(a) Prior to or simultaneously with dispensing a prescription in accordance with sections 17b-260 to 17b-262, inclusive, and 17b-264 to 17b-285, inclusive, a pharmacist or the designee of the pharmacist shall make a reasonable effort to obtain, record and maintain, in a manner deemed appropriate by the pharmacist, the following information regarding the individual receiving such prescription: (1) Name, address, telephone number, date of birth or age and gender; (2) individual history where significant, including disease states, known allergies and drug reactions; (3) a comprehensive list of drugs and relevant devices dispensed by the pharmacy within the last one hundred eighty days; and (4) the pharmacist's comments relevant to the individual's drug therapy.
(b) Prior to or simultaneously with dispensing a drug to an individual eligible for benefits in accordance with sections 17b-260 to 17b-262, inclusive, and 17b-264 to 17b-285, inclusive, a pharmacist shall undertake a review of drugs dispensed to the individual by the pharmacy during the previous one hundred eighty days. The review shall include screening for potential drug therapy problems due to therapeutic duplication, a contraindication between a drug and a disease, the interaction of one drug with another, incorrect drug dosage or duration of drug treatment, the interaction of a drug and an allergy, clinical abuse or misuse and any other significant clinical issues relating to the appropriate use of drugs. Such review shall be based upon current standards and information consistent with that provided in the following resources: The American Hospital Formulary Service Drug Information, the United States Pharmacopoeia Drug Information, the American Medical Association Drug Evaluations and the peer-reviewed medical literature.
(c) Prior to or simultaneously with dispensing drugs to individuals eligible for benefits in accordance with sections 17b-260 to 17b-262, inclusive, and 17b-264 to 17b-285, inclusive, a pharmacist shall, whenever practicable, offer in person to discuss the drugs to be dispensed and to counsel the client on their usage, except when the person obtaining the prescription is other than the person named on the prescription form or the pharmacist determines it is appropriate to make such offer in writing. Any such written offer shall include an offer to communicate with the client either in person at the pharmacy or by telephone.
(d) The discussion and counseling offered in accordance with subsection (c) of this section shall include information deemed significant by the pharmacist based upon the findings of the review conducted in accordance with subsection (b) of this section, including (1) the name and description of the drug; (2) dosage form, dosage, route of administration and duration of drug therapy; (3) special directions and precautions for preparation, administration and use by the patient; (4) common severe side or adverse effects or interactions and therapeutic contraindications or precautions which the pharmacist deems relevant; (5) techniques for self-monitoring drug therapy; (6) proper storage; (7) prescription refill information; and (8) action to be taken in the event of a missed dose or adverse reaction.
(e) Nothing in this section shall be construed as requiring a pharmacist to provide counseling or gather information when an individual receiving benefits refuses such counseling or refuses or is unable to provide the information requested. The pharmacist shall document the provision of counseling, a refusal by or the inability of the patient to accept counseling or a refusal by the patient to give information. Records kept pursuant to this subsection shall be maintained for the same length of time as prescription records are maintained pursuant to section 20-615.
(f) The provisions of subsections (c) and (d) of this section shall not apply to a drug dispensed to a patient of a nursing home that is in compliance with the requirements of 42 CFR 483.60.
(May Sp. Sess. P.A. 92-16, S. 41, 89; P.A. 95-264, S. 41.)
History: P.A. 95-264 moved provisions of Subsec. (d) to Subsec. (a), relettering Subsecs. as necessary and made technical changes; Sec. 20-185g transferred to Sec. 20-620 in 1997.
Structure Connecticut General Statutes
Section 20-570. - Short title: Pharmacy Practice Act.
Section 20-571. (Formerly Sec. 20-184a). - Definitions.
Section 20-572. (Formerly Sec. 20-163). - Commission of Pharmacy. Appointment and term of members.
Section 20-573. (Formerly Sec. 20-165). - Meetings of commission. Records.
Section 20-574. (Formerly Sec. 20-164a). - Supervision by Commissioner of Consumer Protection.
Section 20-575. - Powers and responsibilities.
Section 20-576. (Formerly Sec. 20-164). - Regulations.
Section 20-576a. - Acceptance and disposal of unused prescription drugs at pharmacies. Regulations.
Section 20-578. (Formerly Sec. 21a-306). - Information not to be disclosed. Exception.
Section 20-580. (Formerly Sec. 20-167). - Revocation or suspension of nonlegend drug permit.
Section 20-581. (Formerly Sec. 20-185). - Penalty for violation of Pharmacy Practice Act. Exception.
Section 20-582. (Formerly Sec. 20-176). - Appeals of decisions of Commission of Pharmacy.
Section 20-583. - Where appeals returnable.
Section 20-591. - Graduates of foreign pharmacy schools. Regulations.
Section 20-596. (Formerly Sec. 20-168b). - Ownership of pharmacies by prescribing practitioners.
Section 20-598. (Formerly Sec. 20-177). - Registration of pharmacy interns.
Section 20-598a. - Registration and certification of pharmacy technicians.
Section 20-599. (Formerly Sec. 20-174a). - Continuing education: Definitions.
Section 20-605. - Practice of pharmacy without license or temporary permit prohibited.
Section 20-606. (Formerly Sec. 20-178). - Use of the title “pharmacist”.
Section 20-611. (Formerly Sec. 20-175b). - Advertising legend drug prices.
Section 20-612. - Only pharmacy may accept prescription for dispensing.
Section 20-617a. - Flavoring agent added to prescription product.
Section 20-618. (Formerly Sec. 21a-107). - Repackaged drugs not considered misbranded, when.
Section 20-623. - Sale of nonlegend drugs. Labels, packaging and contents. Penalty.
Section 20-624. - Permit to sell nonlegend drugs.
Section 20-625. - Nonlegend veterinary drugs.
Section 20-626. - Confidentiality of pharmacy records.
Section 20-627. - Nonresident pharmacy. Definitions. Certificate of registration. Requirements.
Section 20-628. - Shipping, mailing or delivering legend devices or drugs.
Section 20-630. - Advertising.
Section 20-633. - Administration of vaccines by licensed pharmacists. Regulations.
Section 20-633a. - Pharmacy rewards program. Plain language summary. Violation.
Section 20-633b. - Sterile compounding pharmacies. Requirements. Regulations.
Section 20-633c. - Prescribing of opioid antagonists by licensed pharmacists. Regulations.
Section 20-633i. - Issuance of prescriptions for epinephrine auto injectors by pharmacists.
Section 20-636. - Sign re storage and disposal of prescription drugs.