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CI OMS FORMDEBFARM16223897SUSPECT ADVERSE REACTION REPORT I. REACTION INFORMATION 1. PATIENT INITIALS1a. COUNTRYDEprivacy2. DATE OF BIRTH DA MO YR2a. AGE67 (Year)3. SEXFemale46 REACTION ONSET DA MO
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What is de-bfarm-16223897?
de-bfarm-16223897 is a form required by the German Federal Institute for Drugs and Medical Devices (BfArM) for the notification of medicinal products.
Who is required to file de-bfarm-16223897?
Manufacturers and distributors of medicinal products in Germany are required to file de-bfarm-16223897.
How to fill out de-bfarm-16223897?
de-bfarm-16223897 can be filled out electronically through the BfArM portal using the required information about the medicinal product.
What is the purpose of de-bfarm-16223897?
The purpose of de-bfarm-16223897 is to notify the BfArM of the availability of medicinal products in the German market.
What information must be reported on de-bfarm-16223897?
Information such as the name of the medicinal product, its marketing authorization number, the manufacturer's details, and the product's presentation must be reported on de-bfarm-16223897.
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