Side effects

Here you can report the adverse drug effect of a medicinal product

 

Tarchomińskie Zakłady Farmaceutyczne ‘Polfa’ Spółka Akcyjna is obliged by the Pharmaceutical Law to collect, register and monitor all adverse reactions related to its own medicinal products, reported by medical practitioners and patients or their carers.

An adverse drug reaction (ADR) is an unwanted or harmful reaction experienced following the administration of a drug or combination of drugs under normal conditions of use and is suspected to be related to the drug.

We kindly ask you to report to us any observed adverse reaction and any other information regarding the use of our medicinal products through one of the following options:

• by a phone number: +48 (22) 811 18 14
• by an e-mail address: pharmacovigilance@polfa-tarchomin.com.pl

1. Download the form:

• I am a patient / patient carer
• I am a medical practitioner

2. Fill it up
3. Send to pharmacovigilance@polfa-tarchomin.com.pl

• by post or fax:

1. Download the form

• I am a patient / patient carer
• I am a medical practitioner

2. Print and fill it up
3. Send to the address:

Tarchomińskie Zakłady Farmaceutyczne “Polfa” S.A.

Dział Bezpieczeństwa Farmakoterapii

A. Fleminga 2, 03-176 Warszawa

4. Or send it by fax to: +48 (22) 510 90 25

We kindly ask You to provide the most detailed description of the adverse reaction. Any information can be extremely valuable in establishing a causal relationship between a drug and an adverse reaction.

Please also inform us about cases of using our medicines during pregnancy, breastfeeding and other reports related to the safety of our products.

By reporting side effects, you can help gather information on a particular medicine, and thus increase its safety.

ATTENTION: The contact forms provided are not intended to provide medical advice and consultations (in the case of currently worrying symptoms, in the first place, please contact your doctor or other healthcare professional).