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CI OMS FORMDEBFARM17099573SUSPECT ADVERSE REACTION REPORT I. REACTION INFORMATION 1. PATIENT INITIALS1a. COUNTRYDEprivacy2. DATE OF BIRTH DAMO2a. AGE3. SEXYR46 REACTION ONSET DAMOYRFemale7. + 13.
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What is de-bfarm-17099573?
de-bfarm-17099573 is a specific form or report required by the German Federal Institute for Drugs and Medical Devices (BfArM).
Who is required to file de-bfarm-17099573?
Manufacturers, distributors, or entities involved in the pharmaceutical industry may be required to file de-bfarm-17099573.
How to fill out de-bfarm-17099573?
de-bfarm-17099573 should be filled out according to the guidelines provided by BfArM, including providing detailed information about pharmaceutical products.
What is the purpose of de-bfarm-17099573?
The purpose of de-bfarm-17099573 is to ensure compliance with regulatory requirements and to monitor the safety and effectiveness of pharmaceutical products.
What information must be reported on de-bfarm-17099573?
Information such as product details, manufacturing processes, distribution channels, and adverse events may need to be reported on de-bfarm-17099573.
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