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Marsha E. Reichman

Researcher at Center for Drug Evaluation and Research

Publications -  26
Citations -  2250

Marsha E. Reichman is an academic researcher from Center for Drug Evaluation and Research. The author has contributed to research in topics: Warfarin & Dabigatran. The author has an hindex of 16, co-authored 26 publications receiving 2009 citations. Previous affiliations of Marsha E. Reichman include Food and Drug Administration.

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Cardiovascular, Bleeding, and Mortality Risks in Elderly Medicare Patients Treated With Dabigatran or Warfarin for Nonvalvular Atrial Fibrillation

TL;DR: In general practice settings, dabigatran was associated with reduced risk of ischemic stroke, intracranial hemorrhage, and death and increased risk of major gastrointestinal hemorrhage compared with warfarin in elderly patients with nonvalvular atrial fibrillation.
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Dabigatran and postmarketing reports of bleeding.

TL;DR: The FDA used the Mini-Sentinel database to determine that the actual rates of bleeding events were not higher with dabigatran than with warfarin.
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Stroke, Bleeding, and Mortality Risks in Elderly Medicare Beneficiaries Treated With Dabigatran or Rivaroxaban for Nonvalvular Atrial Fibrillation

TL;DR: Treatment with rivaroxaban 20 mg once daily was associated with statistically significant increases in ICH and major extracranial bleeding, including major gastrointestinal bleeding, compared with dabigatran 150 mg twice daily, which indicated increased risk of stroke, bleeding, and mortality in patients with nonvalvular atrial fibrillation.
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Comparative Risk for Angioedema Associated With the Use of Drugs That Target the Renin-Angiotensin-Aldosterone System

TL;DR: Compared with β-blockers, ACEIs or aliskiren was associated with an approximately 3-fold higher risk for angioedema, although the number of exposed events for aliskirens was small.
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Comparative Risk of Anaphylactic Reactions Associated With Intravenous Iron Products

TL;DR: Among patients in the US Medicare nondialysis population with first exposure to IV iron, the risk of anaphylaxis was highest for iron dextran and lowest for iron sucrose, and the risk following total iron repletion of 1000 mg administered within a 12-week period was highest.