W. Va. Code R. § 64-74-6 - Informed Consent Right
6.1.
In order for a consumer to give informed consent for care or treatment, a
behavioral health service shall inform him or her of the following:
6.1.a. The rights provided under this
rule;
6.1.b. The nature of his or
her condition and the treatment proposed;
6.1.c. Any reasonable alternative treatments
available;
6.1.d. That consent for
any part of treatment may be withdrawn at any time in writing or verbally to a
member of the treatment staff. Revocation of consent shall be documented on the
consent form, and further treatment shall not be provided except as authorized
in an emergency;
6.1.e. The reason
for taking a proposed medication, including the likelihood of the consumer's
condition improving or not improving without the proposed medication;
6.1.f. The type, dosage, including the use of
PRN (as needed) orders, the method of administration (oral or injection), and
the duration of taking the proposed medication; and
6.1.g. The common side effects, any side
effects probable with the particular consumer, and additional side effects that
may occur when taking the proposed medication longer than three (3)
months.
6.2. In the
absence of written consent, if treatment is provided to a consumer, he or she
has the right to documentation of the precipitating causes for providing the
treatment.
6.3. The procedures
outlined in this section shall not apply to those individuals who:
6.3.a. Need life-saving medication for
chronic medical conditions, such as diabetes or heart disease; or
6.3.b. Have been taking medications prior to
admission and have not refused to continue the medication, even though they may
not be able to give informed consent.
Notes
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