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CHEPLAPHARM Arzneimittel GmbH

Drug Safety

Adverse Drug Event Reporting are important information for monitoring the safety of our medicines and taking appropriate action when needed.

In case you want to report a suspected case of Adverse Drug Event, kindly fill out the form available here as completely as possible and send it to: drugsafety(at)

You can also reach our Drug Safety department by phone or fax at:
Tel.: +49 (0) 3834 3914 329
Fax: +49 (0) 3834 3914 349
E-Mail: medinfo(at)

With regards to drug safety, we are interested in all reports that are associated with our products, irrespective of the severity of the Adverse Drug Reaction and whether or not the Adverse Reaction is already specified in the Summary of Product Characteristics (SPC) / Package Leaflet (PL).

Your message/report will then be assessed and collected in our database. Due to the legal requirements, we are obliged to pass on the Adverse Drug Reaction Reports to the appropriate authorities within specified timelines.

In case of medical emergencies, patients should immediately consult their doctor and/or emergency medical services.

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