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ABRYSVO®: CDC-recommended for protection against RSV in adults aged 60 years and older based on shared clinical decision-making1
 View the Clinical Data Loading ReferencesEstimated based on average respiratory rates from birth to age 60.2-4 Rates of systemic AEs similar to placebo in older adults Kicker Header of this card goes here

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Similar rates of systemic AEs observed between ABRYSVO and placebo groups5†

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†The most common solicited local and systemic adverse reactions (≥10%) were fatigue (15.5%), headache (12.8%), pain at the injection site (10.5%), and muscle pain (10.1%).5

 Powerful protection against RSV in older adults‡

86% vaccine efficacy against RSV-LRTD with ≥3 symptoms (96.66% CI: 32.0, 98.7)5
67% vaccine efficacy against RSV-LRTD with ≥2 symptoms (96.66% CI: 28.8, 85.8)5

 View Efficacy Data Additional Data

‡Interim data from season 1. The median duration of efficacy follow-up was 7 months. Evaluable efficacy population: ABRYSVO, n=16,306; placebo, n=16,308.5

Vaccinate your patients aged 60 years and older today with ABRYSVO5

 Vaccine Locator Tool LoadingApproved for 2 Vulnerable Populations

The only RSV vaccine approved for both adults aged 60+ and pregnant individuals (at 32-36 weeks of gestation) for the protection of infants (from birth through 6 months) via maternal immunization5

Learn more about the maternal indication

LoadingABRYSVO Reconstitution

See Pfizer's convenient, needle-free§ reconstitution kit5
§Needle required for intramuscular injection is not included.

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Get the support you need and learn more about costs and coverage

LoadingReferencesAE=adverse event; CDC=Centers for Disease Control and Prevention; LRTD=lower respiratory tract disease; MMWR=Morbidity and Mortality Weekly Report; RSV=respiratory syncytial virus.
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Stay Informed
 Receive Updates About ABRYSVO    Register NowLoading Request a Pfizer Sales Representative  Connect NowLoading

Explore a range of resources related to ABRYSVO, including videos, information about upcoming events, and more.

View Resources
References:Melgar M, Britton A, Roper LE, et al. Use of Respiratory Syncytial Virus Vaccines in Older Adults: Recommendations of the Advisory Committee on Immunization Practices — United States, 2023. MMWR Morb Mortal Wkly Rep. 2023;72(29):793-801.Johns Hopkins Medicine. Vital signs (body temperature, pulse rate, respiration rate, blood pressure). Accessed August 22, 2023. https://www.hopkinsmedicine.org/health/conditions-and-diseases/vital-signs-body-temperature-pulse-rate-respiration-rate-blood-pressureUpToDate. Normal respiratory rate and heart rate in children. Accessed August 12, 2023. https://www.uptodate.com/contents/the-pediatric-physical-examination-general-principles-and-standard-measurements#H10Data on file. Pfizer Inc; August 2023.ABRYSVO (Respiratory Syncytial Virus Vaccine) Prescribing Information. Pfizer Inc; August 2023.

To report an adverse event, please call 1-800-438-1985

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PP-A1G-USA-0936
IndicationsABRYSVO is a vaccine indicated for:
  • active immunization for the prevention of lower respiratory tract disease (LRTD) caused by respiratory syncytial virus (RSV) in individuals 60 years of age and older
  • active immunization of pregnant individuals at 32 through 36 weeks gestational age for the prevention of LRTD and severe LRTD caused by RSV in infants from birth through 6 months of age
Please click here for full Prescribing Information.
Important Safety Information
  • Do not administer ABRYSVO to individuals with a history of a severe allergic reaction (e.g., anaphylaxis) to any component of ABRYSVO
  • A numerical imbalance in preterm births was observed compared to placebo in 2 clinical studies. Data are insufficient to establish or exclude a causal relationship between preterm birth and ABRYSVO. To avoid potential risk of preterm birth with use of ABRYSVO before 32 weeks of gestation, administer to pregnant individuals at 32 through 36 weeks gestational age
  • Appropriate medical treatment must be available in case of an anaphylactic reaction
  • Syncope (fainting) may occur in association with administration of injectable vaccines, including ABRYSVO. Procedures should be in place to avoid injury from fainting
  • Immunocompromised individuals, including those receiving immunosuppressive therapy, may have a diminished immune response to ABRYSVO
  • Vaccination with ABRYSVO may not protect all vaccine recipients
  • In clinical trials with older adults, the most commonly reported (≥10%) adverse reactions were fatigue (15.5%), headache (12.8%), pain at the injection site (10.5%), and muscle pain (10.1%)
  • In clinical trials with pregnant individuals, the most commonly reported (≥10%) adverse reactions were pain at the injection site (40.6%), headache (31.0%), muscle pain (26.5%), and nausea (20.0%)
  • In clinical trials with infants born to pregnant individuals, low birth weight (5.1% ABRYSVO versus 4.4% placebo) and neonatal jaundice (7.2% ABRYSVO versus 6.7% placebo) were observed
Individuals who received ABRYSVO during pregnancy are encouraged to contact 1-800-616-3791 to enroll in a Pregnancy Exposure Registry.

Patients should always ask their healthcare providers 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 http://www.vaers.hhs.gov or call 1-800-822-7967.

Please see full Prescribing Information for ABRYSVO.IndicationsABRYSVO is a vaccine indicated for:
  • active immunization for the prevention of lower respiratory tract disease (LRTD) caused by respiratory syncytial virus (RSV) in individuals 60 years of age and older
     
  • active immunization of pregnant individuals at 32 through 36 weeks gestational age for the prevention of LRTD and severe LRTD caused by RSV in infants from birth through 6 months of age
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