Baloxavir

Brand names: Xofluza
Drug class: Antineoplastic Agents , Antineoplastic Agents

Usage of Baloxavir

Treatment of Seasonal Influenza A and B Virus Infections

Treatment of acute, uncomplicated influenza caused by influenza A or B viruses in adults and adolescents ≥12 years of age who have been symptomatic for ≤48 hours, including those who are otherwise healthy and those who are at high risk for influenza-related complications. Efficacy if administered >48 hours after symptom onset not evaluated.

Data not available to date regarding use for treatment of severe or complicated influenza in hospitalized patients or outpatients.

For treatment of suspected or cOnfirmed acute, uncomplicated seasonal influenza in otherwise healthy outpatients, CDC, IDSA, and others state that any age-appropriate influenza antiviral (oral oseltamivir, inhaled zanamivir, oral Baloxavir marboxil, IV peramivir) can be used if not contraindicated. CDC states may consider early empiric antiviral treatment in outpatients with suspected influenza (e.g., influenza-like illness such as fever with either cough or sore throat) based on clinical judgement if such treatment can be initiated within 48 hours of illness onset.

For treatment of suspected or confirmed seasonal influenza in hospitalized patients or outpatients with severe, complicated, or progressive illness (e.g., pneumonia, exacerbation of underlying chronic medical conditions), CDC states oseltamivir is the preferred influenza antiviral because of lack of data regarding use of other influenza antivirals in such patients. CDC states baloxavir marboxil not recommended for treatment of influenza in hospitalized patients.

Consider that influenza and coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) have overlapping signs and symptoms and coinfection with influenza A or B viruses and SARS-CoV-2 can occur. Although laboratory testing can help distinguish between influenza virus infection and SARS-CoV-2 infection, CDC recommends initiating empiric influenza treatment in patients with suspected influenza who are hospitalized, have severe, complicated, or progressive illness, or are at high risk for influenza complication without waiting for results of influenza testing, SARS-CoV-2 testing, or multiplex molecular assays that detect influenza A and B viruses and SARS-CoV- 2.

Consider viral surveillance data available from local and state health departments and CDC when selecting an antiviral for treatment of seasonal influenza. Strains of circulating influenza viruses and the antiviral susceptibility of these strains constantly evolve, and emergence of resistant strains may decrease effectiveness of influenza antivirals. Although circulating influenza A and B viruses during recent years have been susceptible to baloxavir, consult most recent information on susceptibility of circulating viruses when selecting an antiviral for treatment of influenza.

CDC issues recommendations concerning use of antivirals for treatment of influenza, and these recommendations are updated as needed during each influenza season. Information regarding influenza surveillance and updated recommendations for treatment of seasonal influenza are available from CDC at [Web].

Prevention of Seasonal Influenza A and B Virus Infections

Postexposure prophylaxis of influenza A or B virus infection in adults and adolescents ≥12 years of age who are contacts of an individual with influenza.

Annual vaccination with seasonal Influenza virus vaccine, as recommended by CDC's Advisory Committee on Immunization Practices (ACIP), is the primary means of preventing seasonal influenza and its severe complications. Prophylaxis with an appropriate antiviral active against circulating influenza strains is considered an adjunct to vaccination for control and prevention of influenza in certain individuals.

Base decisions regarding use of antivirals for prophylaxis of seasonal influenza on the risk for influenza-related complications in the exposed individual, the type and duration of contact, recommendations from local or public health authorities, and clinical judgment. In general, use influenza antiviral prophylaxis only if it can be initiated within 48 hours after the most recent exposure.

CDC and others do not recommend routine use of influenza antivirals for postexposure prophylaxis in individuals exposed to influenza; may consider such prophylaxis in certain situations in exposed individuals at high risk for influenza-related complications for whom influenza vaccine is contraindicated, unavailable, or expected to have low efficacy (e.g., immunocompromised individuals).

CDC issues recommendations concerning the use of antivirals for prophylaxis of influenza, and these recommendations are updated as needed during each influenza season. Information regarding influenza surveillance and updated recommendations for prevention of seasonal influenza are available from CDC at [Web].

Relate drugs

How to use Baloxavir

Administration

Oral Administration

Administer orally without regard to meals.

Avoid taking with dairy products; calcium-fortified beverages; or antacids, laxatives, or multivitamins or dietary supplements containing polyvalent cations (aluminum, calcium, iron, magnesium, Selenium, or zinc). (See Specific Drugs under Interactions.)

Commercially available as tablets or as granules for oral suspension that must be suspended in water prior to administration.

Granules for Oral Suspension

Baloxavir marboxil granules for oral suspension are intended for use in patients unable to easily swallow tablets or those requiring enteral administration.

