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Eur J Clin Pharmacol ; 80(2): 283-285, 2024 Feb.
Article in English | MEDLINE | ID: mdl-38112734

ABSTRACT

AIM: The present study investigated the risk of bleeding when antidepressants are added to antithrombotics. METHODS: Using data registered in VigiBase®, the WHO pharmacovigilance database, between 01/01/2000 and 31/12/2022, we compared the risk of reporting "serious" bleeding (Reporting Odds Ratio, ROR) with antidepressants + antithrombotics versus antithrombotics alone. RESULTS: Increased values of ROR were found for the association Serotonin Reuptake Inhibitors (SRIs) + Direct Oral Anticoagulants (DOACs) versus DOACs alone (ROR=1.49(1.17-1.89)). Similar results were found for Factor Xa inhibitors or Thrombin inhibitors. This association was also found for other antithrombotics: Vitamin K Antagonists (ROR=1.37(1.12-1.68)), Platelet Aggregation Inhibitors PAIs (ROR=1.38(1.21-1.57)) and Heparins (2.04(1.59-2.62)) but not with other antidepressants (Non-Selective Monoamine Reuptake Inhibitors, NSMRIs). CONCLUSION: The present study suggests an increased risk of "serious" bleeding when SRIs (but not NSMRIs) are associated with antithrombotics (all antithrombotics and not only DOACs).


Subject(s)
Fibrinolytic Agents , Pharmacovigilance , Humans , Fibrinolytic Agents/adverse effects , Antidepressive Agents/adverse effects , Selective Serotonin Reuptake Inhibitors/adverse effects , Hemorrhage/chemically induced , Hemorrhage/epidemiology , Anticoagulants/adverse effects
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