Drug Side Effect

Dear Sir or Madam,
Pursuant to the legal requirements of the Pharmaceutical Law Act of September 6, 2001, Polpharma, as the Marketing Authorization Holder, is obliged to collect all information about side effects resulting from the use of the company's products as part of its supervision over the safety of therapy. These activities are carried out in order to minimize the side effects of the therapy and, thus, improve the safety of the patient's use of drugs.

A side effect is an unintended and unwanted reaction to a medicine.

In the event of any side effect after the use of a POLPHARMA or POLFA WARSAW product, the side effect may be reported to the Pharmacovigilance and Medical Information Department:

Pharmacovigilance and Medical Information Department
Zakłady Farmaceutyczne POLPHARMA S.A.
6 Bobrowiecka Street,
00-728 Warsaw,
e-mail: phv@polpharma.com
fax: +48 22 364 61 66
phone: +48 22 364 61 00

It is possible to report a side effect using an electronic form, which will be sent to the Pharmacovigilance and Medical Information Department of the POLPHARMA Group for further processing.
The application will be analyzed by us; in the case of additional questions, a representative of the company will contact you for additional information.

For this purpose, please complete the MEDICINE SIDE EFFECT REPORTING FORM.

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