Extemporaneous Compounding and Safety in Pharmacy

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These flashcards cover key vocabulary related to extemporaneous compounding, including definitions, processes, and important distinctions in pharmacy practice.

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29 Terms

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Extemporaneous Compounding

The preparation, mixing, assembling, packaging, or labeling of a drug or device based on specific patient needs instead of for mass distribution.

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NABP Model State Pharmacy Act

Defines the standards for the practice of compounding pharmacists and establishes the criteria for drug preparation.

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Therapeutic Outcome

The final result or effect of a medical treatment, aimed at achieving a positive impact on patient health.

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Compounding Pharmacist

A licensed pharmacist who prepares customized medications to meet individual patient needs.

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Surfactant

A substance that reduces surface tension and helps dissolve water-insoluble drugs in compounding.

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USP

United States Pharmacopeia; a standard setting organization that establishes guidelines for medicines.

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Unsolicited Prescription

A prescription for compounding that is given without solicitation or request by the pharmacist.

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Compounding vs Manufacturing

Compounding tailors medications for individual patients, while manufacturing produces drugs for mass market.

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Bioequivalence

The term used to describe when two drugs release the same amount of active ingredient in the same time frame. (Brand/Generic plasma conc is the same)

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Small Scale Preparation

Production of compounded drugs in small quantities tailored to individual needs.

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Economic Considerations in Compounding

Factors affecting the range of drug dosages and forms available in compounding due to costs.

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Specific Patient Needs

Unique requirements of an individual patient that may necessitate compounded medications.

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Orphan Drugs

Medications developed for rare diseases affecting small populations, often compounded due to scarcity.

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Customized Medications

Medications tailored specifically to an individual patient’s needs and conditions.

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Dosage Form

The physical form of a medication, such as tablet, capsule, liquid, etc., which affects its delivery and absorption.

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Delayed Release

A formulation designed to release medication at a specific time after administration.

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Gastro-retentive Dosage Form

A type of formulation designed to remain in the stomach for an extended period to improve absorption.

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Compounding Errors

Mistakes that occur during the preparation of compounded medications, which can lead to serious patient harm.

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Safety Focus in Pharmacy

The emphasis on ensuring the safety and accuracy of compounded medications to prevent errors.

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Recommended Practices in Compounding

Best practices such as verifying formulas and conducting safety checks during the preparation process.

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Low-Carbohydrate Preparations

Compounded formulations designed specifically for patients requiring low carbohydrate intake.

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Veterinary Compounding

The preparation of customized medications specifically formulated for animals, including pets and exotic species.

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Palatable Liquid Medications

Custom formulations that improve taste to facilitate administration, especially for children.

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Sustained-Release Therapy

A type of medication designed to release the active ingredient over an extended period.

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Chronotherapeutics

Treatment targeting specific times for medication administration based on the body’s circadian rhythms.

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Chemical Synthesis

The process of creating drugs through chemical reactions rather than extracting them from natural sources.

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Legal Restrictions on Compounding

  • Cannot be commercial product

  • Prescription must be unsolicited

  • Compounding of the prescription must be necessary

  • Compounding product must be substantially different from commercially available products

  • Do not compound for the physician’s office

  • One can compound prior to receiving a prescription IF they have history of receiving prescriptions for a product and only in small quantities

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3 main differences between manufacturing and compounding?

  1. Physician-patient-pharmacist relationship

  2. Quantity of product (Small amounts for a compounding pharmacist)

  3. Compounding is limited to a prescription order while manufacturing is for public at large

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How to improve therapeutic outcomes?

  • Avoidance of unwanted dyes, preservatives, fillers and active ingredients

  • Palatable liquid medications

  • Administrable dosage forms

  • Potential minimization or avoidance of side ffects

  • Combination or sustaned0release therapy to improve compliance

  • Unique dosage form for specific problems