IMPORTANT SAFETY INFORMATION AND INDICATION
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IMPORTANT SAFETY INFORMATION
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Severe allergic reaction (eg, anaphylaxis) to any component of Prevnar 13® or any diphtheria toxoid–containing vaccine is a contraindication
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Immunocompromised individuals or individuals with impaired immune responsiveness due to the use of immunosuppressive therapy may have reduced antibody response
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In adults, the most commonly reported solicited adverse reactions were pain, redness, and swelling at the injection site, limitation of arm movement, fatigue, headache, muscle pain, joint pain, decreased appetite, vomiting, fever, chills, and rash
INDICATION
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In adults 18 years of age and older, Prevnar 13® is indicated for active immunization for the prevention of pneumonia and invasive disease caused by Streptococcus pneumoniae serotypes 1, 3, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, 19F, and 23F
Limitations of Use and Effectiveness
- Prevnar 13® will only help protect against S. pneumoniae serotypes in the vaccine
Patients should always ask their doctors for medical advice about adverse events. You are encouraged to report negative side effects of vaccines to the US Food and Drug Administration (FDA) and the Centers for Disease Control and Prevention (CDC). Visit www.vaers.hhs.gov or call
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Manufactured by Wyeth Pharmaceuticals LLC
© 2020 Pfizer Inc.
All rights reserved.
Marketed by Pfizer Inc.
March 2020

Manufactured by Wyeth Pharmaceuticals LLC. Marketed by Pfizer Inc.
© 2020 Pfizer Inc. All rights reserved.
March 2020
