Phase
Condition
N/ATreatment
N/AClinical Study ID
All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- All patients treated with this drug to neutralize the anticoagulant effect of a FXainhibitor (apixaban, rivaroxaban, or edoxaban) at onset of a life-threateningbleeding episode or a unarrestable bleeding episode.
Exclusion
Exclusion Criteria:
- N/A
Study Design
Study Description
Connect with a study center
Research Site
Aichi,
JapanSite Not Available
Research Site
Akita,
JapanSite Not Available
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Aomori,
JapanSite Not Available
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Chiba,
JapanSite Not Available
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Ehime,
JapanSite Not Available
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Fukui,
JapanSite Not Available
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Fukuoka,
JapanSite Not Available
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Fukushima,
JapanSite Not Available
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Gifu,
JapanSite Not Available
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Gunma,
JapanSite Not Available
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Hiroshima,
JapanSite Not Available
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Hokkaido,
JapanSite Not Available
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Hyogo,
JapanSite Not Available
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Ibaraki,
JapanSite Not Available
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Ishikawa,
JapanSite Not Available
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Iwate,
JapanSite Not Available
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Kagawa,
JapanSite Not Available
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Kagoshima,
JapanSite Not Available
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Kanagawa,
JapanSite Not Available
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Kochi,
JapanSite Not Available
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Kumamoto,
JapanSite Not Available
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Kyoto,
JapanSite Not Available
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Mie,
JapanSite Not Available
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Miyagi,
JapanActive - Recruiting
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Miyazaki,
JapanSite Not Available
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Nagano,
JapanSite Not Available
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Nagasaki,
JapanSite Not Available
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Nara,
JapanSite Not Available
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Niigata,
JapanSite Not Available
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Okayama,
JapanSite Not Available
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Okinawa,
JapanSite Not Available
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Osaka,
JapanSite Not Available
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Saga,
JapanSite Not Available
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Saitama,
JapanSite Not Available
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Shiga,
JapanSite Not Available
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Shimane,
JapanSite Not Available
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Shizuoka,
JapanSite Not Available
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Tochigi,
JapanSite Not Available
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Tokushima,
JapanSite Not Available
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Tokyo,
JapanSite Not Available
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Tottori,
JapanSite Not Available
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Toyama,
JapanSite Not Available
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Wakayama,
JapanSite Not Available
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Yamagata,
JapanSite Not Available
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Yamaguchi,
JapanActive - Recruiting
Research Site
Yamanashi,
JapanSite Not Available
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