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Reporting of side effects after taking or using a Sobi product can be done directly to the Federal Agency for Medicines and Health Products via www.eenbijwerkingmelden.be (Dutch) or www.notifieruneffetindesirable.be (French) via [email protected]; in Luxemburg, to the Centre Régional de Pharmacovigilance de Nancy or the Direction de la Santé - Division de la Pharmacie et des Médicaments via www.guichet.lu/pharmacovigilance; alternatively to Sobi via email to [email protected].

The information on this website is intended for Healthcare Professionals only.
© 2023 Swedish Orphan Biovitrum AB (publ).

Date of last revision of site: August 2024
PP-21217

Swedish Orphan Biovitrum (Belgium) BV
Hermeslaan 11
1932 Zaventem
Belgium
Tel: +32 2 880 61 19
[email protected]

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