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Journal of the American Academy of Dermatology
Sous presse. Epreuves corrigées par l'auteur. Disponible en ligne depuis le lundi 17 février 2020
Doi : 10.1016/j.jaad.2019.11.061
accepted : 26 November 2019
Regulations, liability, safety, and economics related to compounding
 

Elliott H. Campbell, MD a, , Dirk M. Elston, MD b, Chad L. Straughan, PharmD c, Diana D. Antonovich, MD d
a Indiana University School of Medicine, Indianapolis, Indiana 
b Department of Dermatology and Dermatologic Surgery, Medical University of South Carolina, Charleston, South Carolina 
c Tidewater Pharmacy & Medical Supply, Charleston, South Carolina 
d Department of Dermatology and Dermatologic Surgery, Medical University of South Carolina, Charleston, South Carolina 

Correspondence to: Elliott H. Campbell, MD, 716 Timberline Dr, Villa Hills, KY 41017.716 Timberline Dr, Villa HillsKY41017
Abstract

Extemporaneous compounding is a means to tailor a medication to an individual patient's needs and may be required when no commercial product exists to meet that need. Compounded products range from buffered lidocaine to topical creams and ointments. Recent heightened regulations have made compounding more challenging for dermatologists and prompted this review of regulations, liability, and safety related to compounding. With this information, providers may minimize liability and maximize safety while caring for their patients.

The full text of this article is available in PDF format.

Key words : botulinum toxin, compounding, cost, economics, financial, formulation, levigation, lidocaine, regulations, regulatory requirements, safety

Abbreviations used : FDA, USP



 Funding sources: None.
 Conflicts of interest: None disclosed.



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