Medwatch is a way of reporting adverse effects of a medication?

A. Determining which medication needs a prescription for the patient to obtain. The DEA does not determine which medications require prescriptions; this is typically under the jurisdiction of the Food and Drug Administration (FDA).

B. Ensuring the patient taking a medication has an option for generic medications. This role is more aligned with the FDA, which oversees the approval of generic medications. The DEA does not handle generic medication options.

C. Providing specific requirements for the manufacture of generic medications. This is also a role of the FDA, not the DEA. The DEA focuses on controlled substances, not the specifics of generic drug manufacturing.

D. Indicating which medications are controlled substances and enforcing the laws. This accurately describes the role of the DEA. The DEA classifies controlled substances into schedules and enforces the laws related to the handling, prescribing, and dispensing of these drugs.

A. A medication that supports physiological well-being: A placebo does not have active therapeutic effects and is used in research, not for direct physiological support.

B. Medication designed to have more benefits than risks: This statement refers to a drug with a favorable benefit-risk profile, not a placebo.

C. An inactive substance that is used for comparison in drug studies: This is the correct definition of a placebo. It is an inactive substance that has no therapeutic effect, used to compare against the active drug in clinical trials.

D. The active ingredient in a drug preparation: This statement describes the component responsible for the therapeutic effect of a drug, not a placebo.