Prior to dispensing, add 20 mL of drinking or sterile water to a bottle containing baloxavir marboxil granules and swirl the bottle to ensure the granules are evenly suspended; do not shake the bottle. Each bottle provides an oral suspension containing 40 mg/20 mL (2 mg/mL) of the drug. Depending on the required dosage, prepare 1 or 2 bottles of the oral suspension.

Does not contain preservatives and must be administered within 10 hours following preparation. May store oral suspension at room temperature (20–25°C) for up to 10 hours after preparation; discard if not used within 10 hours or if stored at a temperature >25°C. Mark the expiration date and time on the bottle at the time of preparation.

Provide a measuring device (e.g., oral syringe, measuring cup) with the oral suspension.

Enteral administration (i.e., feeding tube): Draw the dose of oral suspension into an enteral syringe; flush the feeding tube with 1 mL of water before and after enteral administration of the dose.

Dosage

Pediatric Patients

Treatment of Seasonal Influenza A and B Virus Infections Acute, Uncomplicated Influenza A or B Virus Infections Oral

Adolescents ≥12 years of age weighing <80 kg: Single 40-mg dose given within 48 hours after symptom onset.

Adolescents ≥12 years of age weighing ≥80 kg: Single 80-mg dose given within 48 hours after symptom onset.

Prevention of Seasonal Influenza A and B Virus Infections Oral

Adolescents ≥12 years of age weighing <80 kg: Single 40-mg dose given within 48 hours after contact with an individual with influenza.

Adolescents ≥12 years of age weighing ≥80 kg: Single 80-mg dose given within 48 hours after contact with an individual with influenza.

Adults

Treatment of Seasonal Influenza A and B Virus Infections Acute, Uncomplicated Influenza A or B Virus Infections Oral

Adults weighing 80 kg: Single 40-mg dose given within 48 hours after symptom onset.

Adults weighing ≥80 kg: Single 80-mg dose given within 48 hours after symptom onset.

Prevention of Seasonal Influenza A and B Virus Infections Oral

Adults weighing <80 kg: Single 40-mg dose given within 48 hours after contact with an individual with influenza.

Adults weighing ≥80 kg: Single 80-mg dose given within 48 hours after contact with an individual with influenza.

Special Populations

No special population dosage recommendations provided by the manufacturer for geriatric individuals or patients with impaired hepatic or renal function.

Warnings

Contraindications

  • History of hypersensitivity to baloxavir marboxil or any ingredient in the formulation.

    • Warnings/Precautions

    Sensitivity Reactions

    Serious allergic reactions, including anaphylaxis, anaphylactic or anaphylactoid reactions, angioedema (face, eyelids, tongue, lips), urticaria, and erythema multiforme, reported during postmarketing experience. Rash also reported.

    Initiate appropriate treatment if an allergic-like reaction occurs or is suspected.

    Bacterial Infections

    When making treatment decisions in patients with suspected influenza, consider possibility of primary or concomitant bacterial infection.

    Serious bacterial infections may begin with influenza-like symptoms or may coexist with or occur as complications of influenza. No evidence that baloxavir prevents such complications. If a bacterial infection occurs, treat as appropriate.

    No evidence that baloxavir is effective for illness caused by any organisms other than influenza viruses.

    Immunocompromised Individuals

    Data not available regarding efficacy and safety of baloxavir marboxil for treatment of influenza in individuals with severe immunosuppression. Emergence of resistance to baloxavir may be a concern because duration of influenza virus replication may be prolonged in such patients.

    CDC does not recommend baloxavir marboxil monotherapy for treatment of influenza in individuals with severe immunosuppression.

    Influenza Vaccination

    Influenza antivirals are not a substitute for annual vaccination with a seasonal influenza vaccine (Influenza Virus Vaccine Inactivated, Influenza Vaccine Recombinant, Influenza Vaccine Live Intranasal).

    Although influenza antivirals, including baloxavir marboxil, may be used concomitantly with or any time before or after influenza virus vaccine inactivated or influenza vaccine recombinant, such antivirals may inhibit the vaccine virus contained in influenza vaccine live intranasal and decrease efficacy of the live vaccine. (See Specific Drugs under Interactions.)

    Specific Populations

    Pregnancy

    No adequate and well-controlled studies using baloxavir marboxil in pregnant women to inform a drug-associated risk of adverse developmental outcomes.

    No adverse embryofetal effects were observed in reproduction studies in rats and rabbits.

    Pregnant women are at increased risk for severe complications from influenza, which may lead to adverse pregnancy and/or fetal outcomes including maternal death, stillbirths, birth defects, preterm delivery, low birthweight, and small size for gestational age.

