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DALHIMPHARM JSC puts patient health care first. We collect, analyze and immediately respond to any information related to the safety and effectiveness of medicines manufactured by our Company.
If you have become aware of any adverse events* resulting from the use of a drug manufactured by DALHIMPHARM JSC, please fill out the electronic notification form. Your message will be processed as soon as possible by our specialists.
* What is an "undesirable phenomenon"? |
"adverse event" is any adverse change in the state of health of a patient or a clinical trial subject who has been prescribed a medicinal (investigational) drug, regardless of the causal relationship with its use. An undesirable phenomenon can be any unfavorable and unintended change (including a deviation of a laboratory indicator from the norm), a symptom or a disease, the time of occurrence of which does not exclude a causal relationship with the use of of the medicinal product, regardless of the presence or absence of a relationship with the use of the medicinal product.
Form for submitting information to the pharmacovigilance service