Register / Log In

First warfarin replacement approved


Dabigatran etexilate (Pradaxa, Boehringer Ingelheim) has received FDA approval for the prevention of stroke and blood clots in patients with atrial fibrillation. It is the first replacement for warfarin to win FDA approval. Warfarin was approved in 1954.

Replacement drugs for warfarin are considered blockbusters because of the critical need, particularly as the aging population becomes more vulnerable to atrial fibrillation and other conditions that can cause blood clots. Atrial fibrillation affects more than 2 million Americans.

"Pradaxa provides a long-awaited new treatment to reduce the risk of stroke in non-valvular atrial fibrillation. In addition to offering a significant reduction of stroke compared to warfarin, Pradaxa is easy to use as it does not require blood monitoring, related dose adjustments, and has no dietary restriction. These are important considerations for both physicians and patients when discussing treatment options," according to Wa'el Hashad, vice president, Cardiovascular and Metabolics Marketing, Boehringer Ingelheim.

Dabigatran is an anticoagulant that acts by inhibiting thrombin, an enzyme in the blood that is involved in blood clotting. The safety and efficacy of the drug were studied in a clinical trial comparing dabigatran etexilate with the anticoagulant warfarin. In the trial, patients taking dabigatran had fewer strokes than those who took warfarin.

“Unlike warfarin, which requires patients to undergo periodic monitoring with blood tests, such monitoring is not necessary for Pradaxa,” said Norman Stockbridge, MD, PhD, director of the Division of Cardiovascular and Renal Products, Center for Drug Evaluation and Research, in an FDA press release.

Added David Calabrese, RPH, MHP, Clinical Editor of Drug Topics’ sister publication Formulary, “Given the significant complexities associated with warfarin therapy in patients with atrial fibrillation, dabigatran may represent a pivotal advancement in the care of individuals with this condition.

“From a managed care perspective, the employment of thoughtful and judicious clinical and pharmacoeconomic assessment will be vital toward ensuring appropriate positioning of this important new therapy, as well as others soon to follow within this therapeutic area,” said Calabrese, chief clinical officer, MedMetrics Health Partners, Worcester, Mass.

Pradaxa will be available in 75 mg and 150 mg capsules.

FDA has approved Lisdexamfetamine dimesylate (Vyvanse, Shire) capsules CII for the treatment of attention deficit hyperactivity disorder (ADHD) in adolescents aged 13 to 17 years.

A growing body of evidence links use of proton pump inhibitors to increased risk of nosocomial Clostridium difficile infection and other morbidities.

Kathleen Jaeger's appointment as executive vice president and CEO of the NCPA was announced October 25 at the association's annual Convention and Trade Expo in Philadelphia.

propofol

A growing body of data supports greater pharmacist involvement in medication safety, said speaker Deb Saine at a recent Pharmacy OneSource webinar.