Patient safety is a top priority for ELME MESSER GAAS.

In order to ensure control over the safety and effectiveness of medicines, the company operates a system of pharmacovigilance in accordance with current legislation, international standards and ethical principles of the company.
If you wish to report an adverse reaction and / or ineffectiveness in the medical use of medicines manufactured by our company (Messer liquid oxygen, Medical gaseous oxygen), please inform the Authorized Person responsible for pharmacovigilance in a way convenient for you.

Importantly! The message must contain information:

  • From whom the information came.
  • Who is the patient (name, gender, age).
  • Product that caused an adverse reaction or lack of efficacy (name of the drug, manufacturer, № series).
  • Detailed description of the adverse reaction or lack of efficacy.
  • Information about the doctor.
  • Contact for feedback.

Or contact us using the feedback for






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    The authorized person is responsible for pharmacovigilance
    Marianna Iaremenko
    E-mail: marianna.iaremenko@elmemesser.ua
    Mob.: +38 067 539 51 17 (around the clock)
    SC “MESSER UKRAINE”

    The authorized person is responsible for pharmacovigilance
    Halyna Verhunova
    E-mail: halyna.verhunova@elmemesser.ua
    Mob.: +38 067 573 65 33 (around the clock)
    PJSC “KHARKIV AUTOGENIC PLANT”

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