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New Drug Update 2010-2011 Faculty Disclaimer - CME Conferences

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2 nd Annual Essentials in Primary Care<br />

Fall Conference<br />

Friday, November 11, <strong>2011</strong><br />

Dabigatran- Pradaxa<br />

• DOSING: Recommended Dose for patients with creatinine<br />

clearance (CrCl) >30 mL/min, the recommended dose of<br />

dabigatran is 150 mg taken orally, twice daily, with or without<br />

food. For patients with CrCl 15-30 mL/min, or patients 75 years<br />

of age or older the recommended dose is 75 mg twice daily<br />

•<br />

– Instruct patients to swallow the capsules whole. Breaking,<br />

chewing, or emptying the contents of the capsule can result<br />

in increased exposure.<br />

– Pradaxa capsules will hydrolyze over time when exposed to<br />

humidity, causing a breakdown of active ingredient, and<br />

rendering the medication less effective. Pradaxa is<br />

packaged in a 30-day supply bottle with a desiccant cap or<br />

in unit-of-use blister packaging to minimize product<br />

breakdown from moisture.<br />

Rivaroxaban – Xarelto<br />

by Bayer HealthCare AG and Janssen Pharmaceuticals<br />

Rivaroxaban exhibits a linear pharmacokinetic<br />

relationship with a rapid onset of action, resulting<br />

in maximal factor Xa inhibition in approximately 3<br />

hours. Maintenance of the anti–factor Xa effect<br />

lasted 8 to 12 hours, depending on the dose of<br />

rivaroxaban.<br />

Terminal half-life of rivaroxaban is approximately 9<br />

hours in adults and 12 hours in elderly patients<br />

(older than 65 years of age). Elimination of<br />

rivaroxaban occurs by multiple routes: renal (onethird<br />

is excreted unchanged), biliary/fecal, and<br />

hepatic (through CYP-450 3A4). Renal function<br />

impairment may influence elevated plasma<br />

concentrations and increased anti-Xa activity;<br />

therefore, dose adjustments may be required<br />

Wayne Weart<br />

<strong>New</strong> <strong>Drug</strong> <strong>Update</strong> Part I

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