compensation Program,
call 1-800-338-2382 or visit their Web site at https://www.hrsa.gov/osp/
vicp.
9. How can I learn more?
Ask your immunization provider. They can give you the
vaccine package insert or suggest other sources of information.
Call your local or state health department.
Contact the Centers for Disease Control and Prevention
(CDC):
--Call 1-800-232-4636 (1-800-CDC-INFO)
--Visit CDC's Web site at https://www.cdc.gov/flu.
--Vaccine Information Statement.
--(October 20, 2005) Inactivated Influenza Vaccine.
42 U.S.C. 300aa-26.
Department of Health and Human Services, Centers for Disease
Control
[[Page 68464]]
and Prevention, National Immunization Program.
* * * * *
Live, Intranasal Influenza Vaccine Information Statement
Live Intranasal Influenza Vaccine: What You Need to Know
1. Why get vaccinated?
Influenza (``flu'') is a very contagious disease.
It is caused by the influenza virus, which spreads from infected
persons to the nose or throat of others.
Other illnesses can have the same symptoms and are often mistaken
for influenza. But only an illness caused by the influenza virus is
really influenza.
Anyone can get influenza, but rates of infection are highest among
children. For most people, it lasts only a few days. It can cause:
Fever
Sore throat
Chills
Fatigue
Cough
Headache
Muscle aches
Some people get much sicker. Influenza can lead to pneumonia and
can be dangerous for people with heart or breathing conditions. It can
cause high fever and seizures in children. Influenza kills about 36,000
people each year in the United States.
Influenza vaccine can prevent influenza.
2. Live, attenuated influenza vaccine (nasal spray)
There are two types of influenza vaccine:
Live, attenuated influenza vaccine (LAIV) was licensed in 2003.
LAIV contains live but attenuated (weakened) influenza virus. It is
sprayed into the nostrils rather than injected into the muscle. It is
recommended for healthy children and adults from 5 through 49 years of
age, who are not pregnant.
Inactivated influenza vaccine, sometimes called the ``flu shot,''
has been used for many years and is given by injection. This vaccine is
described in a separate Vaccine Information Statement.
Influenza viruses are constantly changing. Therefore, influenza
vaccines are updated every year, and annual vaccination is recommended.
For most people influenza vaccine prevents serious illness caused
by the influenza virus. It will not prevent ``influenza-like''
illnesses caused by other viruses.
It takes about 2 weeks for protection to develop after vaccination,
and protection can last up to a year.
3. Who can get LAIV?
Live, intranasal influenza vaccine is approved for healthy children
and adults from 5 through 49 years of age, including those who can
spread influenza to people at high risk, such as:
Household contacts and out-of-home caretakers of infants
from 0-23 months of age.
Physicians and nurses, and family members or anyone else
in close contact with people at risk of serious influenza.
Influenza vaccine is also recommended for anyone else who wants to
reduce their chance of catching influenza.
LAIV may be considered for:
People who provide essential community services.
People living in dormitories or under other crowded
conditions, to prevent outbreaks.
4. Who should not get LAIV?
LAIV is not licensed for everyone. The following people should
check with their health-care provider about getting the inactivated
vaccine:
Adults 50 years of age or older or children younger than
5.
People who have long-term health problems with:
--Heart disease
--Lung disease
--Asthma
--Kidney disease
--Metabolic disease, such as diabetes
--Anemia, and other blood disorders
People with a weakened immune system.
Children or adolescents on long-term aspirin treatment.
Pregnant women.
Anyone with a history of Guillain-Barr[eacute] syndrome (a
severe paralytic illness, also called GBS).
Inactivated influenza vaccine (the flu shot) is the preferred
vaccine for people (including health-care workers and family members)
coming in close contact with anyone who has a severely weakened immune
system (that is, anyone who requires care in a protected environment).
Some people should talk with a doctor before getting either
influenza vaccine:
Anyone who has ever had a serious allergic reaction to
eggs or to a previous dose of influenza vaccine.
