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Division of Child and Family Services Family Programs Office: Statewide Policy Manual MTL 0209-12282011 Section 0209 Subject: Psychiatric Care Treatment Medication Administration Informed Consent
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What is medication administration informed consent?
Medication administration informed consent is a process where a patient or their legal representative gives permission for healthcare providers to administer medication and agrees to the potential risks and benefits associated with the medication.
Who is required to file medication administration informed consent?
The patient or their legal representative is required to file medication administration informed consent.
How to fill out medication administration informed consent?
To fill out medication administration informed consent, the patient or their legal representative must read and understand the information provided about the medication, discuss any concerns with the healthcare provider, and sign the consent form.
What is the purpose of medication administration informed consent?
The purpose of medication administration informed consent is to ensure that patients have a clear understanding of the medication they are receiving, its potential risks and benefits, and to ensure their consent is obtained before the medication is administered.
What information must be reported on medication administration informed consent?
Medication administration informed consent must include information about the medication being administered, its intended purpose, potential side effects or risks, alternative treatments, and the patient's agreement to receive the medication.
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