The objective is to collect the safety data of idarucizumab for patients treated with dabigatran who require rapid reversal of the anticoagulant effects of dabigatran in cases of uncontrolled or life-threatening bleeding or when emergency surgery or urgent procedures are required.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
1
Fukuoka Tokushukai Medical Center
Fukuoka, Kasuga, Japan
Percentage of Subjects With Drug-related Adverse Events
Percentage of subjects with drug-related adverse events is presented
Time frame: from first drug administration until 5 days after last drug administration, up to 6 days.
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.