Report adverse events
THIS SITE IS NOT INTENDED OR DESIGNED FOR REPORTING OF ADVERSE EVENTS
ViroGates is required to document reports of adverse events, both for comprehensive safety monitoring of its products and also to fulfill reporting requirements to Regulatory Authorities. It allows continued monitoring of the benefit/risk balance of the medicinal product.
Adverse events should be reported. Reporting forms and information can be found at fda.gov or through the FDA Adverse Event Reporting System (FAERS). Adverse events should also be reported to ViroGates A/S. Please contact ViroGates Adverse Events by emailing firstname.lastname@example.org or calling +45 2113 1336.
Please provide the brand name and batch number, where possible. It is very important that safety surveillance is carried out on a brand/product specific basis to ensure the information collected is accurate.
Date of preparation: January 2021