As required by both the HCS (General) Regulations 2021 and the Health Products Regulations 2016, medical practitioners should record details including the product name, amount supplied and dose instructions to patients to ensure that the appropriate dose has been prescribed and dispensed or administered to the correct patient. Patient’s medication records should contain adequate, accurate and relevant information to ensure clear documentation, and safe and appropriate use of the product by the patient.

Any pertinent information in relation to the supply of medications to patients should be recorded accordingly (e.g., drug allergies, G6PD deficiency, medication history, dietary information).