Dhs 1643-2025

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Informed consent is the process in which a health care provider educates a patient about the risks, benefits, and alternatives of a treatment. The patient must be competent to make a voluntary decision about the treatment. Written informed consent is required for the use of psychotropic medications.
A valid informed consent must satisfy three elements: type and amount of information provided to the patient, voluntariness of the patients decision-making, and the patients competence to make the requisite decisions.
Because they affect the brain and mind, anti-dementia medication and opioids can be classed as psychotropic medication. When more than one psychotropic agent is used, especially in the elderly, the side effects and risks can be compounded.
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