Get Physicians Instruction To Use A Medicine To Be Extemporaneously Prepared

A compounded medication may be more suitable than other products for several reasons. Examples include needing a specific strength or dosage that's not commercially available, needing to adjust a drug's route of administration, and needing to remove ingredients that you're allergic to.

Compounding practice includes activities such as formulating, mixing, or repacking products. Extemporaneous preparations are not licensed by Drug Regulatory Authorities and hence, are not evaluated for quality, efficacy, and stability. Also, adverse event reporting is not mandatory for these products.

Label extemporaneously prepared solutions with a 7-day expiration date, which is consistent with the shelf life recommended by the manufacturer. Store tablets and vials for intravenous (IV) administration at room temperature.

Extemporaneous compounding is done when certain medical needs of individual patients cannot be met by the use of an approved commercial drug product. There are several reasons a prescription may be compounded, but typically it is because the drug that a patient has been prescribed is not commercially available.

Extemporaneously compounded medicines may be useful when a required dose or dose form is unavailable commercially, or for individualised dosing. There are numerous established compounding formulae available, and new formulae may be developed with the help of formulation guidelines and professional advice.

A clear record in respect of each extemporaneously prepared product must be made and kept to ensure full traceability of the ingredients, formulae and method used, and the names of all pharmacists and staff members involved. The information to be recorded should be clearly documented in a written procedure.

Extemporaneous compounding is the science of preparing medicinal products for the treatment of a specific patient in the absence of an appropriate commercially available product.

The practice of extemporaneous compounding typically involves the small scale manufacture of preparations, using raw materials or commercially available dosage forms to formulate a suitable dosage form at an appropriate strength for a specific patient.