Assessment of practice and perceptions of healthcare professionals regarding the contribution of inappropriate pharmaceutical compounding to adverse drug events (ADEs) and antimicrobial resistance (AMR)

Author:

Ayenew Wondim,Bitew Teshome,Mohammed Abdulwase,Mengesha Assefa kebad,Chanie Gashaw Sisay,Mitku Melese Legesse,Melese Mihret,Gela Yibeltal Yismaw,Beyna Alemante Tafese,Esubalew Dereje,Simegn Wudneh,Limenh Liknaw Workie

Publisher

Springer Science and Business Media LLC

Reference39 articles.

1. Galson SK. Federal and state role in pharmacy compounding and reconstitution: exploring the right mix to protect patients. Hearing on oversight before the senate comm. on health, education, labor, & pensions, 108th Cong. 2003. http://www.fda.gov/NewsEvents/Testimony/ucm115010.htm.

2. Yuliani SH, Putri DCA, Virginia DMSH, Gani MR, Riswanto FDO. Prevalence, risk, and challenges of extemporaneous preparation for pediatric patients in developing nations: a review. Pharmaceutics. 2023;15:840. https://doi.org/10.3390/pharmaceutics15030840.

3. U.S. Food & Drug Administration. FDA alerts health care professionals and compounders of potential risks associated with the compounding of remdesivir drug products. Updated 02/04/2021

4. Smith A, Jones JK, Wu S. Compounded medications: a systematic review. J Pharm Sci. 2020;109(7):2211–26.

5. Lee H, Woodcock J, Mazer-Amirshahi M, et al. US food and drug administration approval of flibanserin: even the score does not add up. JAMA Intern Med. 2019;179(10):1402–3.

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