Pursuant to the Act of 6 September 2001 Pharmaceutical Law, Temapharm Sp. z o.o. is obliged to keep a register of all adverse events connected with its own medicinal products reported by health professionals (medical doctors, dentists, pharmacists, medical assistants, laboratory diagnosticians, paramedics, pharmaceutical technicians) as well patients and their carers.

Adverse events – any undesirable or unintended effect of a medicinal product.

If you are a patient or a carer of the patient who has experienced any undesirable effect resulting from the use of any of Temapharm Sp. z o.o. products or if you are a doctor/ pharmacist/ health care employee and would like to report any undesirable effect that occured in your patient during the application of our medicinal product, please inform us about the incident by filling in the adverse event form below. The reported incident will be investigated by and our company's represensttive will contact you in order to get additional information.

Last modified on : 2014-01-22

Contact details for Adverse Drug Reaction reporting:


Pursuant to the provisions of Law 15/1999 of December 13, Protection of Personal Data (LOPD), Exeltis informs you that the personal data provided by you will be included in the PHARMACOVIGILANCE file, of which the company is responsible. These personal data are collected and stored in order to comply with legal requirements on reporting adverse drug reactions and for the evaluation of their benefit-risk balance. You can exercise your rights of access, rectification, cancellation and opposition to the processing of the data through written communication to the following address: Nectar Building. Quintanapalla, 2 4th floor 28050 Madrid, Spain.