Legal analysis: In order to implement the "Prescription Management Measures", standardize hospital prescription management, improve prescription quality, promote rational use of drugs, and ensure medical safety. This system is formulated in accordance with relevant laws and regulations such as the Practicing Physician Law, the Drug Administration Law, the Regulations on the Administration of Pharmaceutical Affairs in Medical Institutions, the Regulations on the Administration of Narcotic Drugs and Psychotropic Drugs, and in combination with the actual situation of the hospital.

Legal basis: "Prescription Management Measures"

Article 10 Prescription writing must comply with the following rules:

(1) The general patient items recorded in the prescription should be clear , complete, and consistent with medical records.

(2) Each prescription is limited to one patient.

(3) The handwriting of the prescription should be clear and must not be altered. If there is any modification, you must sign the modification and indicate the date of modification.

(4) Prescriptions must be written in standardized Chinese or English names. Medical, preventive, and health care institutions, physicians, and pharmacists are not allowed to prepare abbreviated names or use code names for drugs on their own. The name, dosage, specification, usage, and dosage of the drug must be written accurately and standardly, and ambiguous words such as "follow the doctor's advice" and "for personal use" are not allowed.

(5) Age must be written in full, and for infants and young children, the age in days and months. If necessary, infants and young children should indicate their weight. Western medicines, Chinese patent medicines, and Chinese medicine preparations must be prescribed separately.

(6) For prescriptions of Western medicines and Chinese patent medicines, each medicine must be on a separate line. No more than five drugs may be prescribed per prescription.

(7) When writing prescriptions for traditional Chinese medicine pieces, they can be arranged in the order of monarch, minister, assistant, and envoy; special requirements for medicine dispensing and decoction are indicated above the medicine, and brackets are added, such as cloth Wrap, fry first, add later, etc.; there are special requirements for the place of origin and processing of the drug, which should be written before the name of the drug.

(8) Dosage. Generally, the dosage should be used in accordance with the usual dosage in the drug instructions. If excessive dosage is required in special circumstances, the reason should be stated and signed again.

(9) In order to facilitate the review of prescriptions by pharmaceutical professionals and technicians, when doctors issue prescriptions, they must indicate the clinical diagnosis except in special circumstances.

(10) The blank space after issuing a prescription should be marked with a slash to indicate completion of the prescription.

(11) The signature style and special signature of the prescriber must be consistent with the style retained in the pharmaceutical department for reference, and shall not be changed arbitrarily, otherwise the sample must be re-registered for record keeping.