Services

Pharmacovigilance


Pharmacovigilance (PV) is defined as the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other drug-related problem.
 
Adverse drug reaction is a response to a drug which is noxious and unintended, and which occurs at doses normally used in man for the prophylaxis, diagnosis, or therapy of disease, or for the modifications of physiological function.
 
Being responsible for drug and patient safety, company "Briz" has created a system of pharmacovigilance and continues to develop drug safety monitoring.
 
If you use our medicine or treat patient with our medicine and notice any side effect, we ask you to report to the Pharmacovigilance department:
- By filling in the electronic reporting form
- write to E-mail: adr@briz.lv
- By phone: +371 67259281 (24-hour access phone)

Due to the European Parliament General Data protection regule (GDPR), which entered into force on May 25, 2018, when filling out an application, you have agreed to appropriate data processing aimed at controlling the side effects. SIA BRIZ does not process or store data more than it is necessary in accordance with the company's data processing and protection policy.
 
Task of Pharmacovigilance department is in a timely manner to prevent potential risks to the patient, as well as to discover hitherto unknown effects, both positive and negative.
 
You can help us to get a lot more information about the safety of medicines by reporting of adverse reactions.
 
Please also report on the ineffectiveness of the medicine, other unusual effects, as well as inappropriate drug use cases.
 
You can also contact us in case you have any questions about the use of our medicines.
 
We guarantee full confidentiality of your data!
Doctor application
Patient application

Healthcare professional report on adverse drug reactions

Information on the person who submitted report

To clarify (if necessary) the information referred to in the report, please provide phone number and / or e-mail address.

Information about the patient

Please indicate the full number of years or months
Please indicate the exact weight in kilograms
Please state, if the patient is hospitalised

Adverse drug reaction (ADR) description











Suspected drug which might cause adverse drug reaction

** Indicate the name brand of the product; the active substances - see details on the packaging of medical products.
+ Add more

Concomitant drugs used in last 3 months (including self-treatment)

+ Add more

Additional information

Electronic Patient Report Form

Information on the person who submitted report

To clarify (if necessary) the information referred to in the report, please provide phone number and / or e-mail address.

Information on the person who submitted report






(fill in if permitted to contact your doctor as set out in section 6; if no permission granted- enter your initials)
Please indicate the full number of years or months
Please indicate the exact weight in kilograms
If the patient hospitalised - indicate the hospital





Adverse drug reaction (ADR) description

Please describe Adverse Drug Reaction/s, providing the most useful information
(If continued less than 24 hours, specify hours)

Known information













Suspected drug which might cause adverse drug reaction

+ Add more

Concomitant drugs used in last 3 months (including self-treatment)

+ Add more

Information about patient's doctor