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"Sanofi-aventis is proud of its ability to bring innovative therapies to market and contribute to reducing the public health burden of atrial fibrillation.001) when compared to placebo, meeting the study's primary endpoint. Important Safety Information Multaq is contraindicated in patients with NYHA Class IV heart failure or NYHA Class II-III heart failure with a recent decompensation requiring hospitalization or referral to a specialized heart failure clinic. Hypokalemia and hypomagnesemia may occur with concomitant administration of potassium-depleting diuretics. Potassium levels should be maintained in the normal range pre and during administration. phentermine 37.5mg picture 5 million people in the United States and 4. phentermine 37.5mg picture The ANDROMEDA study, was terminated prematurely after enrolment of 627 of 1000 planned patients with congestive heart failure, in relation to excess mortality due to worsening heart failure in the dronedarone group [n=25 versus 12 (placebo), p=0. xanax from india

Food and Drug Administration (FDA) has approved Multaq (dronedarone) 400 mg Tablets. A registration dossier of Multaq is also under regulatory review by the European Medicines Agency (EMEA).sanofi-aventis. phentermine 37.5mg picture Multaq is an anti-arrhythmic indicated to reduce the risk of cardiovascular hospitalization in patients with paroxysmal or persistent atrial fibrillation (AF) or atrial flutter (AFL), with a recent episode of AF/AFL and associated cardiovascular risk factors, who are in sinus rhythm or who will be cardioverted. phentermine 37.5mg picture D. and represents one-third of hospitalizations for arrhythmia in Europe.