Radiopharmaceuticals

Reporting of Adverse Reactions

 

This is the obligation of Marketing Authorization Holder to assure that any aspect which could impact the safety profile of authorized medicinal products is detected and assessed and that necessary measures are taken. This monitoring is called pharmacovigilance and requires collecting and managing data on the safety of medicines, especially information about Adverse reactions caused by the medicinal product.

 

If you want to report Adverse reaction of Synektik SA or Synektik Pharma Sp. z o.o. medicinal product, please use the following:

phone: +48 22 327 09 40 (24h voicemail)
e-mail: phv@synektik.com.pl

 

For more information on Pharmacovigilance please see the website of Office for Registration of Medicinal Products, Medical Devices and Biocidal Products (link to the website).