Entry last updated: May 27, 2004
- Understanding the Disease
- Available Vaccines
- History of the Vaccine
- Who Should and Should Not Receive the Vaccine
- Dose Schedule
- Effectiveness of the Vaccine
- Known Side Effects
- Related Issues
- Key References and Sources of Additional Information
Understanding the Disease
Influenza can affect anyone, and epidemics of influenza occur during the winter months nearly every year. Influenza is spread through coughing and sneezing, and is highly contagious, especially in childcare centers, schools, and nursing homes.
Influenza generally comes on suddenly, and symptoms include muscle aches, fever, chills, headache, cough, and runny nose. Young infants may develop croup. The most frequent complication of flu is pneumonia. Myocarditis (inflammation of the heart) and worsening of chronic lung diseases also may occur.
On average, influenza causes approximately 36,000 deaths and 148,000 hospitalizations each year in the United States. More than 90% of influenza-related deaths are in people aged 65 years or older.
Manufacturer: MedImmune Vaccines��
Manufacturer: Chiron Corporation
Year Licensed: 1988
Manufacturer: Aventis Pasteur
Year Licensed: 1978
FluMist� does not contain thimerosal. Both Fluvirin� and Fluzone� are available with reduced thimerosal formulation. For information on the thimerosal content in these vaccines, see the Food and Drug Administration at www.fda.gov/cber/vaccine/thimerosal.htm#t3 or Johns Hopkins University's Institute for Vaccine Safety at
History of the Vaccine
Influenza vaccines have been used since 1945. Each year, the vaccines contain three virus strains that are expected to affect the United States in the upcoming winter.
Until recently, all available influenza vaccines�were trivalent inactivated (killed) virus vaccines (TIV). In spite of common belief, inactivated vaccines cannot cause�influenza. In June of 2003, a live, attenuated, cold adapted, temperature sensitive, trivalent influenza virus vaccine (LAIV) was licensed in the United States. The temperature sensitive type A and B strains of influenza virus contained in LAIV replicate (multiply) in the nasal passages but not in the lower repiratory tract.
TIV came in whole-virus and split-virus forms prior to 2001; however, because of fewer side effects, including fever and reactions at the injection site, only split-virus vaccines are currently available in the U.S. Due to the change in the types of virus circulating each year, some of the components of the influenza vaccine must be changed as well. The�LAIV contains no preservatives and is licensed for use in persons ages 5 to 49 years.
Who Should and Should Not Receive this Vaccine
Who should receive the TIV each year?
People (including children over six months of age) at increased risk of developing complications from flu, including those who:
- Are 50 years old or older (especially those 65 and older)
- Live in nursing homes or other long-term care facilities
- Have long-term disorders of the lungs, heart, or circulation (including asthma or cystic fibrosis)
- Have metabolic diseases (including diabetes)
- Have kidney disorders
- Have blood disorders (including anemia or sickle cell disease)
- Have weakened immune systems (including immunosuppression caused by medications, malignancies, organ transplant, or HIV infection)
- Are children who receive long-term aspirin therapy (and therefore have a higher chance of developing Reye syndrome if infected with influenza)
- Are women who will be in the second or third trimester of pregnancy during the influenza season (November to April)
- Starting in the 2004/2005 influenza season, it is recommended that children ages 6 to 23 months receive TIV.
Who else should receive an influenza vaccine each year?
People who can transmit influenza viruses to those at high risk for complications, including:
- Health care providers
- Employees of nursing homes or assisted living facilities, and providers of home care to people in high-risk groups
- Emergency response workers
- Children who are members of households with high-risk persons
In addition, an influenza vaccine is encouraged for healthy people six months of age or older, who:
- Plan to travel to foreign countries and areas where flu outbreaks may be occurring, such as the Tropics and the Southern Hemisphere from April through September
- Travel as a part of large organized tourist groups that may include persons from areas of the world where flu viruses are circulating
- Attend school or college and reside in dormitories, or reside in institutional settings
- Wish to reduce their risk of becoming ill with influenza
Women who are breastfeeding may receive the vaccine. TIV does not affect the safety of mothers who are breastfeeding or the safety of their infants. It is not known if LAIV is excreted in human milk, therefore, caution is recommended.
Who should not receive influenza vaccine:
- Infants younger than six months of age
- Children younger than four years of age should not receive Fluvirin�1 (Chiron Corp.) because it has not been proven effective for them.
- Children younger than five years of age and adults over 49 years of age should not receive LAIV because safe use in these age groups has not been established.
- LAIV should not be given to children and adolescents (5-17 years of age) receiving aspirin or aspirin-containing medications, because of the complications associated with aspirin and wild-type influenza infection in this age group.
- People with a history of asthma or other reactive airway diseases should not be given LAIV because the safety of LAIV in people with a history of these problems has not been established.
- People with chronic underlying medical conditions that may predispose them to severe influenza infections should also not be given LAIV. For these people, TIV is indicated.
- LAIV should not be given to pregnant women.
- LAIV should not be given to people with a history of Guillain-Barre syndrome.
