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Filgotinib(Jyseleca)

Another NameJyseleca、Fequintinib、LuciFilgo

IndicationsAdult patients with moderate to severe rheumatoid arthritis (RA) who have insufficient or intolerant response to various disease modifying antirheumatic drugs (DMARD).

  • Reg No.06 L 1112 /24

  • Inspection No.1072-24

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    Dosage form:Tablet

    Specs:100mg*30 tablets

    Indate:24 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 Filgotinib

    Filgotinib is a prescription drug targeting Janus kinase 1 (JAK1). It was first approved for marketing in the European Union and Japan in September 2020. It should be used strictly under medical supervision.


    Instructions of Filgotinib

    Target of Action

    Janus kinase 1 (JAK1)

    Dosage and Administration

    Route and frequency of administration for filgotinib: Oral, once daily.

    The dosage of filgotinib should be adjusted according to the patient's actual condition. For specific adjustments, consult a physician and follow medical advice.

    Recommended reading: Dosage and Administration of Filgotinib

    Side Effects

    Common side effects: Nausea, upper respiratory tract infections, etc.

    Serious side effects: Serious infections (e.g., pneumonia), herpes zoster, etc.

    Reference article: Side Effects of Filgotinib

    Use in Special Populations

    Pregnancy: Filgotinib is contraindicated in pregnant patients.

    Lactation: It is unknown whether this drug is excreted into human milk. Breastfeeding women should not use filgotinib.

    Daily Precautions

    1. Before treatment, a comprehensive evaluation by a specialist is mandatory, with strict screening for contraindications and close monitoring during therapy.

    2. Filgotinib is primarily metabolized by the CES2 enzyme. Caution is required when co-administered with CES2 inhibitors (e.g., simvastatin).

    3. During treatment and for a period before and after, live vaccines are prohibited.

    from FDA,2023.07

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