{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,4]],"date-time":"2026-05-04T07:20:41Z","timestamp":1777879241088,"version":"3.51.4"},"reference-count":10,"publisher":"SAGE Publications","issue":"1","license":[{"start":{"date-parts":[[2017,11,23]],"date-time":"2017-11-23T00:00:00Z","timestamp":1511395200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["Therapeutic Advances in Drug Safety"],"published-print":{"date-parts":[[2018,1]]},"abstract":"<jats:p>Dabigatran is a newer oral direct thrombin inhibitor approved by the United States Food and Drug Administration and the European Medicines Agency (EMA). The proper dosage of the drug, the potential for adverse drug reactions and the nature of bleeds with use of this drug as with other novel oral anticoagulants (NOACs), in the elderly population are still areas of uncertainty. Despite the existence of a specific antibody, idarucizumab which is an antidote to dabigatran toxicity, management of dabigatran-induced bleeds is an undefined area especially in resource constrained settings. We report severe haematuria with dabigatran in three elderly Indian patients at the lowest recommended therapeutic dose and explore these grey zones in dabigatran therapy.<\/jats:p>","DOI":"10.1177\/2042098617742344","type":"journal-article","created":{"date-parts":[[2017,11,23]],"date-time":"2017-11-23T07:23:04Z","timestamp":1511421784000},"page":"89-91","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":4,"title":["Severe haematuria of lower urinary tract origin with low dose dabigatran use in three Indian elderly patients: unresolved issues in the safety of novel oral anticoagulants"],"prefix":"10.1177","volume":"9","author":[{"given":"Upinder","family":"Kaur","sequence":"first","affiliation":[{"name":"Department of Pharmacology (Previously Division of Geriatrics, Department of General Medicine), Institute of Medical Sciences, Banaras Hindu University, Varanasi, UP, India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sankha Shubhra","family":"Chakrabarti","sequence":"additional","affiliation":[{"name":"Division of Geriatrics, Department of General Medicine, Institute of Medical Sciences, Banaras Hindu University, Varanasi, UP, India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sukdev","family":"Manna","sequence":"additional","affiliation":[{"name":"Department of General Medicine, Institute of Medical Sciences, Banaras Hindu University, Varanasi, UP, India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Indrajeet Singh","family":"Gambhir","sequence":"additional","affiliation":[{"name":"Division of Geriatrics, Department of General Medicine, Institute of Medical Sciences, Banaras Hindu University, Varanasi-221005, UP, India"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"179","published-online":{"date-parts":[[2017,11,23]]},"reference":[{"key":"bibr1-2042098617742344","unstructured":"Food and Drug Administration. 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