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    Behçet

    ​Behcet’s (beh-CHETS) disease, also called Behcet’s syndrome, is a rare disorder that causes blood vessel inflammation throughout your body.
    The disease can lead to numerous signs and symptoms that may seem unrelated at first. They may include mouth sores, eye inflammation, skin rashes and lesions, and genital sores.
    The effects of Behcet’s disease vary from person to person and may clear up on their own.
    Treatment involves medications to reduce the signs and symptoms of Behcet’s disease and to prevent serious complications, such as blindness.

    Patient Advocacy groups

    No VPAGs for this SPECIFIC disease. See VPAGs covering ALL Vasculitis Diseases

    Are you a patient advocacy group ?

    respresenting patients with a primary form of vasculitis ?
    JOIN US !

    Centers of Expertise

    Erasmus MC

    Erasmus MC

    Are you a vasculitis expert centre ?

    dealing with one or more forms of a primary vasculitis
    JOIN US !

    News

    SVI Update Tavneos

    Update Tavneos® April 29th 2026

    29 april, 2026 Geen reacties

    The FDA has moved from a review to a formal proposal to withdraw approval of Tavneos in the United States.
    This is a more serious step than a review, but it is still not a final decision.
    In Europe, the EMA review is still ongoing. No conclusions have been reached yet, and Tavneos is still available.

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    FDA warning avacopan

    Update Tavneos Review – April 2026

    5 april, 2026 Geen reacties

    The U.S. Food and Drug Administration (FDA) issued a Drug Safety
    Communication on 31 March 2026, alerting healthcare professionals and patients to serious cases of drug-induced liver injury (DILI) in postmarketing surveillance of avacopan — including cases with fatal outcomes.
    While the FDA operates outside the European regulatory framework,
    its postmarketing findings are directly relevant to the EMA’s ongoing assessment.

    Read More »

    Rare Disease Day 2026

    28 februari, 2026 Geen reacties

    Rare Disease Day is marked every year on the last day of February. On this day, patients, families, healthcare professionals and organisations around the world come together to raise awareness about rare diseases and the people living with them.

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    Do it Now

    About us

    • We encourage and support Vasculitis Patient Advocacy Groups (VPAGs) to collaborate and grow stronger.
    • If there is no existing VPAG in a particular country we can  help to create one.
    • We collaborate with any institution willing to help us in achieving these goals.

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