For Doctors and Healthcare Professionals

NovaMedica is a new kind of pharmaceutical company. Our strategy is to search the world for important new approved products that will help improve the health care of Russians, in addition to the exciting line of pipeline products we will in-license from the portfolio companies of Domain Associates in which our shareholders choose to invest. We will bring these products to Russia and the CIS countries and then market them to Russian/CIS specialty physicians and health care providers better than anyone else. As part of our mission to be a leading provider in Russia and the CIS of innovative specialty pharma products and solutions that treat a range of therapeutic disorders, we will be developing this site over the coming months to provide Russian and CIS healthcare professionals with an assortment of educational and information resources.

NovaMedica’s priority is the safety and effectiveness of its pharmaceutical products. Collection of information in this area allows us to receive the most complete and accurate data on the products and provide it to patients and doctors.

Effectiveness and safety of pharmaceutical products are monitored and studied continuously throughout all stages of the drug’s existence: during development, pre-clinical and clinical trials and for the entire time that it is available in the market. According to Federal Law 61-FZ dd April 12, 2010 on Circulation of Medicines registered products circulating in the territory of the Russian Federation are subject to the effectiveness and safety monitoring for the purpose of detecting any possible adverse effects of their use, warning healthcare professionals and patients and protecting patients from the consequences of using such products.

In line with its ethical principles and in compliance with the requirements of the Russian law, NovaMedica, as holder of or authorized person under marketing authorizations, ensures collection, registration, processing, analysis and storage of messages received in relation to safety of pharmaceutical products. You can send us any information on adverse reactions, drug interactions, idiosyncrasies, as well as any other facts or circumstances posing a threat to human life or health or changing the relation between the expected benefit and the possible risk of using the products in accordance with the international safety standards.

Please inform us of any side effects or other adverse events that your patients might have experienced as a result of using our company’s pharmaceutical products.​

The information that you submit will help make our products more effective and safe. By collecting safety information our company can receive and provide to patients and doctors the most complete and accurate data on the products’ safety profiles and detect rare side effects, which, in its turn, helps the doctors prescribing the products to correctly assess their safety and better control the patients’ treatment.

If you learned some information about a product, send it to us even if you are not sure that this information is significant.

What should be reported and how?

If you learned any information related to safety of NovaMedica’s products, including information on adverse reactions, complaints regarding quality, lack of therapeutic effect, etc., please send us a detailed message as soon as possible (ideally within 24 hours) using any of the channels listed below:

1. call the pharmacovigilance hotline: 8 (800) 222-49-08;

2. send a message in free format by mail to our address: 8, 2^nd Brestskaya St., 125196 Moscow, Russia, Panorama Business Center, 15^th floor, office of NovaMedica LLC (marked “Pharmacovigilance” or “Information on pharmacosafety”);

3. send a message in free format by E-mail to ;

4. download the proposed safety alert form (follow the link), fill it out and send it by mail to the address specified in i. 2 or by E-mail to  ;

5. fill out the online safety alert form.

By sending a message to NovaMedica you confirm that you Consent to processing of your personal data (for the text of the consent, follow the link), as well as any information contained in the message.

Please ensure that you have provided the minimum required information in your message:

• Patient or consumer of the product (initials / gender / age). NB: personal data of the patient or consumer of the product is not to be specified.
• Suspected drug (even if the casual relationship is doubtful);
• Description of the adverse drug reaction or other safety information (date of the incident, word-for-word description of the events);
• Original source (the person that provided the information and his/her contact details). You can provide the name or initials, address or qualifications (e.g., doctor, pharmacist, etc.); contact details are required for feedback (phone number, postal address, E-mail);
• Date on which you received the information.