Adverse Reaction Reporting – Celon Pharma S.A.
In accordance with the legal requirements of the Pharmaceutical Law Act of 6 September 2001, Celon Pharma S.A., as the marketing authorization holder, is obliged to collect all information regarding the occurrence of adverse reactions resulting from the use of medicinal products for which it holds marketing authorization. Reporting adverse reactions helps gather more information about the safety of the medicine.
An adverse reaction is any harmful and unintended response to a medicinal product.
Reporting Instructions
• By phone: +48 22 751 59 33 (available during office hours, 8:00 AM – 4:00 PM).
• By form: Fill out the [ADVERSE DRUG REACTION REPORTING FORM] and send a scanned copy to: dzialania.niepozadane@celonpharma.com.
• Or mail the original to: Celon Pharma S.A., Ogrodowa 2A, 05-092 Łomianki / Kiełpin, with the note 'Adverse Reactions'.
You may also report using the online form below.
Fields marked with an asterisk (*) are mandatory.
In case of reporting information about the use of a drug by a pregnant woman, please download and complete the form: [EXPOSURE TO MEDICINAL PRODUCT DURING PREGNANCY FORM]