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CI OMS FORMDEBFARM17081680SUSPECT ADVERSE REACTION REPORT I. REACTION INFORMATION 1. PATIENT INITIALS1a. COUNTRYDEprivacy2. DATE OF BIRTH DA MO YR2a. AGE69 (Year)3. SEXFemale46 REACTION ONSET DA MO
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What is de-bfarm-17081680?
de-bfarm-17081680 is a form used for reporting certain pharmaceutical information to the Federal Institute for Drugs and Medical Devices (BfArM) in Germany.
Who is required to file de-bfarm-17081680?
Pharmaceutical companies and manufacturers are required to file de-bfarm-17081680.
How to fill out de-bfarm-17081680?
de-bfarm-17081680 can be filled out electronically through the BfArM's online portal or by submitting a physical copy via mail.
What is the purpose of de-bfarm-17081680?
The purpose of de-bfarm-17081680 is to provide the BfArM with information on pharmaceutical products, including sales data and adverse event reporting.
What information must be reported on de-bfarm-17081680?
Information such as product sales data, adverse events, product recalls, and any changes to product labeling must be reported on de-bfarm-17081680.
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