by the FDA*1-6
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In clinical trials for stroke prevention in AF, Pradaxa 150 mg BID remains the only NOAC to significantly reduce rates of ischemic stroke compared with warfarin in its respective study (RE-LY©)†‡§1–5
Protection through a proven safety profile1–5
Over 5 years of real-world experience6–10
Protection and treatment for 7 approved uses1
*In the USA, the licensed doses for Pradaxa are 150 mg BID and 75 mg BID for the prevention of stroke and systemic embolism in adult patients with non-valvular AF.
†Relative risk reduction.
‡The above data is taken from the pivotal RE-LY trial where the primary endpoint was stroke or systemic embolism.11
§Pradaxa 110 mg twice daily, indicated for certain patients, was shown to be as effective as warfarin in preventing stroke or systemic embolism. These results were shown in the RE-LY trial, which was a PROBE (prospective, randomized, open-label with blinded endpoint) evaluation trial.11