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Methods: All patients discharged alive, registered in the Swedish Stroke Register (Riksstroke) with acute ischemic stroke, atrial fibrillation, and DOAC initiated within 10 days post-stroke, not participating in TIMING during the study period (2017-2020), were identified

In fact, the FDA designated BPC-157 as a Category 2 bulk drug substance, meaning it cannot be compounded by commercial pharmaceutical companies due to insufficient safety evidence in humans