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CI OMS FORMDEBFARM17318172SUSPECT ADVERSE REACTION REPORT I. REACTION INFORMATION 1. PATIENT INITIALS1a. COUNTRYDEprivacy2. DATE OF BIRTH DA MO YR2a. AGE3. SEX51 (Year)Male46 REACTION ONSET DA MO
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What is de-bfarm-17318172?
de-bfarm-17318172 is a form used for reporting information related to pharmaceutical products in Germany.
Who is required to file de-bfarm-17318172?
Manufacturers, distributors, and sellers of pharmaceutical products in Germany are required to file de-bfarm-17318172.
How to fill out de-bfarm-17318172?
de-bfarm-17318172 can be filled out online through the official website of the German Federal Institute for Drugs and Medical Devices.
What is the purpose of de-bfarm-17318172?
The purpose of de-bfarm-17318172 is to ensure transparency and compliance in the pharmaceutical industry in Germany.
What information must be reported on de-bfarm-17318172?
Information such as product name, manufacturer details, marketing authorization number, and sales data must be reported on de-bfarm-17318172.
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