At Saba İlaç Sanayii ve Ticaret A.Ş., monitoring the safety of our products and protecting patient safety are among our priorities.

Reporting possible adverse events associated with the use of medicinal products is important for the evaluation of drug safety and the implementation of necessary measures.

You may report any side effect (adverse reaction) that you believe may have occurred during the use of Saba İlaç products.

Adverse event reports may be submitted by healthcare professionals, patients, or patient relatives.

How to Report an Adverse Event?

You may submit your adverse event / adverse reaction reports related to Saba İlaç Sanayii ve Ticaret A.Ş. products through one of the following methods:

1. Reporting via the TUFAM Adverse Event Reporting Form

You may submit your adverse event report using the TUFAM Adverse Event Reporting Form prepared by the Turkish Medicines and Medical Devices Agency (TİTCK).

📄 Click here to download the TUFAM Adverse Event Reporting Form.

After completing the form, you may send it to the following e-mail address:

✉ E-mail: [email protected]

2. Reporting by Phone

You may also submit your adverse event report by phone.

📞 Phone: +90 212 692 92 92

To make a report by phone, please press 5 during the call to reach the pharmacovigilance unit.

About Pharmacovigilance

Pharmacovigilance covers activities related to the detection, assessment, understanding, and prevention of adverse reactions and other medicine-related safety issues that may arise from the use of medicinal products.

Saba İlaç Sanayii ve Ticaret A.Ş. carries out the necessary processes for monitoring and evaluating drug safety within the scope of applicable pharmacovigilance regulations and cooperates with relevant health authorities.

Adverse event reports are an important source of information contributing to the continuous monitoring of drug safety.

Personal Data Protection Notice

Information shared within the scope of adverse event reporting is processed in accordance with the Law on the Protection of Personal Data No. 6698 (KVKK) and the relevant legislation.

Personal data submitted during an adverse event report may be processed for the following purposes:

  • Monitoring the safety of medicinal products

  • Evaluating adverse reactions

  • Fulfilling pharmacovigilance obligations

  • Reporting to competent health authorities

The information shared within this scope may be transferred to the Turkish Medicines and Medical Devices Agency (TİTCK) and, where required, to other relevant competent health authorities in accordance with legal requirements.

Personal data are processed solely for the purpose of carrying out pharmacovigilance activities, and the necessary technical and administrative measures are taken to ensure data security.

Within the scope of KVKK, data subjects may submit their requests regarding the processing of their personal data to [email protected]