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Description
Patients require evaluation before starting DMARDs to rule out contraindications to the medications (meaning the patient should not take a certain medication due to the harm it would cause) and monitoring while using them to watch for serious side effects
Congress intended for the FDA to refer to a substantive body of evidence about the safety and effectiveness of ingredients put on the bulks list, she said

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To be used by trained professionals only
Drug compounding defined by the FDA as the process of combining, mixing or altering ingredients of a drug to create a medication tailored to a patients needs was the primary way drugs were produced until large-scale pharmaceutical manufacturing emerged early in the 20th century
