Adverse Event Reporting


Home / Adverse Event Reporting

Pharmacovigilance Department – Adverse Event Reporting

In case you need to report an adverse event related to Specifar’s medicinal products, please contact the Pharmacovigilance Department:

Telephone 1: +30 211 880 51 66 (Office Hours)
Telephone 2: +30 6940 27 24 68 (24 Hours)
Fax 1: +30 211 880 51 07 (24 hours)

Or please fill the following formula:

* The information you provide in this form will be recorded by SPECIFAR S.A. as part of its legal obligations related to our products and will be protected and handled confidentially and in line with applicable data protection laws and TEVA’s Privacy Policy. This information may be shared with other Teva entities and certain authorities to be evaluated and collated with other events (including quality) recorded about that product or active ingredient, in order to assess the benefit – risk balance of the medicines you have used and if needed to update the product information and for the purposes of attending to your request. The information you provide today may be stored outside the EU. If you do not agree to these uses of your information and wish to object to this processing or wish to access, rectify or delete your personal information please email We also inform you that you have the right to data portability and the right to obtain from SPECIFAR S.A. restriction of processing. Moreover, you have the right to lodge a complaint with a supervisory authority. Further information can be found in a more detailed notice here. If you are not the subject of this report, please ensure that individual who is the subject of the report is aware of this submission, including the possible transmission of his/her personal information.