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Description
MATSUSAKA, T., FUJII, M., NAKANO, T., TERAI., T., KURATA, A., IMAIZUMI, M., & ABE, H
The dose ranges studied spanned from 0.25 mg to 54 mg, allowing for assessment of dose-response relationships in adverse effect profiles
Generally well tolerated with a low incidence of side effects at typical doses [3]
Conclusion: In this real-world nation-wide observational study, DOACs were initiated within four days in the majority of the patients