- LAIV should not be given concurrently with other live-virus vaccines.
- People who have had an anaphylactic reaction (allergic reactions that cause difficulty breathing, which is often followed by shock) to eggs, egg products, or other components of the flu vaccine. There are antiviral agents which doctors can prescribe as an alternative for preventing influenza in such people.
- People with acute serious illness with fever
- People who are moderately or severely ill should consult with their physician before receiving any vaccine
- Under no circumstances should LAIV be given by injection.
Influenza immunization is recommended by:
- Advisory Committee on Immunization Practices of the Centers for Disease Control and Prevention
- American Academy of Family Physicians
- American Academy of Pediatrics
- American Thoracic Society
The summary of adolescent/adult immunization recommendations can be found at: www.cdc.gov/nip/recs/adult-schedule.pdf
1 NNii uses vaccine trade names only for clarity in our presentation of immunization recommendations. NNii does not recommend specific vaccine brands over others.
When young children (six months until nine years old) are vaccinated against influenza for the first time, they should receive two doses of age-appropriate influenza vaccine given one month apart. For children 6-35 months of age, �a half dose (0.25 ml) of�TIV (injected)�is�recommended, �in contrast to 0.5 ml which is the usual dose for everyone over�three years of age. In the United States,�Fluzone� (Aventis Pasteur) may be administered to children as young as six months of age, but Fluvirin� (Chiron Corp.) should only be given to children four years of age and older because its efficacy�in younger people has not been demonstrated. LAIV should only be given to healthy children and adolescents, ages 5-17 years, and healthly adults, ages 18-49.
When indicated, people nine years old or older should receive one dose of influenza vaccine each year. Ideally, people should receive their influenza vaccine from the beginning of October through November each year, prior to the influenza season, which generally peaks during late December through early March. However, vaccination later in the season is considered worthwhile.
Effectiveness of the Vaccine
Each year, the influenza vaccine contains three virus strains, representing the influenza viruses likely to circulate in the United States in the upcoming winter.
When the match between the virus strains in the vaccine and the circulating viruses is close, the vaccine prevents illness in up to 90% of healthy adults under the age of 65. Among elderly people, the vaccine is about 30-70% effective in preventing disease, but it is 50-60% effective in preventing hospitalization and 80% effective in preventing influenza-related death in the elderly.�
The vaccine protects between 45% and 90% of healthy children from getting influenza.� Studies have shown that the older and healthier children who have received the influenza vaccine are, the more likely they will be protected.� Influenza vaccination has also been shown to decrease middle ear infections among young children by about 30%.
Known Side Effects
The majority of those immunized with TIV will have no adverse reactions. Of those who do have a side effect, most will have soreness or tenderness at the injection site. Fewer than 1% of�adults immunized will also experience fever, chills, or a general sense of feeling unwell that lasts one to two days.� Children are more likely to experience these symptoms.
In very rare cases (far less than 1 out of 10,000), serious reactions can occur. People who have an allergy to eggs (which are used in making the vaccine) or any component of the vaccine are at greater risk for a serious allergic reaction.� If you or your child has developed hives or swollen lips or tongue; has had trouble breathing; or has collapsed after eating eggs or receiving a previous dose of influenza vaccine, consult with your healthcare provider to see if the vaccine should be given.�
Because of a slight increase in the frequency of Guillain-Barre Syndrome [GBS]�(a progressive disorder affecting the nervous system) associated with the 1976 swine flu vaccine, subsequent flu vaccines have been closely monitored. It has been estimated that about one case of GBS may occur per million persons immunized with TIV, although these cases may not berelated to TIV.�If a person is not at high�risk for getting complications from influenza, a person who developed GBS within six weeks of a previous influenza shot should avoid subsequent influenza shots. If the risk from influenza is high, they should be vaccinated with an age-appropriate inactivated influenza vaccine because the�established�benefits of the vaccine�justify vaccination.�LAIV should not be given to individuals who have a history of GBS because safety in those persons has not been investigated.
Influenza vaccines given as a nasal spray are being used for adults in Russia, and have been under development in the U.S. since the 1960's. LAIV administered as a nasal spray was approved by the FDA in June of 2003. It is the first nasally administered vaccine to be marketed in the United States and the first live virus influenza vaccine approved in the U.S. The possible�advantages of this type of vaccine are that it is easy to administer, has the potential to induce a broad mucosal and systemic�immune response, and�has been shown to be approximately 87% effective in children. Although TIV and LAIV appear to have similar effectiveness and safety profiles, no study has directly compared the efficacy or effectiveness of TIV and trivalent LAIV.
When there is a major change in the influenza virus strain from one year to the next, epidemics or pandemics (world outbreaks) can occur. During the 20th century, there were four major pandemics; the worst caused 21 million deaths worldwide and 500,000 deaths in the U.S. from 1918 to 1919. Between 1957 and 1986 there were 19 different flu epidemics in the U.S.; several of the most recent caused more than 40,000 deaths.
Key References and Sources of Additional Information
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Including available vaccines, history of the vaccine, who should and should not receive it, dose schedules, effectiveness, known side effects, and related issues.