| dc.contributor.author | Shukla, Pooja | |
| dc.contributor.author | Bansode, F W | |
| dc.contributor.author | Singh, R K | |
| dc.date.accessioned | 2012-06-27T11:11:28Z | |
| dc.date.available | 2012-06-27T11:11:28Z | |
| dc.date.issued | 2011 | |
| dc.identifier.citation | Journal of Medicine and Medical Sciences 2011, 2(13), 1313-1316 | en |
| dc.identifier.uri | http://hdl.handle.net/123456789/785 | |
| dc.description.abstract | Chloramphenicol (CAP) is a potent and efficient antibiotic used since years against many pathogens. Despite being highly effective, it shows severe toxicity in the form of Aplastic anemia (AA) and bone marrow suppression. Its D – form is the toxic one and inhibits protein synthesis. In living system, CAP is hydrolyzed and absorbed completely. Its excretion is also at a high rate but is highly impaired in disorders associate liver and kidneys. It is metabolized in liver to Chloramphenicol glucuronide. Being highly toxic, it is still prescribed at a noticeable rate. It is recommended to be prescribed to be only when there is no other alternative is present with a monitoring of its concentration in patients body. Chloramphenicol induced hematotoxicity was demonstrated in rats which recovered due to oral administration of coconut water within two weeks. | en |
| dc.format.extent | 54603 bytes | |
| dc.format.mimetype | application/pdf | |
| dc.language.iso | en | en |
| dc.relation.ispartofseries | CDRI Communication No. 8195 | en |
| dc.subject | Chloramphenicol | en |
| dc.subject | Toxicity | en |
| dc.subject | antibiotic | en |
| dc.subject | Aplastic anemia | en |
| dc.subject | hematotoxicity | en |
| dc.title | Chloramphenicol Toxicity: A Review | en |
| dc.type | Article | en |