Bill Text: MI HB4508 | 2009-2010 | 95th Legislature | Introduced
Bill Title: Health; pharmaceuticals; prohibition on redispensing a pharmaceutical; revise to allow pharmacists to place previously dispensed drugs in customized patient medication packages. Amends 1978 PA 368 (MCL 333.1101 - 333.25211) by adding sec. 17751a.
Spectrum: Bipartisan Bill
Status: (Introduced - Dead) 2009-03-05 - Printed Bill Filed 03/05/2009 [HB4508 Detail]
Download: Michigan-2009-HB4508-Introduced.html
HOUSE BILL No. 4508
March 4, 2009, Introduced by Reps. Caul, Ball, Booher, Sheltrown and Dean and referred to the Committee on Health Policy.
A bill to amend 1978 PA 368, entitled
"Public health code,"
(MCL 333.1101 to 333.25211) by adding section 17751a.
THE PEOPLE OF THE STATE OF MICHIGAN ENACT:
Sec. 17751a. (1) Notwithstanding any provision of this article
or article 7 to the contrary and subject to this section, a
pharmacist, upon the request of a patient or the patient's
caregiver, may place prescribed drug products in a customized
patient medication package regardless of whether the pharmacist
originally dispensed the drug products. If the pharmacist is
dispensing the drug products, he or she shall comply with R
338.479c of the Michigan administrative code. If previously-
dispensed drug products are brought to a pharmacist by a patient or
the patient's caregiver for placement in a customized patient
medication package under this section, all of the following
requirements shall be met:
(a) The pharmacist shall comply as much as possible with R
338.479c of the Michigan administrative code and identify for the
patient on a form prescribed by the department the portions of R
338.479c of the Michigan administrative code that he or she is
unable to comply with because he or she is repackaging drug
products previously dispensed by another pharmacy.
(b) The patient or the patient's caregiver shall complete and
sign a form prescribed by the department that describes the drug
products to be placed in the customized patient medication package,
authorizes the pharmacist to place the previously-dispensed drug
products in a customized medication package, and releases the
pharmacist who places the drug products in a customized medication
package from liability as provided for under subsection (3).
(c) The patient or the patient's caregiver shall deliver the
drug products to the pharmacist in their original containers
bearing the labels required for prescription drug products under
this act and federal law.
(d) The pharmacist shall maintain complete records of drug
products placed in customized patient medication packages under
this section and maintain those records in the same manner and for
the same period of time as is required for other records of drug
products dispensed under this article.
(e) If the pharmacist does not immediately place the drug
products in customized patient medication packages under this
section, the pharmacist shall store the drug products in a secure
location and under conditions that will maintain their stability,
integrity, and effectiveness until placed in the customized patient
medication package under this section and returned to the patient
or the patient's caregiver.
(2) A pharmacist who is not certain that previously-dispensed
drug products are exactly as described on the prescription drug
container's label shall not place the drug products in a customized
patient medication package under this section.
(3) A pharmacist who places previously-dispensed drug products
in a customized patient medication package in compliance with this
section is immune from civil liability arising from harm caused by
1 or more of the drug products due to acts or omissions of other
persons outside of the control of the pharmacist.
(4) This section does not require a pharmacist to place any
drug product in a customized patient medication package. A
pharmacist may charge a reasonable fee for placing drug products in
customized patient medication packages under this section.
(5) Before the expiration of 90 days after the effective date
of this section, the department shall create and make widely
available to pharmacists the forms required under this section.
(6) This section applies to pharmacists after the expiration
of 90 days after the effective date of this section.