Reporting of Adverse Events in Patients Treated With New Oral Anticoagulants

Hvidovre University Hospital20 enrolled

Overview

Serious adverse events in patients treated with new oral anticoagulants are underreported.

The study investigates if serious adverse events in patients treated with NOAC are reported to the Health and Medicines Authority.

Study Type

OBSERVATIONAL

Enrollment

Sex: ALL

Medical Language ↔ Plain English

Inclusion Criteria: * patients admitted for GI bleeding while in treatment with NOAC Exclusion Criteria: * none

Hvidovre Hospital University of Copenhagen

Hvidovre, Denmark

Proportion of patients admitted with adverse event reported to authorities

Time frame: Within one year of admission

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