You may report an adverse event by telephone at +49 6131 90840 or use the following web form.

Adverse events that occur as part of a clinical trial must be reported to the appropriate coordinating study center.

If you are suffering, or the person on whose behalf you are reporting is currently suffering from a serious adverse event, you should contact your physician or other healthcare professional before reporting the adverse event.

The products listed here may have different methods of approval depending on country.

Do you have a medical inquiry regarding our COVID-19 mRNA vaccine (BNT162)? In that case, please use this website ( and choose your relevant country.

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