
COMPOUNDINGPREPACK LOG Form
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People also ask
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Which of the following components must be included in a compounding record?
Final answer: A compounding record must include several key components such as BUD, route of administration, drug name, instructions for preparing the CNSP, manufacturer of all ingredients, and drug dosage form. Each of these elements plays a critical role in ensuring safe and accurate compounding.
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What are the requirements for level A compounding?
Level A Response Level A preparations are compounded in a designated, non-sterile compounding area that is large enough for compounding personnel to work comfortably and safely, with room to store equipment and products in an orderly manner, and is located in clean and secure surroundings.
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What is compounding and repackaging in epic?
Compounding and repackaging records represent the products created when pharmacists combine multiple medications to create a new medication or take one medication from a container and place it into another container.
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What is the Anteroom for compounding?
The anteroom is usually equipped with a sink, cabinets and a bench, but equipment and activities in this area must be kept to a minimum. The anteroom can be engineered as an ISO 7 or ISO 8 environment depending on the risk level (HD or non-HD) of the sterile products being prepared in the critical area.
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What is required on a compounding record?
Description of ingredients, their quantities and sources (e.g., physical description, DIN, manufacturer, etc.) Quality control procedures and expected results (e.g., weight range of filled capsules, pH of aqueous liquids, etc.) Mixing instructions and methods, which may include: order of mixing.
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What are the five general steps in compounding process?
General Steps in the Compounding Process Receiving and checking for completeness and authenticity of the recipe. Clarifying with the doctor or patient about any missing information. Calculating drug dosages and checking for drug interactions. Calculating the amount of drugs and excipients to be used.
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What is a compounding log?
A Compounding Record (CR) is a document that records the preparation of a compounded medication. It is important to maintain compounding records to demonstrate compliance with USP standards. For nonsterile preparations, a CR must be created for all preparations to ensure the traceability of all components.
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What must be documented in the compounding record?
The information that needs to be documented in a compound record includes name, dose, and strength of the drug; master formulation record information; ingredients; total amount produced; name of all pharmacists involved in the compounding; date; prescription number; label information; and quality control information.
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