Pharmacovigilance

Safety information on Top-Pharma products

Report an adverse reaction or incident

Patient safety

Patient safety is important to us. Reporting adverse reactions, incidents and other safety concerns contributes to the continuous monitoring of our products and helps identify new information related to their use.

The role of pharmacovigilance

Pharmacovigilance contributes to monitoring the safety of medicinal products by identifying and preventing adverse reactions or other risks associated with their use.

You can always report

If you or someone close to you has experienced a suspected reaction after using a medicinal product, an undesirable effect associated with a food supplement, or an incident involving a medical device, you can submit a report even if you are not certain that the product was the cause.

Report an adverse reaction or incident

This form is intended for reporting adverse reactions and incidents and does not replace medical advice. If your condition worsens, seek medical attention immediately. In a medical emergency, call 112.

Please provide the information you know. You do not need all the details to report. Fields marked with * are required.

The product
Product type *
The reporter
I am reporting as *

Provide at least one contact method. *

The patient
Product use
The event
What happened, and what symptoms or consequences occurred?
Approximate date, if the exact date is unknown
Special situations
Additional information
PDF, JPG or PNG. Up to 3 files, 10 MB per file and 20 MB in total. Remove personal data that is not needed.

What happens after you report? Our team will review the information and may contact you for clarification. Relevant data will be shared with the marketing authorisation holder or manufacturer and the competent authority, as applicable.

Other ways to report

Pharmacovigilance contact

Reporting to AMDM

You may also report directly to the Medicines and Medical Devices Agency (AMDM).

AMDM reporting form
For partners

Pharmacovigilance and medical device vigilance

We provide local pharmacovigilance and medical device vigilance services for our partners in the Republic of Moldova, including the collection and assessment of safety information and communication with the competent authority.

Our system operates in compliance with Good Pharmacovigilance Practices (GVP) and applicable national and European requirements.

Our services include

  • Local Qualified Person for Pharmacovigilance with 24/7 availability
  • Management of adverse reaction reports and other safety information
  • Local literature and regulatory intelligence
  • Submissions and communication with local regulatory authorities
  • Support for PSURs, RMPs and risk minimisation measures
  • Preparation and support for pharmacovigilance audits and inspections