University of Rwanda Digital Repository

Quality of oxytocin and misoprostol in health facilities of Rwanda

Show simple item record

dc.contributor.author Bizimana, Thomas
dc.contributor.author Nhomsai, Hagen
dc.contributor.author Gesa, Gnegel
dc.contributor.author Kayumba †, Pierre Claver
dc.contributor.author Lutz, Heide
dc.date.accessioned 2022-03-09T09:57:50Z
dc.date.available 2022-03-09T09:57:50Z
dc.date.issued 2021-01-08
dc.identifier.issn e0245054
dc.identifier.uri https://doi.org/10.1371/journal.pone.0245054
dc.identifier.uri http://hdl.handle.net/123456789/1528
dc.description Journal artiicle en_US
dc.description.abstract Sustainable Development Goal 3.1 calls for a reduction of the maternal mortality ratio to less than 70 per 100,000 live births by 2030. The most important cause of maternal mortality is post-partum haemorrhage (PPH). Oxytocin injections and misoprostol tablets are medicines of first choice for the management of PPH in low- and middle-income countries (LMICs). Unfortunately, both substances are chemically unstable, and previous studies have revealed serious quality problems of these medicines in LMICs. The present study is the first report on their quality in Rwanda. From 40 randomly selected health facilities (hospitals, health centers, retail pharmacies and private clinics) in different parts of Rwanda, as well as from six wholesalers and government stores, oxytocin injections and misoprostol tablets were collected. Oxytocin storage temperatures in the health facilities were monitored for six months using temperature data loggers, and found to correctly follow the storage requirements stated by the manufacturers (2–8°C, or room temperature) with few minor deviations. Oxytocin injections (57 samples, representing seven batches of four brands) were tested for their oxytocin content and pH value according to the United States Pharmacopeia. Twenty-four samples from three European manufacturers passed all tests. However, all nine samples of one batch of a Chinese manufacturer showed an excessive content of oxytocin (range 117.2–121.5% of the declared amount). Another batch of the same manufacturer showed extreme variations of the concentration of the preservative benzyl alcohol. Misoprostol tablets (25 samples, representing ten batches of six brands) were tested for content and dissolution according to the International Pharmacopoeia. Fifteen samples passed, but all 10 samples of two brands from India failed with extreme deviations, containing only 42.5–48.7% of the stated amount of misoprostol. In conclusion, oxytocin quality in Rwanda was better than reported from other African countries. However, two extremely substandard brands of misoprostol tablets were found. The Rwandan authorities reacted quickly and efficiently, and recalled these substandard medicines from the market. For oxytocin and misoprostol, with their well-known problems of quality and stability, procurement should possibly be restricted to medicines which are WHO-prequalified or which have been manufactured in countries with stringent regulatory authorities en_US
dc.language.iso en en_US
dc.publisher Plos one en_US
dc.relation.ispartofseries Vol.16 , no 1;
dc.subject Oxytocin; Oxytocin injections; maternal mortality; misoprostol en_US
dc.title Quality of oxytocin and misoprostol in health facilities of Rwanda en_US
dc.type Article en_US


Files in this item

Files Size Format View

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record

Search Repository


Browse

My Account