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Adverse Event Reporting

At Martin Dow Marker Ltd., Medical Affairs play an integral role in Pharmacovigilance. Often known as drug safety, pharmacological science is the collection, detection, assessment, monitoring, and prevention of Adverse Events with pharmaceutical products. We provide a productive flow of operations in Medical Affairs by handling medication safety, examining individual adverse event reports, and promptly reporting any adverse events involving medicinal products. As a result, ethical practice and a patient-centered workflow are maintained.

What Is an Adverse Event?

An adverse event (AE) is any undesirable (unwanted) medical occurrence in a patient, who has been given a pharmaceutical product that does not necessarily have a causal relationship with his treatment.

An adverse effect is considered as any unfavorable and unintended sign, symptom, or disease associated with the usage of the product.

Why Report Adverse Events?

Patient safety is paramount to us at Martin Dow Marker Ltd. Your reports help us in safeguarding our patients, our products and fulfill the responsibilities of reporting information on adverse effects to the relevant health authorities.

Adverse Event Reporting

Reaction Information

Check appropriate:

Suspected drug information:

Did the adverse reaction stop after stopping the drug?

Did the reaction reappear after reintroduction stop after stopping the drug?

Concomitant drugs and history

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For Adverse Events and Medical Information Queries,
have queries?

Connect With Us

For information and queries:

+92 21 111 111 634

For information and queries:

+92 21 350 605 41

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