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Medical information request
Medical information request

Medical information request

If you have any questions or concerns related to safety of siponimod, please contact Novartis Medical Information (MI) experts for evidence-based up-to-date information

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Using this webpage, you may also report an adverse event or product complaint

Report an adverse event

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* Indication varies in different countries. Current website is a global information resource. Local Prescribing Information/ Summary of Product Characteristics approved by individual country’s regulatory authority is the primary source of information for the indication of siponimod in the individual country.

The Pregnancy outcome Intensive Monitoring (PRIM) program is based on enhanced pharmacovigilance of the Novartis spontaneous reporting system. PRIM is an adverse event outcomes intensive monitoring program to collect information (targeted follow-up checklists) about pregnancy in patients exposed to siponimod immediately before or during pregnancy and infant outcomes 12 months after delivery.