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General provisions of prescription management
Legal analysis: Prescription as mentioned in these Measures refers to the medical documents prescribed by registered medical practitioners and assistant medical practitioners (hereinafter referred to as doctors) for patients in their medical treatment activities, which are reviewed, prepared and checked by pharmaceutical professional technicians (hereinafter referred to as pharmacists) who have obtained the qualifications for pharmaceutical professional and technical positions, and serve as the medication vouchers for patients. Prescriptions include medical institution ward medication orders.

These Measures are applicable to medical institutions and their personnel related to prescription, dispensing and storage.

Legal basis: Prescription Management Measures

Article 5 Prescription standards (Annex 1) shall be uniformly formulated by the Ministry of Health, and prescription formats shall be uniformly formulated by the health administrative departments of all provinces, autonomous regions and municipalities directly under the Central Government (hereinafter referred to as provincial health administrative departments), and prescriptions shall be printed by medical institutions according to the prescribed standards and formats.

Article 6 Prescription writing shall meet the following requirements:

(a) the patient's general situation and clinical diagnosis are clearly and completely filled in, and are consistent with the medical records.

(two) each prescription is limited to one patient.

(3) The handwriting is clear and shall not be altered; If it is necessary to modify, it should be signed at the modification place and indicate the date of modification.

(4) A standardized Chinese name shall be used for the name of a drug; if there is no Chinese name, a standardized English name may be used; Yamatonokusushi, a medical institution or physician, shall not compile abbreviations or use codes by himself; The name, dosage, specification, usage and dosage of drugs should be accurate and standardized, and the usage of drugs can be written in standardized Chinese, English, Latin or abbreviations, but vague words such as "following doctor's advice" and "for personal use" should not be used.

(five) the patient's age should fill in the full age, the date and month age of the newborn and baby, and indicate the weight when necessary.

(six) western medicine and Chinese patent medicine can be prescribed separately, or a prescription, Chinese herbal pieces should be prescribed separately.

(seven) prescription of western medicine and Chinese patent medicine, each drug should be listed in a new line, each prescription shall not exceed 5 drugs.

(eight) the prescription of Chinese herbal pieces shall be written in the order of "monarch, minister, assistant and envoy"; The special requirements for dispensing and decocting drugs are indicated in the upper right of the drugs, and brackets are added, such as wrapping, frying first, dropping later, etc. Where there are special requirements for the origin and processing of the decoction pieces, it shall be indicated before the name of the drug.

(9) The usage and dosage of drugs shall conform to the conventional usage and dosage specified in the drug instructions. In case of overdose under special circumstances, the reasons shall be indicated and re-signed.

(ten) except in special circumstances, the clinical diagnosis should be indicated.

(eleven) draw a diagonal line in the blank after the prescription is issued, indicating that the prescription is finished.

(12) The signature style and special seal of the prescriber shall be consistent with the sample style kept by the hospital pharmacy department for future reference, and shall not be changed at will, otherwise it shall be re-registered.