[Federal Register Volume 75, Number 154 (Wednesday, August 11, 2010)]
[Notices]
[Pages 48706-48707]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2010-19782]



[[Page 48706]]

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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention


Proposed Vaccine Information Materials for Rotavirus Vaccine

AGENCY: Centers for Disease Control and Prevention (CDC), Department of 
Health and Human Services (HHS).

ACTION: Notice with comment period.

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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. CDC seeks written comment 
on proposed new vaccine information materials for rotavirus vaccine.

DATES: Written comments are invited and must be received on or before 
October 12, 2010.

ADDRESSES: Written comments should be addressed to Anne Schuchat, M.D., 
Director, National Center for Immunization and Respiratory Diseases, 
Centers for Disease Control and Prevention, Mailstop E-05, 1600 Clifton 
Road, NE., Atlanta, Georgia 30333.

FOR FURTHER INFORMATION CONTACT: Skip Wolfe, National Center for 
Immunization and Respiratory Diseases, Centers for Disease Control and 
Prevention, Mailstop E-52, 1600 Clifton Road, NE., Atlanta, Georgia 
30333, telephone (404) 639-8809.

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 then, the following vaccines have been added to the 
National Vaccine Injury Compensation Program, requiring use of vaccine 
information materials for them as well: hepatitis B, haemophilus 
influenzae type b (Hib), varicella (chickenpox), pneumococcal 
conjugate, rotavirus, hepatitis A, meningococcal, human papillomavirus 
(HPV), and trivalent influenza vaccines. Instructions for use of the 
vaccine information materials and copies of the materials can be found 
on the CDC Web site at: http://www.cdc.gov/vaccines/pubs/VIS/. In 
addition, single camera-ready copies may be 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).

Proposed Rotavirus Vaccine Information Materials

    With the publication in 2009 of updated Advisory Committee on 
Immunization Practices (ACIP) recommendations for rotavirus vaccine, 
incorporating information about both the pentavalent and newer 
monovalent formulations, CDC, as required under 42 U.S.C. 300aa-26, is 
proposing vaccine information materials covering rotavirus vaccine, 
which are included in this notice. Interim materials have been 
available for use pending completion of the formal development process.

Development of Vaccine Information Materials

    The vaccine information materials referenced in this notice are 
being developed in consultation with the Advisory Commission on 
Childhood Vaccines, the Food and Drug Administration, and parent and 
health care provider groups.
    In addition, we invite written comment on the proposed vaccine 
information materials that follow, entitled ``Rotavirus Vaccine: What 
You Need to Know.'' Comments submitted will be considered in finalizing 
these materials. When the final materials are published in the Federal 
Register, the notice will include an effective date for their mandatory 
use.
    We also propose to revise the June 9, 2010 Instructions for the Use 
of Vaccine Information Statements to update references to these vaccine 
information materials.
* * * * *
    Proposed Rotavirus Vaccine Information Statement:

Rotavirus Vaccine: What You Need To Know

1. What is rotavirus?

    Rotavirus is a virus that causes severe diarrhea, mostly in babies 
and young children. It is often accompanied by vomiting and fever. 
Rotavirus is not the only cause of severe diarrhea, but it is one of 
the most serious. Before rotavirus vaccine was used, rotavirus was 
responsible for:
     More than 400,000 doctor visits,
     More than 200,000 emergency room visits,
     55,000 to 70,000 hospitalizations, and
     20-60 deaths in the United States each year.
    Almost all children in the U.S. are infected with rotavirus before 
their 5th birthday.
    Children are most likely to get rotavirus diarrhea between November 
and May, depending on the part of the country.

