The goals of pharmacovigilance are:

• Continuous assessment of the benefit-risk ratio throughout the entire period of circulation of medicines and medical devices;

• Ensuring the protection of public health and improving patient safety;

• Raising the awareness of healthcare and pharmaceutical professionals about drug safety, the rational use of medicines and increasing their activity in monitoring the side effects of medicines.

Pharmacovigilance system is designed to perform pharmacovigilance tasks and responsibilities, to monitor the safety of medicines and medical devices, to detect all changes in the assessment of the benefit-risk ratio of medicines in a timely manner, to develop and implement measures to ensure the use of medicines in excess of the benefits over the risks.

"DOSFARM" LLP has established and maintains a system to ensure that all suspected adverse reactions are collected (reported to company personnel and/or medical representatives) and that the information received is promptly transmitted to the authorized body.

The pharmacovigilance system at "DOSFARM" LLP is located at: 3 Chaplygin street, Zhetysu district,
Almaty city, 050034, Republic of Kazakhstan

The Qualified Person Responsible for Pharmacovigilance is:

Name - Balpanova Nurila Daurenkyzy

tel.: +7 (727) 364 84 27

fax: +7 (727) 253 03 88

Mobile: +7 747 843 56 57

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The person substituting the Qualified Person Responsible for Pharmacovigilance is:

Name - Shigayeva Irina Anatolyevna

tel.: + 7 (727) 364 84 27

fax: +7 (727) 253 03 88

Mobile: +7 701 403 74 50

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If you have any information about an occurred (suspected) adverse reaction or lack of effectiveness when using medicines manufactured by "DOSFARM" LLP, we kindly ask you to inform us about it by the above-mentioned phone numbers and e-mail.

We guarantee the confidentiality of information sent by you, except as required by law.