Brand Name

Rapivab

Generic Name
Peramivir
View Brand Information
FDA approval date: December 20, 2014
Form: Solution

What is Rapivab (Peramivir)?

When influenza strikes, it can leave people bedridden with fever, chills, muscle aches, and exhaustion often disrupting work, school, and family life. For some, especially those with weakened immune systems or underlying health conditions, the flu can become far more serious, even life-threatening. Rapivab (peramivir) is a prescription antiviral medication designed to help patients recover faster from the flu and reduce its severity. 

Rapivab belongs to a class of medications called neuraminidase inhibitors, which also includes oseltamivir (Tamiflu) and zanamivir (Relenza). What sets Rapivab apart is its intravenous (IV) formulation, allowing healthcare providers to administer it directly into the bloodstream for fast, effective treatment often in a single dose. It’s an important option for patients who cannot take oral medications or need rapid antiviral action, such as those hospitalized with acute influenza symptoms. 

What does Rapivab do? 

Rapivab is used to treat acute uncomplicated influenza (flu) in adults and children aged 6 months and older who have had symptoms for no more than two days. The medication helps shorten the duration of flu symptoms and may reduce the risk of complications when given early in the illness. 

In clinical studies, Rapivab has been shown to reduce the length and intensity of flu symptoms by about one day compared to placebo (FDA, 2023). This might seem modest, but for patients at high risk such as older adults, pregnant women, or people with chronic diseases timely antiviral treatment can make a significant difference in recovery and comfort. 

Rapivab is not a substitute for the annual flu vaccine, but it plays a vital role when infection occurs despite vaccination or when immediate antiviral therapy is needed. Doctors may also use it in certain severe or hospitalized cases when oral antivirals are not suitable. 

How does Rapivab work? 

Rapivab contains peramivir, which targets the neuraminidase enzyme, a key protein found on the surface of influenza viruses. When a virus infects a person, it multiplies inside cells and then uses this enzyme to release new virus particles, allowing the infection to spread throughout the body. 

By blocking the neuraminidase enzyme, Rapivab prevents the virus from escaping infected cells, effectively stopping it from spreading further. This containment allows the immune system to catch up, helping the body clear the infection faster. 

Clinically, this mechanism is important because it reduces viral load, the amount of virus in the body which can lead to milder symptoms and a quicker recovery. The intravenous route allows Rapivab to reach therapeutic levels in the bloodstream quickly, making it especially useful for patients who are vomiting, unconscious, or unable to swallow pills. 

Rapivab side effects 

Like all medications, Rapivab can cause side effects, though most are mild and temporary. Understanding these effects helps patients and caregivers feel confident and prepared during treatment. 

Common side effects may include: 

  • Diarrhea 
     
  • Constipation 
     
  • Insomnia or trouble sleeping 
     
  • Cough or mild throat irritation 

These symptoms are typically short-lived and resolve as the body adjusts. 

Serious but uncommon side effects include: 

  • Allergic reactions such as rash, itching, or swelling 
     
  • Shortness of breath or difficulty breathing 
     
  • Confusion, hallucinations, or unusual behavior (rare but reported with antiviral drugs for influenza) 
     
  • Liver problems, indicated by yellowing of the skin or eyes (jaundice) 

If any severe reaction occurs, patients should seek immediate medical attention. 

Use Rapivab cautiously or avoid if you have severe kidney disease or allergies to peramivir or other neuraminidase inhibitors. It’s generally safe under medical supervision, with uncommon side effects, and aids flu recovery. 

Rapivab dosage 

Rapivab is a rapid, single-dose IV infusion (15-30 min) for flu, given in clinical settings. It’s typically for those who can’t take oral medication, have severe flu needing hospital care, or require a quick antiviral dose. Dosage may be adjusted for kidney impairment. 

Before Rapivab administration, kidney function and overall health are assessed for safe dosing. Patients should not self-administer. Post-infusion, doctors monitor for rare allergic reactions. The treatment is generally well-tolerated, usually requiring a single infusion. 

Does Rapivab have a generic version? 

As of 2025, Rapivab (peramivir) does not have a generic version approved in the United States. It is marketed by BioCryst Pharmaceuticals and remains available only under its brand name. However, international versions may exist in other markets. 

While peramivir is an internationally recognized active ingredient and may be available generically elsewhere, a U.S. FDA-approved generic would meet the same strict standards as the brand name. As Rapivab is typically a single-dose hospital treatment, the lack of a generic doesn’t significantly affect access, as insurance or hospital programs usually cover it for severe influenza. 

Conclusion 

Rapivab (peramivir) offers a fast, effective, and convenient way to treat influenza in patients who need hospital-based care or cannot take oral medications. By targeting the virus directly and preventing its spread within the body, it helps shorten illness duration, reduce symptom severity, and support quicker recovery. 