People who are moderately or severely ill should usually
wait until they recover before getting flu vaccine. If you are ill,
talk to your doctor or nurse about whether to reschedule the
vaccination. People with a mild illness can usually get the vaccine.
5. When should I get influenza vaccine?
The best time to get influenza vaccine is in October or November,
but LAIV may be given as soon as it is available. Influenza season
usually peaks in February, but it can peak any time from November
through May. So getting the vaccine in December, or even later, can be
beneficial in most years.
Most people need one dose of influenza vaccine each year. Children
younger than 9 years of age getting influenza vaccine for the first
time should get 2 doses For LAIV, these doses should be given 6-10
weeks apart.
LAIV may be given at the same time as other vaccines.
6. What are the risks from LAIV?
A vaccine, like any medicine, could possibly cause serious
problems, such as severe allergic reactions. However, the risk of a
vaccine causing serious harm, or death, is extremely small.
Live influenza vaccine viruses rarely spread from person to person.
Even if they do, they are not likely to cause illness.
LAIV is made from weakened virus and does not cause influenza. The
vaccine can cause mild symptoms in people who get it (see below).
Mild problems:
Some children and adolescents 5-17 years of age have reported mild
reactions, including:
Runny nose, nasal congestion or cough.
Headache and muscle aches.
Fever.
Abdominal pain or occasional vomiting or diarrhea.
Some adults 18-49 years of age have reported:
Runny nose or nasal congestion.
Sore throat.
Cough, chills, tiredness/weakness.
Headache.
These symptoms did not last long and went away on their own.
Although they can occur after vaccination, they may not have been
caused by the vaccine.
Severe problems:
Life-threatening allergic reactions from vaccines are very
rare. If they do occur, it is within a few minutes to a few hours after
the vaccination.
If rare reactions occur with any new product, they may not
be identified until thousands, or millions, of people have used it.
Over two million doses of LAIV have been distributed since it was
licensed, and no serious problems have been identified. Like all
vaccines, LAIV will continue to be monitored for unusual or severe
problems.
7. What if there is a severe reaction?
What should I look for?
[[Page 68465]]
Any unusual condition, such as a high fever or behavior
changes. Signs of a serious allergic reaction can include difficulty
breathing, hoarseness or wheezing, hives, paleness, weakness, a fast
heart beat or dizziness.
What should I do?
Call a doctor, or get the person to a doctor right away.
Tell your doctor what happened, the date and time it
happened, and when the vaccination was given.
Ask your doctor, nurse, or health department to report the
reaction by filing a Vaccine Adverse Event Reporting System (VAERS)
form.
Or you can file this report through the VAERS Web site at https://
www.vaers.hhs.gov, or by calling 1-800-822-7967.
VAERS does not provide medical advice.
8. The National Vaccine Injury Compensation Program
In the event that you or your child has a serious reaction to a
vaccine, a Federal program has been created to help pay for the care of
those who have been harmed.
For details about the National Vaccine Injury Compensation Program,
call 1-800-338-2382 or visit their Web site at https://www.hrsa.gov/osp/
vicp.
9. How can I learn more?
Ask your immunization provider. They can give you the
vaccine package insert or suggest other sources of information.
Call your local or state health department.
Contact the Centers for Disease Control and Prevention
(CDC):
--Call 1-800-232-4636 (1-800-CDC-INFO).
--Visit CDC's Web site at https://www.cdc.gov/flu.
--Vaccine Information Statement.
--Live, Attenuated Influenza Vaccine.
(October 20, 2005)
42 U.S.C. 300aa-26.
Department of Health and Human Services, Centers for Disease
Control and Prevention, National Immunization Program.
Dated: November 4, 2005.
James D. Seligman,
Associate Director for Program Services, Centers for Disease Control
and Prevention.
[FR Doc. 05-22441 Filed 11-9-05; 8:45 am]
BILLING CODE 4163-18-P