Alembic Pharmaceuticals Limited (Alembic) is focused for patient safety. To better understand safety profile of our product, we collect adverse events through various sources, evaluate and report them to the Agency.
An adverse event (AE) is any untoward medical occurrence in a patient administered a pharmaceutical product and which does not necessarily have a causal relationship with this treatment. An adverse event can therefore be any unfavourable and unintended sign, symptom, or disease associated with the use of the product.
Report an adverse event related to Alembic product