Rapivab’s single-dose IV format offers a practical advantage for patients needing immediate treatment or those with difficulty taking oral antivirals. While side effects can occur, they are generally mild and manageable under professional supervision. As a reliable antiviral option, Rapivab provides healthcare providers with another tool to protect patients, especially those at high risk of complications. When prescribed and monitored appropriately, Rapivab is a safe and effective therapy that aids faster recovery and promotes confident return to health. 

References 

  1. U.S. Food and Drug Administration (FDA). (2023). Rapivab (peramivir) prescribing information. Retrieved from https://www.accessdata.fda.gov 
     
  1. Mayo Clinic. (2024). Peramivir (intravenous route): Description and precautions. Retrieved from https://www.mayoclinic.org 
     
  1. MedlinePlus. (2024). Peramivir injection: Uses and side effects. National Library of Medicine. Retrieved from https://medlineplus.gov 
     
  1. Centers for Disease Control and Prevention (CDC). (2024). Antiviral drugs for influenza: Summary for clinicians. Retrieved from https://www.cdc.gov 

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Brand Information

Rapivab (peramivir)
1INDICATIONS AND USAGE
RAPIVAB is indicated for the treatment of acute uncomplicated influenza in patients 6 months and older who have been symptomatic for no more than 2 days.
2DOSAGE FORMS AND STRENGTHS
Each vial of RAPIVAB injection contains 200 mg per 20 mL (10 mg per mL) as a clear, colorless solution
3CONTRAINDICATIONS
RAPIVAB is contraindicated in patients with known serious hypersensitivity or anaphylaxis to peramivir or any component of the product. Severe allergic reactions have included anaphylaxis, erythema multiforme, and Stevens-Johnson syndrome
4ADVERSE REACTIONS
The following adverse reactions are discussed in other sections of the labeling:
  • Serious skin and hypersensitivity reactions
  • Neuropsychiatric events
4.1Clinical Trials Experience
Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.
4.2Postmarketing Experience
The following additional adverse reactions have been identified during postapproval use of RAPIVAB. Because postmarketing reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.
Dermatologic: Stevens-Johnson syndrome, exfoliative dermatitis, rash
General Disorders and Administration Site Conditions: Anaphylactic/anaphylactoid reactions
Psychiatric: Abnormal behavior, hallucination
5DRUG INTERACTIONS
This section describes clinically relevant drug interactions with RAPIVAB. Drug-drug interaction studies are described elsewhere in the labeling
5.1Influenza Vaccines
Inactivated influenza vaccine can be administered at any time relative to use of RAPIVAB. For live attenuated influenza vaccine (LAIV), antiviral drugs may inhibit viral replication and thus may reduce vaccine efficacy. The concurrent use of RAPIVAB with LAIV intranasal has not been evaluated. Because of the potential for interference between these two products, avoid use of LAIV within 2 weeks before or 48 hours after administration of RAPIVAB unless medically indicated.
6OVERDOSAGE
There is no human experience of acute overdosage with RAPIVAB. Treatment of overdosage with RAPIVAB should consist of general supportive measures including monitoring of vital signs and observation of the clinical status of the patient. There is no specific antidote for overdose with RAPIVAB.
RAPIVAB is cleared by renal excretion and can be cleared by hemodialysis.
7DESCRIPTION
RAPIVAB (peramivir) is an inhibitor of influenza virus neuraminidase. The chemical name is (1S,2S,3R,4R)-3-[(1S)-1-(acetylamino)-2-ethylbutyl]-4-(carbamimidoylamino)-2-hydroxycyclopentanecarboxylic acid, trihydrate. The chemical formula is C
Chemical Structure
RAPIVAB injection is a clear, colorless, sterile, isotonic solution (200 mg per 20 mL) in glass vials fitted with rubber stoppers and royal blue flip-off seals. Each mL contains 10 mg peramivir (on an anhydrous basis) in 0.9% sodium chloride solution. The pH may have been adjusted with sodium hydroxide, USP and/or hydrochloric acid, USP. The pH is 5.5 to 8.5.
8HOW SUPPLIED/STORAGE AND HANDLING
RAPIVAB injection is a clear, colorless sterile, isotonic solution. Each single-use vial contains 200 mg per 20 mL (10 mg/mL) of peramivir in a clear glass vial (NDC # 72769-181-01). RAPIVAB injection is supplied in cartons containing 3 single-use vials (NDC # 72769-181-03).
9PATIENT COUNSELING INFORMATION
Advise patients of the following:
  • There is a risk of severe allergic reactions (including anaphylaxis) or serious skin reactions with RAPIVAB use. Advise patients to seek immediate medical attention if an allergic-like reaction occurs or is suspected
  • There is a risk of neuropsychiatric events in patients with influenza. Patients should contact their physician if they experience signs of abnormal behavior after receiving RAPIVAB
10PRINCIPAL DISPLAY PANEL - 200 mg/20 mL Vial Carton
Rx Only
NDC 72769-181-03
Rapivab
200 mg/20 mL per vial
For Intravenous
Carton contains 3 vials
PRINCIPAL DISPLAY PANEL - 200 mg/20 mL Vial Carton