Legal and Ethical Considerations in Dispensing Flashcards
The written order and instruction of a validly registered authority for the use of a specific drug product for a specific patient.
Prescription
The act by a registered pharmacist of filling the prescription or a prescriber’s order.
Dispensing
Identification of drugs and medicines by their scientifically and internationally recognized active ingredients or by their official names as determined by FDA.
Generic Name
Prescribing drugs or medicines using their generic names or generic terminology.
Generic Prescribing
Dispensing the patient’s /buyer’s choice from among generic equivalent, e.g. finished pharmaceutical products having the same active ingredient(s), same dosage form and same strength as he prescribed drug.
Generic Dispensing
An act regulating and modernizing the practice of pharmacy in the Philippines, repealing for the purpose R.A. No. 5921, otherwise known as the Pharmacy Law
REPUBLIC ACT NO. 10918 - “PHILIPPINE PHARMACY ACT”
refers to the sum of processes performed by a pharmacist from reading, validating, and
interpreting prescriptions; preparing; packaging; labeling; record keeping: dose calculations; and counseling or giving information, in relation to the sale or transfer of pharmaceutical products, with or without a prescription or medication order.
Dispensing
Compounding and dispensing shall be done only by duly registered and licensed pharmacists, in accordance with
Good Manufacturing Practice
All prescriptions and pharmacist-only OTC medicines shall be filled, compounded and
dispensed only by a registered and licensed pharmacist, in accordance with the Philippine Practice Standards for Pharmacists, Dispensing Guidelines and other standards pertaining to purity, safety and quality.
Filling and Partial Filling of Prescription
Partial filling of prescription less than the total quantity indicated in the prescription shall be _______
allowed
Pharmaceutical products given or intended to be given free to any health professional by
a manufacturer or distributor or its professional service representative as part of its program or promotion shall not be sold to any pharmaceutical outlet or the consuming public.
Physician’s Sample
Upon every box, bottle, or package of medicines compounded or dispensed by a
registered and licensed pharmacist based on prescription, there shall be pasted, affixed, or imprinted a seal or label bearing the ………..
name of patient and generic name of drug; brand name, if any, strength, expiry date, directions for use; and name and address of pharmacy, name of the doctor, the dispensing pharmacist
containing special pharmacists’ instructions for the patient shall be required as prescribed for dangerous drugs, external-use-only drugs, drugs with special storage and administration instructions and such other drugs as may be required by law.
Auxiliary labels
An act to promote, require and ensure the production of an adequate supply, distribution, use and acceptance of drugs and medicines identified by their generic names
REPUBLIC ACT NO. 6675 - “GENERICS ACT OF 1988”
REPUBLIC ACT NO. 6675
GENERICS ACT OF 1988