2. Rotavirus Vaccine

    Better hygiene and sanitation have not reduced rotavirus diarrhea 
very much in the United States. The best way to protect your baby is 
with rotavirus vaccine.
    Rotavirus vaccine is an oral (swallowed) vaccine, not a shot.
    Rotavirus vaccine will not prevent diarrhea or vomiting caused by 
other germs, but it is very good at preventing diarrhea and vomiting 
caused by rotavirus. Most babies who get the vaccine will not get 
rotavirus diarrhea at

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all, and almost all of them will be protected from severe rotavirus 
diarrhea.
    Babies who get the vaccine are also much less likely to be 
hospitalized or to see a doctor because of rotavirus diarrhea.
    A virus (or parts of the virus) called porcine circovirus is in 
both rotavirus vaccines. This virus is not known to infect people and 
there is no known safety risk. For more information, see http://www.fda.gov, and search for ``porcine circovirus.''

3. Who should get rotavirus vaccine and when?

    There are two brands of rotavirus vaccine. A baby should get either 
2 or 3 doses, depending on which brand is used.
    The doses are recommended at these ages:

First Dose: 2 months of age
Second Dose: 4 months of age
Third Dose: 6 months of age (if needed)

    The first dose may be given as early as 6 weeks of age, and should 
be given by age 14 weeks 6 days. The last dose should be given by 8 
months of age.
    Rotavirus vaccine may be given at the same time as other childhood 
vaccines.

4. Some Babies Should Not Get Rotavirus Vaccine or Should Wait

     A baby who has had a severe (life-threatening) allergic 
reaction to a dose of rotavirus vaccine should not get another dose. A 
baby who has a severe (life threatening) allergy to any component of 
rotavirus vaccine should not get the vaccine. Tell your doctor if your 
baby has any severe allergies that you know of, including a severe 
allergy to latex.
     Babies with ``severe combined immunodeficiency'' (SCID) 
should not get rotavirus vaccine.
     Babies who are moderately or severely ill at the time the 
vaccination is scheduled should probably wait until they recover. This 
includes babies who have moderate or severe diarrhea or vomiting. Ask 
your doctor or nurse. Babies with mild illnesses should usually get the 
vaccine.
     Check with your doctor if your baby's immune system is 
weakened because of:

--HIV/AIDS, or any other disease that affects the immune system
--Treatment with drugs such as long-term steroids
--Cancer, or cancer treatment with x-rays or drugs

    In the late 1990s a different type of rotavirus vaccine was used. 
This vaccine was found to be associated with an uncommon type of bowel 
obstruction called ``intussusception,'' and it was taken off the 
market.
    The new rotavirus vaccines have not been associated with 
intussusception.
    However, babies who have had intussusception, from any cause, are 
at higher risk for getting it again. If your baby has ever had 
intussusception, discuss this with your doctor.

5. What are the risks from rotavirus vaccine?

    A vaccine, like any medicine, could possibly cause serious 
problems, such as severe allergic reactions. The risk of any vaccine 
causing serious harm, or death, is extremely small.
    Most babies who get rotavirus vaccine do not have any problems with 
it.
     Babies might become irritable, or have mild, temporary 
diarrhea or vomiting after a dose of rotavirus vaccine.
     Rotavirus vaccine does not appear to cause any serious 
side effects.

6. What if there is a moderate or 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 http://www.vaers.hhs.gov, or by calling 1-800-822-7967.
    VAERS does not provide medical advice.

7. The National Vaccine Injury Compensation Program

    The National Vaccine Injury Compensation Program (VICP) was created 
in 1986.
    Persons who believe they may have been injured by a vaccine can 
learn about the program and about filing a claim by calling 1-800-338-
2382 or visiting the VICP Web site at http://www.hrsa.gov/vaccinecompensation.

8. How can I learn more?

     Your provider 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) or
--Visit CDC's Web site at http://www.cdc.gov/vaccines.

    Department of Health and Human Services, Centers for Disease 
Control and Prevention, Vaccine Information Statement, Rotavirus 
Vaccine, (00/00/0000) (Proposed), 42 U.S.C. 300aa-26.

    Dated: August 3, 2010.
Tanja Popovic,
Deputy Associate Director for Science, Centers for Disease Control and 
Prevention.
[FR Doc. 2010-19782 Filed 8-10-10; 8:45 am]
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