    CDC states baloxavir marboxil not recommended for treatment of influenza in pregnant women because of lack of safety and efficacy data in such patients. Oseltamivir is the preferred antiviral for treatment of suspected or confirmed influenza and prevention of influenza in women who are pregnant or ≤2 weeks postpartum.

    Lactation

    Not known whether distributes into human milk, affects milk production, or has any effects on breast-fed infants. Distributed into milk in rats.

    Manufacturer states consider benefits of breast-feeding and importance of baloxavir marboxil to the woman; also consider potential adverse effects on the breast-fed child from the drug or the underlying maternal condition.

    CDC states baloxavir marboxil not recommended for treatment of influenza in nursing women because of lack of safety data in such patients.

    Pediatric Use

    Safety and efficacy not established in pediatric patients <12 years of age.

    Treatment of acute, uncomplicated influenza in adolescents ≥12 years of age weighing ≥40 kg: Safety and efficacy established in a phase 3, randomized, double-blind, placebo-controlled study. Safety profile was similar to that reported in adults.

    Postexposure prophylaxis of influenza in adolescents ≥12 years of age: Safety and efficacy supported by a randomized, double-blind, placebo-controlled trial conducted in Japan that included 12 individuals 12–17 years of age who received the drug. Adverse effects were similar to those reported in adults who received the drug.

    Geriatric Use

    Safety and efficacy in adults ≥65 years of age for treatment of acute, uncomplicated influenza established and supported by a randomized, double-blind, controlled trial that included 209 adults in this age group at high risk of influenza-related complications who were treated with the drug. Safety profile in adults ≥65 years of age was similar to that reported in the overall trial population, with the exception of nausea (reported in 6% of adults ≥65 years of age compared with 1% of those 18–64 years of age).

    Common Adverse Effects

    GI effects (nausea, diarrhea), bronchitis, sinusitis, headache.

    What other drugs will affect Baloxavir

    Active metabolite of baloxavir marboxil, baloxavir, is metabolized principally by UGT1A3 and, to a minor extent, by CYP3A4.

    Baloxavir marboxil and baloxavir do not inhibit CYP1A2, 2B6, 2C8, 2C9, 2C19, or 2D6 and do not induce CYP1A2, 2B6, or 3A4 in vitro.

    Baloxavir marboxil and baloxavir do not inhibit UGT1A1, 1A3, 1A4, 1A6, 1A9, 2B7, or 2B15 in vitro. Baloxavir does not inhibit organic anion transport polypeptide (OATP) 1B1, OATP1B3, organic cation transporter (OCT) 1, OCT2, organic anion transporter (OAT) 1, OAT3, multidrug and toxin extrusion (MATE) 1, or MATE2K.

    Baloxavir marboxil and baloxavir are substrates of P-glycoprotein (P-gp) in vitro.

    Specific Drugs

    Drug

    Interaction

    Comments

    Antacids, aluminum-, calcium-, or magnesium-containing

    May decrease baloxavir concentrations and decrease efficacy

    Avoid concomitant administration with baloxavir marboxil

    Calcium supplements

    May decrease baloxavir concentrations and decrease efficacy

    Avoid concomitant administration with baloxavir marboxil

    Digoxin

    No effect on pharmacokinetics of digoxin

    Influenza vaccines

    Influenza virus vaccine inactivated (IIV) and influenza vaccine recombinant (RIV): Baloxavir not expected to affect vaccine efficacy; no specific studies

    Influenza vaccine live intranasal (LAIV): Baloxavir may inhibit the vaccine virus and decrease efficacy of the live vaccine; no specific studies; based on its long half-life, ACIP states baloxavir marboxil may interfere with LAIV if given from 17 days before through 2 weeks after the live vaccine

    IIV or RIV: May administer concomitantly with or any time before or after baloxavir

    LAIV: If baloxavir marboxil administered from 17 days before to 2 weeks after LAIV, ACIP recommends revaccination using age-appropriate IIV or RIV

    Iron preparations

    May decrease baloxavir concentrations and decrease efficacy

    Avoid concomitant administration with baloxavir marboxil

    Itraconazole

    No effect on pharmacokinetics of baloxavir marboxil or baloxavir

    Laxatives containing polyvalent cations

    May decrease baloxavir concentrations and decrease efficacy

    Avoid concomitant administration with baloxavir marboxil

    Midazolam

    No effect on pharmacokinetics of midazolam

    Multivitamins

    May decrease baloxavir concentrations and decrease efficacy

    Avoid concomitant administration with baloxavir marboxil

    Oseltamivir

    No effect on pharmacokinetics of oseltamivir, baloxavir marboxil, or baloxavir

    Probenecid

    No effect on pharmacokinetics of baloxavir marboxil or baloxavir

    Rosuvastatin

    No effect on pharmacokinetics of rosuvastatin

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