Ischemic and Thrombotic Events Associated with Concomitant Xa-inhibiting Direct Oral Anticoagulants and Antiepileptic Drugs: Analysis of the FDA Adverse Event Reporting System (FAERS)

Amichai Perlman; Maor Wanounou; Rachel Goldstein; Lotan Choshen Cohen; Daniel E. Singer; Mordechai Muszkat

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Ischemic and Thrombotic Events Associated with Concomitant Xa-inhibiting Direct Oral Anticoagulants and Antiepileptic Drugs: Analysis of the FDA Adverse Event Reporting System (FAERS)

机译：与伴随的XA抑制直接口服抗凝血剂和抗癫痫药物相关的缺血性和血栓形成事件：对FDA不良事件报告系统的分析（FAE）

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来源
《CNS drugs》 |2019年第12期|共6页
作者
Amichai Perlman; Maor Wanounou; Rachel Goldstein; Lotan Choshen Cohen; Daniel E. Singer; Mordechai Muszkat;
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作者单位

1grid.9619.70000 0004 1937 0538Division of Clinical Pharmacy School of Pharmacy Faculty of;

3grid.17788.310000 0001 2221 2926Department of MedicineHadassah Hebrew University HospitalP.O. Box;

1grid.9619.70000 0004 1937 0538Division of Clinical Pharmacy School of Pharmacy Faculty of;

3grid.17788.310000 0001 2221 2926Department of MedicineHadassah Hebrew University HospitalP.O. Box;

4grid.32224.350000 0004 0386 9924Division of General Internal MedicineMassachusetts General;

3grid.17788.310000 0001 2221 2926Department of MedicineHadassah Hebrew University HospitalP.O. Box;

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正文语种 eng
中图分类药学;
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1. Ischemic and Thrombotic Events Associated with Concomitant Xa-inhibiting Direct Oral Anticoagulants and Antiepileptic Drugs: Analysis of the FDA Adverse Event Reporting System (FAERS) [J] . Amichai Perlman, Maor Wanounou, Rachel Goldstein, CNS drugs . 2019,第12期

机译：与伴随的XA抑制直接口服抗凝血剂和抗癫痫药物相关的缺血性和血栓形成事件：对FDA不良事件报告系统的分析（FAE）
2. Bisphosphonates and Nonhealing Femoral Fractures: Analysis of the FDA Adverse Event Reporting System (FAERS) and International Safety Efforts: A Systematic Review from the Research on Adverse Drug Events And Reports (RADAR) Project. [J] . Beatrice J Edwards, Andrew D Bunta, Joseph Lane, The Journal of Bone and Joint Surgery. American Volume . 2013,第4期

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机译：PCV46中风和血栓形成事件与伴随的直接口服抗凝血剂和抗癫痫药物在FDA不良事件报告系统中

Ischemic and Thrombotic Events Associated with Concomitant Xa-inhibiting Direct Oral Anticoagulants and Antiepileptic Drugs: Analysis of the FDA Adverse Event Reporting System (FAERS)

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