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STATE OF WISCONSIN 42 CFR483.420(a)(2) DHS 134.31(3)(o) DHS 94.03 & 94.09 s.51.61(1)(g) & (h) DEPARTMENT OF HEALTH SERVICES Division of Mental Health and Substance Abuse Services F24277 (12/2010)

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What is informed consent for medication?

Informed consent for medication is the process by which a healthcare provider explains the risks, benefits, and alternatives of a medication to a patient before the patient agrees to take the medication.

Who is required to file informed consent for medication?

Healthcare providers are required to file informed consent for medication with their patients.

How to fill out informed consent for medication?

Informed consent for medication can be filled out by providing the necessary information to the patient and obtaining their signature or consent.

What is the purpose of informed consent for medication?

The purpose of informed consent for medication is to ensure that patients are fully informed about the medication they are taking and have given their voluntary consent.

What information must be reported on informed consent for medication?

Information such as the name of the medication, potential side effects, dosage instructions, and alternative treatment options must be reported on informed consent for medication.

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