Drug updated on 9/4/2024
Dosage Form | Injection (intravenous: 200 mg/20 mL [10 mg/mL]) |
Drug Class | Influenza virus neuraminidase inhibitors |
Ongoing and Completed Studies | ClinicalTrials.gov |
Indication
- Indicated for the treatment of acute uncomplicated influenza in patients 6 months and older who have been symptomatic for no more than two days.
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Summary
- Rapivab (peramivir) is indicated for the treatment of acute uncomplicated influenza in patients 6 months and older who have been symptomatic for no more than two days.
- This summary is based on the review of 10 systematic review(s)/meta-analysis(es). [1-10]
- Oseltamivir (300 mg/day for 5 days) reduced time to fever alleviation by -19.1 hours compared to placebo. Baloxavir (40 mg/day) reduced time to symptom alleviation by -28.2 hours. Peramivir (300 mg/day) reduced time to resumption of usual activities by -43.5 hours. Peramivir (300 mg single dose) reduced time to symptom alleviation by -17.68 hours; 600 mg Peramivir by -16.15 hours. Zanamivir and Oseltamivir also showed efficacy with mean differences between 12.78 to 19.51 hours.
- Baloxavir and neuraminidase inhibitors (NAIs) reduced time to clinical resolution by -21.3 hours and decreased influenza-related complications (OR: 0.55). Peramivir showed higher efficacy in time to alleviation of symptoms (TTAS) with a mean difference (MD) of -11.214 hours. Baloxavir had significantly greater virus titer reduction in high-risk patients compared to Oseltamivir and Peramivir.
- Baloxavir and NAIs reduced incidences of bronchitis, sinusitis, acute otitis media, and antibiotic prescriptions, with trends suggesting reduced pneumonia and hospitalization rates.
- Peramivir demonstrated higher efficacy in TTAS compared to Baloxavir and Laninamivir, with Zanamivir associated with the shortest TTAS among treatments. Baloxavir showed superior antiviral activity, particularly in high-risk patients, with overall efficacy comparable to other NAIs.
- Baloxavir demonstrated a lower incidence of AEs (5.1%) compared to neuraminidase inhibitors (NAIs) (11%) and placebo (8.9%). Baloxavir was associated with the lowest risk of total adverse events.
- Oseltamivir was linked to increased occurrences of nausea and vomiting, with NAIs showing a significant increase in these symptoms (OR: 1.61). Peramivir had a similar incidence of AEs (RR = 1.023) and serious AEs (RR = 1.068) as Oseltamivir.
- Baloxavir presented a similar safety profile to other antivirals and had a lower risk of drug-related adverse events in high-risk patients.
- Oseltamivir, Baloxavir, Peramivir, Zanamivir, and Laninamivir were evaluated for efficacy and safety in healthy young and middle-aged adults with seasonal influenza, high-risk patients, and otherwise healthy patients, showing comparable efficacy across these groups, with Baloxavir demonstrating superior antiviral activity in high-risk patients.
Product Monograph / Prescribing Information
Document Title | Year | Source |
---|---|---|
Rapivab (peramivir) prescribing information. | 2022 | BioCryst Pharmaceuticals, Inc., Durham, NC |
Systematic Reviews / Meta-Analyses
Clinical Practice Guidelines
Document Title | Year | Source |
---|---|---|
2020-2021 AMMI Canada guidance on the use of antiviral drugs for influenza in the setting of co-circulation of seasonal influenza and SARS-CoV-2 viruses in Canada. | 2020 | Journal of the Association of Medical Microbiology and Infectious Disease Canada |