This site is intended for U.S. healthcare professionals.

Visit Pfizer Medical

Menu

Close

Sign InLog Out
ProductsOrderMaterialsCo-pay Cards & Patient Savings OffersRequest SamplesHospital ProductsVaccinesPatient AssistancePfizer Oncology TogetherPfizer RxPathwaysExplore ContentEventsMaterialsVideosContact

Menu

Close

HomeCDC RecommendationAbout RSVAbout ABRYSVOOrder ABRYSVOAccess & SupportAccess & SupportHealth Plan CoverageRequest a RepEventsMaterialsVideos
Prescribing InformationIndicationsPatient SiteMaternal
EVERY BREATH THEY TAKE MATTERS. EVERY BREATH THEY TAKE MATTERS.
ABRYSVOTM: CDC-recommended for the prevention of RSV in adults aged 60 years
and older4,5*

RSV won't wait. Vaccinate today.
 Press Release Loading CDC RecommendationLoading Press Release Loading View Clinical DataLoading Press ReleaseLoading CDC RecommendationLoading Press ReleaseLoading View Clinical DataLoadingReferencesUsing shared clinical decision-making.Estimated based on average respiratory rates from birth to age 60.1-3
Discover ABRYSVO
Discover ABRYSVO

ABRYSVO is a vaccine indicated for the prevention of LRTD caused by RSV in adults aged 60 years and older.4

 ABRYSVO Data

Explore the efficacy and safety profile of ABRYSVO
 

 Learn MoreLoading ABRYSVO Reconstitution

See Pfizer's convenient, needle-free‡ reconstitution kit

‡Needle required for intramuscular injection is not included.

 Learn MoreLoading Accessing ABRYSVO

Learn more about costs and coverage, and get the support you need
 

 See DetailsLoading
~79 million older adults are at risk for RSV.6,7
Help prevent RSV with CDC-recommended ABRYSVO.4,5
Vaccinate your patients aged 60 years and older today5
  • These adults may receive a single dose of the vaccine based on discussions with their healthcare provider*—as early as vaccine supply becomes available
  • For the 2023-2024 season, offer vaccination to your patients aged 60 years and older
*Using shared clinical decision-making.

View MMWR Publication

CDC=Centers for Disease Control and Prevention; LRTD=lower respiratory tract disease; MMWR=Morbidity and Mortality Weekly Report; RSV=respiratory syncytial virus.

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

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: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. 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.United States Census Bureau. Annual estimates of the resident population for selected age groups by sex for the United States: April 1, 2020 to July 1, 2022. Accessed June 28, 2023. https://www.census.gov/data/tables/time-series/demo/popest/2020s-national-detail.htmlCarvajal JJ, Avellaneda AM, Salazar-Ardiles C, Maya JE, Kalergis AM, Lay MK. Host components contributing to respiratory syncytial virus pathogenesis. Front Immunol. 2019;10:2152.

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

Pfizer for Professionals 1-800-505-4426

This site is intended only for U.S. healthcare professionals. The products discussed in this site may have different product labeling in different countries. The information provided is for educational purposes only.

© 2023 Pfizer Inc. All rights reserved.

PP-A1G-USA-0511
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