Adverse events of the medicinal product
Reporting an adverse reaction to a medicinal product
After hospitalization/medical visit, the patient, their legal representative, or actual guardian has the right to report any actions that seem inappropriate while taking a given medicinal product. These include both harmful actions and those that cause discomfort.
Applications can be submitted via:
- telephone contact with the place of previous care or during a visit to the hospital clinic. The professional staff of the unit receiving the report is responsible for further processing.
- electronic form for the patient https://smz2.ezdrowie.gov.pl
- the attached form, which after completion can be sent via e-mail to: ndl@urpl.gov.pl or send it printed and signed by post to the following address: Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, Department of Monitoring Adverse Effects of Medicinal Products, Al. Jerozolimskie 181C, 02-222 Warsaw.