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Get the free Emergency Use Authorization of Peramivir IV Fact Sheet for Health Care Providers - fda

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This document contains detailed information about the emergency use authorization of Peramivir IV for the treatment of 2009 H1N1 infection, including dosage, administration guidelines, contraindications,
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How to fill out Emergency Use Authorization of Peramivir IV Fact Sheet for Health Care Providers

01
Obtain the Emergency Use Authorization of Peramivir IV Fact Sheet template.
02
Read through the entire fact sheet carefully to understand the information required.
03
Fill out the provider's details, including the facility name, address, and contact information.
04
Provide patient's information including name, age, and medical history as relevant.
05
Indicate the indication for use of Peramivir IV in the treatment of the patient.
06
Document any known allergies or contraindications related to the use of Peramivir IV.
07
Include dosing information and administration details as per the guidelines.
08
Complete the section on monitoring and follow-up care for the patient.
09
Sign and date the fact sheet to authenticate the information provided.

Who needs Emergency Use Authorization of Peramivir IV Fact Sheet for Health Care Providers?

01
Health care providers administering Peramivir IV for treating eligible patients.
02
Healthcare facilities that require a standardized guideline for the use of Peramivir IV.
03
Patients diagnosed with severe influenza who may benefit from Peramivir IV treatment.
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People Also Ask about

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.
There are four FDA-approved antiviral drugs recommended by CDC to treat flu this season.
(Nasdaq: BCRX) today announced that the U.S. Food and Drug Administration (FDA) has approved a supplemental new drug application for RAPIVAB® (peramivir injection) expanding the patient population of RAPIVAB for the treatment of acute uncomplicated influenza to include patients six months and older who have been
Intravenous Administration Dilute the appropriate dose of peramivir 10 mg/mL solution to a final concentration between 1 and 6 mg/mL. Acceptable diluents include 0.9% or 0.45% Sodium Chloride Injection, 5% Dextrose Injection, or Lactated Ringer's Injection. Adults: Dilute to a maximum volume of 100 mL.
Contraindications. 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.
Peramivir is used safely and efficiently in hospitalized adult and pediatric patients with suspected or laboratory-confirmed influenza.

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The Emergency Use Authorization (EUA) of Peramivir IV Fact Sheet for Health Care Providers provides guidance on the use of Peramivir, an antiviral medication, during public health emergencies when conventional treatments are unavailable.
Health care providers who intend to administer Peramivir IV under the EUA are required to file and follow the guidelines outlined in the Fact Sheet.
Health care providers should fill out the Fact Sheet by providing necessary patient information, noting indications for use, and ensuring compliance with the emergency use provisions as described in the document.
The purpose of the Fact Sheet is to inform health care providers about the safe and effective use of Peramivir IV during emergencies, detailing its indications, administration methods, and potential side effects.
The information that must be reported includes patient demographics, details of treatment administration, any observed side effects, and outcomes associated with the therapy.
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