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What is an
Adverse Event (AE)?
Any undesirable medical condition (illness, symptom, sign, or abnormal laboratory result) that occurs in a patient and is temporally associated with the use of a pharmaceutical product, whether or not it has a causal relationship with the product.
Laboratorios Bagó S.A. is committed to providing maximum efficacy and reliability by enhancing benefits and minimizing potential risks. This involves continuous monitoring of the safety of our products during both their development phase and their commercialization or extended use.
To report an adverse event or for any concerns regarding the safety of our medicines, both patients/consumers and healthcare professionals can contact us through the following channels: