Pharmacovigilance

Pharmacovigilance is a process associated with the detection, collection, evaluation, study and prevention of adverse reactions and any other issues related to the safety and effectiveness of medicinal products. In order to monitor the safety and effectiveness of medicinal products in their medical use, in accordance with the legislation of Ukraine, the applicant must create, ensure and guarantee the functioning of the FN system in Ukraine, which is a mandatory condition for the medicinal product to be in circulation in the territory of Ukraine.

The main priority of BIOTECHNOS is to provide the population with high-quality medicines. In order to make the treatment process more effective and safe, we need to maintain feedback from healthcare professionals, consumers and distributors.

Therefore, if as a result of taking our medicines, you have information about a side effect, the occurrence of an unexpected therapeutic effect, or the lack of effectiveness of the medicine, please report it to:

For communication 24/7  used:mailbox:  info@biotehnos.com.ua

Below is a message card form to fill out.

All fields are required to be filled out, if you do not know any information, you must indicate this in the appropriate field.

    Reporter information

    Full name*

    E-mail address*

    Status*

    Form submission date

    Contact phone number*

    Country, city*

    Healthcare worker information (if applicable)

    Patient information

    Patient's initials*

    Medical card number

    Sex*

    Age at the time of reaction*

    Contact details*

    Other important information (diagnoses, allergies, pregnancy, etc.)*

    Suspected drug

    Drug name*

    Primary diagnosis

    Release form

    Series

    Dose

    Multiplicity

    Method of administration

    Indications for appointment

    Start of treatment*

    End of treatment*

    What other medications were taken (trade name, dose, method, period)*

    Suspected adverse reaction

    Description of adverse event/lack of efficacy*

    Result of PQ/VE*

    Start date of the PY*

    End date of the PY

    Consequences

    Medications that were prescribed

    Means for correcting side effect/lack of effectiveness

    Cancellation of suspected drug
    YesNo

    Repeated prescription of drugs
    YesNo

    Was the cancellation accompanied by the disappearance of the PW?
    YesNo

    Did the PJ/VE recur after the dose change?
    YesNo

    Changing the dosage regimen

    Drug correction of PQ/VE

    The Law of Ukraine "On Personal Data Protection" establishes basic requirements for the collection, storage and processing of personal data. Informed consent of the patient involves the collection, transfer, use and storage of the patient's personal data.

    INFORMED CONSENT to the processing and transfer of personal data

    I consent to the processing of my personal data (i.e., the performance of actions related to the collection, registration, accumulation, storage, adaptation, modification, renewal, updating, use and dissemination (transfer), depersonalization and destruction, as well as the performance of other actions related to the processing of my personal data. The personal data provided by me may be distributed and transferred, including to healthcare institutions of foreign countries, state authorities and local self-government bodies, as well as to other persons determined by the owner/manager independently.
    I agree that such transfer of my personal data will not require separate consent or notification to me.