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Xofluza(Baloxavir marboxil)

Another Name速福达、LuciBal

IndicationsIt is indicated for the treatment of acute uncomplicated influenza in people aged 5 years and older, and for post-exposure prophylaxis of influenza.

  • Reg No.07 L 1394/25

  • Inspection No.1767-23

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    Dosage form:Tablets

    Specs:20mg*4 tablets/box

    Indate:96 months

    Warm tips:Please purchase and use the medication under pharmacist guidance as the outer packaging is for reference only and the information is intended for professionals.
    Introduction of Xofluza

    This prescription drug was approved by the FDA in the United States in 2018. It targets the cap-dependent endonuclease of influenza A and B viruses and must be used strictly under medical supervision.

    Instructions of Xofluza

    Target of Action

    Cap-dependent endonuclease of influenza A and B viruses

    Dosage and Administration

    Route and frequency of administration for Baloxavir marboxil (Xofluza): Oral, once daily.

    The dosage of Baloxavir marboxil (Xofluza) should be adjusted based on the patient's actual condition. For specific details, consult your doctor and follow medical advice.

    Recommended reading: Dosage and Administration of Baloxavir marboxil (Xofluza)

    Side Effects

    Common side effects: Diarrhea, bronchitis, nausea, etc.

    Serious side effects: Difficulty breathing, rash, urticaria or blisters, etc.

    Reference article: Side Effects of Baloxavir marboxil (Xofluza)

    Use in Special Populations

    Pregnancy: It is currently unknown whether Baloxavir marboxil (Xofluza) can harm your unborn baby.

    Breastfeeding: It is currently unknown whether Baloxavir marboxil (Xofluza) passes into your breast milk.

    Daily Precautions

    1. Baloxavir marboxil (Xofluza) may contain inactive ingredients that could cause allergic reactions or other problems.

    2. Follow all instructions on the drug label and package. Inform every healthcare provider of all your health conditions, allergies, and all medications you are using.

    FDA,2025.05

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