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CI OMS FORMDEBFARM17107691SUSPECT ADVERSE REACTION REPORT I. REACTION INFORMATION 1. PATIENT INITIALS1a. COUNTRYDEprivacy2. DATE OF BIRTH DA MO YR2a. AGE44 (Year)3. SEX46 REACTION ONSET DA MO YRFemale7.
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What is de-bfarm-17107691?
de-bfarm-17107691 is a form used for reporting information related to pharmaceutical products.
Who is required to file de-bfarm-17107691?
Manufacturers and distributors of pharmaceutical products are required to file de-bfarm-17107691.
How to fill out de-bfarm-17107691?
de-bfarm-17107691 can be filled out electronically or on paper, following the instructions provided by the regulatory agency.
What is the purpose of de-bfarm-17107691?
The purpose of de-bfarm-17107691 is to ensure transparency in the pharmaceutical industry and to monitor the safety and effectiveness of pharmaceutical products.
What information must be reported on de-bfarm-17107691?
Information such as product name, manufacturer, batch number, expiration date, and adverse reactions must be reported on de-bfarm-17107691.
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