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Pfizer Inc pfizer s rsvpref vaccine abrysvo
Pfizer S Rsvpref Vaccine Abrysvo, supplied by Pfizer Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rsvpref+abrysvo/bivalent+bnt+pfizer+vaccine/pmc13253500-153-0-0
Average 86 stars, based on 1 article reviews
pfizer s rsvpref vaccine abrysvo - by Bioz Stars, 2026-09
86/100 stars

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Control:

Article Title: Postmarketing safety surveillance for GSK's AS01 E -adjuvanted respiratory syncytial virus prefusion F protein-based vaccine in the USA: protocol for a non-interventional postauthorisation safety study.
Article Snippet: .. Vaccinees will be required to have ≥365 days of continuous medical and prescription drug benefits prior to index (enrolment gaps ≤45 days within the 365 days are permitted), no evidence of a second dose of adjuvanted RSVPreF3 throughout the risk and control windows, or other products used for RSV disease prevention, such as Pfizer’s RSVPreF (Abrysvo) or Moderna’s modified mRNA RSVPreF (MRESVIA) vaccinations, at any time prior to the index date or throughout the risk and control windows. ..

Modification:

Article Title: Postmarketing safety surveillance for GSK's AS01 E -adjuvanted respiratory syncytial virus prefusion F protein-based vaccine in the USA: protocol for a non-interventional postauthorisation safety study.
Article Snippet: .. Vaccinees will be required to have ≥365 days of continuous medical and prescription drug benefits prior to index (enrolment gaps ≤45 days within the 365 days are permitted), no evidence of a second dose of adjuvanted RSVPreF3 throughout the risk and control windows, or other products used for RSV disease prevention, such as Pfizer’s RSVPreF (Abrysvo) or Moderna’s modified mRNA RSVPreF (MRESVIA) vaccinations, at any time prior to the index date or throughout the risk and control windows. ..

other:

Article Title: Correction: Anastassopoulou et al. Development, Current Status, and Remaining Challenges for Respiratory Syncytial Virus Vaccines. Vaccines 2025, 13 , 97.
Article Snippet: Consequent to these changes, the last two sentences of the fourth paragraph in Section 5.1.2, “RSVPreF (Abrysvo, Pfizer)”, should be replaced with the following: “This overview of the available data indicates that, although it is not currently recommended, revaccination may be needed for protection against RSV-LRTD in the seasons to come, independently of which RSV vaccine is used [52].” The last sentence of the fifth paragraph in Section 5.1.2 of the original publication should be changed simply to “the GBS reports were 4.4 cases per million administered doses of Abrysvo [59]” because the increased incidence of GBS following RSVPreF was not statistically significant.

Article Title: Addressing the Underestimated Burden of RSV in Older Adults in Europe: Epidemiology, Surveillance Gaps, and Public Health Implications.
Article Snippet: Specifically, RSVPreF3 (Arexvy, GSK) has been approved by regulatory bodies for the following indications: adults aged 50–59 years at increased risk of RSV disease, and all adults aged ≥60 years; RSVPreF (Abrysvo, Pfizer) has been approved by FDA for adults aged 18–59 years at increased risk of severe disease; all adults aged ≥60 years, and pregnant individuals at 32–36 weeks of gestation to protect infants from birth up to 6 months.

Article Title: Adult vaccinations against respiratory infections.
Article Snippet: The RSVpreF (Abrysvo, Pfizer) is a subunit vaccine based on the prefusion F protein.

Article Title: Effectiveness and Safety of Respiratory Syncytial Virus Vaccine for US Adults Aged 60 Years or Older.
Article Snippet: The estimated excess of GBS cases associated with the RSVPreF (Abrysvo, Pfizer) vaccine was 18.2 per 1 000 000 vaccines administered, and for the RSVPreF3+AS01 vaccine (Arexvy, GBS), the estimated excess of GBS cases was 5.2 per 1 000 000 vaccinations.

Article Title: Adult vaccinations against respiratory infections.
Article Snippet: More recently, the CDC published a Morbidity and Mortality Weekly Report (MMWR) confirming that the safety of the RSVpreF (Abrysvo, Pfizer) and the RSVPreF3 OA (Arexvy, GSK) vaccines was consistent with the vaccine data reported in the clinical trials among adults aged ≥60 years [96].



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