Vorwarts Pharma
Pharmacovigilance
Pharmacovigilance is the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other medicine-related problem.

Timely identification of adverse reactions enables a comprehensive assessment of the benefit-risk balance of medicinal products and supports the development and implementation of measures to enhance their safety.

To ensure proper monitoring of the safety and efficacy of medicinal products, the marketing authorization holder must establish, maintain, and ensure the effective operation of a pharmacovigilance system within the company. This is a mandatory requirement for the circulation of medicinal products in Ukraine and is carried out in accordance with international pharmacovigilance standards and applicable national legislation, including the Procedure for Pharmacovigilance, approved by Order of the Ministry of Health of Ukraine No. 898 dated 26.12.2006, as amended by Order No. 996 dated 26.09.2016.
It is important to report the following:
  • adverse reactions during medical use of the medicinal product;
  • lack of effectiveness;
  • off-label use of the medicinal product;
  • overdose;
  • interaction with other medicinal products;
  • abuse and/or misuse of the medicinal product;
  • use during pregnancy and/or breastfeeding;
  • unexpected therapeutic effect;
  • errors in prescribing and/or taking the medicinal product;
  • adverse effects of the medicinal product during professional activities;
  • transmission of an infectious agent through the medicinal product.

If you experience any adverse reactions, lack of effectiveness, or other undesirable effects while using VORWARTS PHARMA medicinal products, please report them to us using any method convenient for you.

  • Fill out the relevant reporting form below.
  • Contact us by phone or email:
📞 24/7 hotline:
You may also report all suspected adverse reactions and/or lack of efficacy of any medicinal product to the State Expert Centre of the Ministry of Health of Ukraine via the Automated Pharmacovigilance Information System at the following link: https://aisf.dec.gov.ua.

All information provided is strictly confidential and will not be disclosed, except as required by law.
Adverse Reaction Reporting Form
Information about the patient
Information about the suspected medicinal product
Description of the manifestations of adverse reaction/lack of effectiveness
Information about the reporter
Information about the doctor and healthcare facility
*fields are required

Thank you for your trust and cooperation!

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