Microbial contamination of nonsterile pharmaceuticals in public hospital settings

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dc.contributor.author Mugoyela, V.
dc.contributor.author Mwambete, K.
dc.date.accessioned 2015-10-07T14:47:32Z
dc.date.available 2015-10-07T14:47:32Z
dc.date.issued 2010-09-09
dc.identifier.citation Mugoyela, V., & Mwambete, K. D. (2010). Microbial contamination of nonsterile pharmaceuticals in public hospital settings. Therapeutics and clinical risk management, 6, 443. en_GB
dc.identifier.issn 10.2147/TCRM.S12253
dc.identifier.uri http://hdl.handle.net/123456789/1630
dc.description The authors report no conflicts of interest in this work en_GB
dc.description.abstract Purpose: Contamination of pharmaceuticals with microorganisms irrespective whether they are harmful or nonpathogenic can bring about changes in physicochemical characteristics of the medicines. Although sterility is not a requirement in official compendia for nonsterile pharmaceuticals, bioburdens need to be within acceptable limits. Therefore, this study investigated microbial contamination of 10 nonsterile pharmaceuticals frequently delivered to outpatients by identifying and quantifying microbial contaminants and susceptibility pattern testing on the microbes isolated. Methods: The study was carried out at Amana Municipal Hospital in Dar es Salaam, Tanzania. The protocol for the study involved structured selection of representative tablets, syrups, and capsules from the hospital’s outpatient pharmacy. Constitutive microorganisms were elaborated and enumerated using standard microbiologic procedures. Results: Results showed that 50% of all tested products were heavily contaminated, and the predominant contaminants comprised Klebsiella, Bacillus, and Candida species. Furthermore, the results showed that the isolated Bacillus and Klebsiella species were resistant to Augmentin ® and cloxacillin. The differences in means for cfu/mL and zones of inhibition among the microorganisms isolated were considered significant at P , 0.05. Conclusion: The nonsterile pharmaceuticals were presumably microbiologically contaminated due to poor handling during dispensing, repackaging, and/or nonadherence to good manufacturing practice. Therefore, training and educating the dispensers, as well as patients, on the proper handling and use of medicines cannot be overemphasized, because these are key aspects in controlling cross-contamination of medicines. en_GB
dc.description.sponsorship Ministry of Science, Technology and Higher Education en_GB
dc.language.iso en en_GB
dc.publisher Dovepress en_GB
dc.relation.ispartofseries Therapeutics and Clinical Risk Management;
dc.subject Microorganisms en_GB
dc.subject Outpatients en_GB
dc.subject Pharmacy en_GB
dc.subject Bioburdens en_GB
dc.subject Dispensing en_GB
dc.title Microbial contamination of nonsterile pharmaceuticals in public hospital settings en_GB
dc.type Article en_GB


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