What Are Compound Drugs? Rule 134.500(4) defines “compounding” as the preparation, mixing, assembling, packaging, or labeling of a drug or device per.

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Presentation transcript:

What Are Compound Drugs? Rule (4) defines “compounding” as the preparation, mixing, assembling, packaging, or labeling of a drug or device per the Occupations Code Typically used for patients with allergies, specific medical conditions, and children

In Workers’ Compensation… The primary issue is “topicals” – creams, gels, or ointments that are applied to the skin.

Problems: Expensive! Can cost thousands of dollars, up to $14k Not supposed to be manufactured in bulk Multiple ingredients

Problems: Not Proven Effective Very little testing or oversight Not FDA approved Efficacy of drugs through dermal absorption has not been proven Accessed on March

Problems: Not Medically Necessary FDA approved drugs in pill form are typically available with no reason for the potentially ineffective topical cream

Problems: Duplicative & Risky Many compounds contain multiple drugs of the same variety with increased potency Compounds have led to deaths and illnesses in some cases The potential for large profits has lead to scams and kickback schemes

Why It’s An Issue Now: Mass Marketing

Why It’s An Issue Now: Increases

Potential Solutions: Pre Authorization Required for : (1)Any compound that contains an “N” drug (2)Investigational or experimental drugs Rule Accessed March

Potential Solutions: Retrospective Review & Non Closed Formulary Review for medical necessity afterwards, particularly since compounds are rarely determined necessary defines “closed formulary” as any FDA approved prescription or nonprescription drug except the three categories that require preauthorization. Compound drugs are not FDA approved.

Helpful Resources Research.pdf Research.pdf

THANK YOU!