Adverse event reporting
Kowa routinely monitors the safety of all its medicines. This includes review of safety data from clinical studies, and collection of reports and cases of adverse events for marketed products.
Patients and Volunteers in clinical trials reporting an adverse event must contact the investigator.
For specific medical information requests please contact the partner responsible for distribution in your country.
For reporting adverse events within Europe Union please contact local distributor or Recordati
- +39 02 487871
For reporting adverse events within Middle East and North Africa (MENA) please contact…
- +961 9 222 050 ext 286