Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Mo Dimbil"'
Autor:
Matthew S. Duprey, Nada S. Al-Qadheeb, Nick O’Donnell, Keith B. Hoffman, Jonathan Weinstock, Christopher Madias, Mo Dimbil, John W. Devlin
Publikováno v:
Drugs - Real World Outcomes, Vol 6, Iss 3, Pp 141-149 (2019)
Abstract Background Serious cardiovascular adverse events (SCAEs) associated with intravenous sedatives remain poorly characterized. Objective The objective of this study was to compare SCAE incidence, types, and mortality between intravenous benzodi
Externí odkaz:
https://doaj.org/article/2625593ca96d4f1da067c62052105c9c
Publikováno v:
PLoS ONE, Vol 7, Iss 8, p e42866 (2012)
BACKGROUND: Cholesterol management drugs known as statins are widely used and often well tolerated; however, a variety of muscle-related side effects can arise. These adverse events (AEs) can have serious impact, and form a significant barrier to the
Externí odkaz:
https://doaj.org/article/e0a0201c996a455ba5a659d3de16dd82
Publikováno v:
Drug Safety. 41:357-361
The Janus kinase (JAK) inhibitor baricitinib is approved in Europe and Japan for the treatment of rheumatoid arthritis. In April 2017, the US FDA expressed concern about thromboembolic events (deep venous thrombosis [DVT] and pulmonary embolism [PE])
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21fb5b5e89828329f8caca6099519acf
https://doi.org/10.1007/s40264-017-0622-2
https://doi.org/10.1007/s40264-017-0622-2
Publikováno v:
Drug Safety. 39:561-575
Many serious drug adverse events (AEs) only manifest well after regulatory approval. Therefore, the development of signaling methods to use with post-approval AE databases appears vital to comprehensively assess real-world drug safety. However, with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cef493eba8198c7b8ca963d06923b61a
https://doi.org/10.1007/s40264-016-0409-x
https://doi.org/10.1007/s40264-016-0409-x
Publikováno v:
Drug Safety
Background The US Food and Drug Administration (FDA) uses the Adverse Event Reporting System (FAERS) to support post-marketing safety surveillance programs. Currently, almost one million case reports are submitted to FAERS each year, making it a vast
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::892ac6568635bb4993217161793a7beb
http://europepmc.org/articles/PMC4206770
http://europepmc.org/articles/PMC4206770
Publikováno v:
Critical Care Medicine. 40:1-328
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::45c9ed80a5447e5c1f765d886f8381b7
https://doi.org/10.1097/01.ccm.0000425342.87405.2f
https://doi.org/10.1097/01.ccm.0000425342.87405.2f
Autor:
Nicholas P. Tatonetti, Mo Dimbil, Keith B. Hoffman, Colin B. Erdman, Andrea Demakas, Robert F. Kyle, Brian M. Overstreet, Dingguo Chen
Publikováno v:
Journal of managed carespecialty pharmacy. 21(12)
Given the multiple limitations associated with relatively homogeneous preapproval clinical trials, inadequate data disclosures, slow reaction times from regulatory bodies, and deep-rooted bias against disclosing and publishing negative results, there
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee93309bc571230fd853b3c74c0a3e97
https://pubmed.ncbi.nlm.nih.gov/26679963
https://pubmed.ncbi.nlm.nih.gov/26679963
Publikováno v:
Drug Safety
Background The United States Food and Drug Administration’s (FDA) Adverse Event Reporting System (FAERS) consists of adverse event (AE) reports linked to approved drugs. The database is widely used to support post-marketing safety surveillance prog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5ca98531469bc5c44e92d3baaec7546
https://pubmed.ncbi.nlm.nih.gov/24643967
https://pubmed.ncbi.nlm.nih.gov/24643967
Publikováno v:
BMJ (Clinical research ed.). 348
Anticoagulants are some of the most widely used drugs worldwide. Dabigatran is commonly assumed to be safer than warfarin, but because debate continues on this question,1 we analysed post-marketing safety signals across this drug class. Drug safety a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef4e23e6af36f172ad74e2708010afce
https://pubmed.ncbi.nlm.nih.gov/24603571
https://pubmed.ncbi.nlm.nih.gov/24603571
Autor:
Mo Dimbil, Abril Giron, Sanjay Gandhi, Ravi Iyer, Daniel O. Claassen, Keith B. Hoffman, Lisa De Boer
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 87:A73.2-A73
Background In clinical trials of patients with Huntington’s disease (HD), treatment with TBZ resulted in more neuropsychiatric AEs compared to placebo, including insomnia, somnolence, anxiety, depression, and agitation. Aim To summarise post-market
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::87d60fcd24266dc4b2dc705c75a83762
https://doi.org/10.1136/jnnp-2016-314597.206
https://doi.org/10.1136/jnnp-2016-314597.206