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PHARMACY SERVICES TABLE OF CONTENTS. . . . . . . . . . . . . .BENEFIT PHARMACY. . . . . . . . . .SERVICES. . . . . . . . . . .TELEPHONE. . . . . . . . . . . . . . CONTACTS. . . . . . . . . . . . .
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Non-FDA-approved refers to products or treatments that have not been approved by the Food and Drug Administration for use.
Healthcare providers or manufacturers are required to file non-FDA-approved products or treatments.
To fill out a non-FDA-approved form, providers must accurately document the product or treatment and its potential risks.
The purpose of reporting non-FDA-approved products is to ensure transparency and informed decision-making for patients.
The report must include details about the non-FDA-approved product, the patient receiving it, any adverse reactions, and the provider administering it.
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