Adverse Events Reporting
Pharmacovigilance is an activity of shared responsibility between all agents related to medications or vaccines.
Adverse drug reactions (ADRs) are classified as serious and non-serious; even if they are headaches during or after the administration of a medication, they can be reported.
Special situations: overdose, medication error, misuse, abuse, non-prescription use, lack of efficacy, unintended benefit, suspected transmission of infectious agents and fetal exposure during pregnancy and/or lactation.
Medical Information and Pharmacovigilance:
Pharmacovigilance: PhvPanama@cslbehring.com
Medical information: Medical_glad@cslbehring.com
Product quality reports: Qualityglad@cslbehring.com
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