Chapter II General Principles of Prescription Management

Article 5. Prescription standards (annex 1) shall be uniformly stipulated by the Ministry of Health, and the prescription format shall be determined by provinces, autonomous regions and municipalities directly under the Central Government? The provincial health administrative department (hereinafter referred to as the provincial health administrative department) uniformly formulates prescriptions, which are printed by medical institutions in accordance with the prescribed standards and formats.

Article 6 Prescription writing shall follow the following rules:

(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) The name of a drug shall be written in a standardized Chinese name; if there is no Chinese name, it may be written in a standardized English name;

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) the 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 on the upper right of the drug, 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.

Article 7. Dosage and quantity of drugs should be written in Arabic numerals. Dose should use legal dosage units: weight is in grams (g), milligrams (mg), micrograms (μg) and nanograms (ng); Capacity units are liters (L) and milliliters (mL); International unit (IU), unit (u); The unit of Chinese herbal pieces is gram (g).

Tablets, pills, capsules and granules are used as tablets, pills, granules and bags respectively; The solution is in rods and bottles; Ointment and cream are in the form of sticks and boxes; Injections are in sticks and bottles, and the content should be indicated; Chinese herbal pieces take dosage as the unit.

Extended data:

Brief introduction of prescription management methods

In order to standardize prescription management, improve prescription quality, promote rational drug use, and ensure medical safety, these measures are formulated in accordance with the Law on Medical Practitioners, the Drug Administration Law, the Regulations on the Administration of Medical Institutions, and the Regulations on the Administration of Narcotic Drugs and Psychotropic Drugs.

The Measures are divided into general principles, general principles of prescription management, acquisition of prescription rights, prescription issuance, prescription adjustment, supervision and management, legal responsibilities and supplementary provisions, with a total of 8 chapters and 63 articles.

On October 27th, 2006, approved by People's Republic of China (PRC). The ministerial meeting of the Ministry of Health discussed and passed, which was promulgated on February 14, 2007 and implemented on May 1 2007. At the same time, the Measures for the Administration of Prescriptions (for Trial Implementation) and the Provisions on the Administration of Prescriptions of Narcotic Drugs and Psychotropic Substances shall be abolished.

Reference: Baidu Encyclopedia-Prescription Management Measures