Which term denotes compounding with non-sterile ingredients?

The term that denotes compounding with non-sterile ingredients is high-risk compounding. This classification applies specifically to situations where the compounded medication is made from non-sterile products and poses a higher risk of contamination or incorrect dosage. Such risks necessitate stringent controls and processes to mitigate potential patient harm.

High-risk compounding often involves ingredients or conditions that lack the required sterility attributes—or are exposed to environments that may not adhere to sterile standards. It can include open systems, prolonged storage of compounded products, or mixing non-sterile ingredients to create a final product.

In contrast, low-risk compounding typically involves sterile ingredients and requires less stringent controls, while medium-risk compounding applies to more complex processes than low-risk but still involves sterile conditions. Immediate-use compounding refers to preparations that are made for immediate patient administration and must be used quickly to maintain their safety and effectiveness. Each of these terms serves to classify the level of risk associated with compounding practices based on the sterility of ingredients and the environment in which they are processed.