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Ondexxya for Intravenous Injection 200mg Drug Use Result Investigation (All Case Investigation)
Sponsor: AstraZeneca
Summary
This survey will be conducted to investigate the status of occurrence of the safety specifications set for "Safety specification" in patients who received Ondexxya Intravenous Injection 200 mg. In addition, this survey will be implemented to understand the followings by collecting safety and effectiveness information under actual use conditions.
Key Details
Gender
All
Age Range
Any - Any
Study Type
OBSERVATIONAL
Enrollment
300
Start Date
2022-06-02
Completion Date
2026-08-31
Last Updated
2026-03-10
Healthy Volunteers
No
Locations (72)
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Aichi, Japan
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Aichi, Japan
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Aichi, Japan
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Akita, Japan
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Aomori, Japan
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Chiba, Japan
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Chiba, Japan
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Chiba, Japan
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Ehime, Japan
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Ehime, Japan
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Fukui, Japan
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Fukui, Japan
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Fukuoka, Japan
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Fukuoka, Japan
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Fukushima, Japan
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Gifu, Japan
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Gifu, Japan
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Gunma, Japan
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Gunma, Japan
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Gunma, Japan
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Hiroshima, Japan
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Hokkaido, Japan
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Hokkaido, Japan
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Hyōgo, Japan
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Hyōgo, Japan
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Ibaraki, Japan
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Ishikawa, Japan
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Kagawa, Japan
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Kagoshima, Japan
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Kanagawa, Japan
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Kanagawa, Japan
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Kochi, Japan
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Kumamoto, Japan
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Kumamoto, Japan
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Kyoto, Japan
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Kyoto, Japan
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Mie, Japan
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Mie, Japan
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Miyagi, Japan
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Miyazaki, Japan
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Nagano, Japan
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Nagano, Japan
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Nagasaki, Japan
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Nagasaki, Japan
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Nara, Japan
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Niigata, Japan
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Niigata, Japan
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Numakunai, Japan
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Okayama, Japan
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Okinawa, Japan
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Osaka, Japan
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Osaka, Japan
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Saga, Japan
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Saitama, Japan
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Shiga, Japan
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Shiga, Japan
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Shimane, Japan
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Shizuoka, Japan
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Tochigi, Japan
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Tochigi, Japan
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Tokushima, Japan
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Tokyo, Japan
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Tokyo, Japan
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Tottori, Japan
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Toyama, Japan
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Wakayama, Japan
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Wakayama, Japan
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Yamagata, Japan
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Yamagata, Japan
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Yamaguchi, Japan
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Yamaguchi, Japan
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Yamanashi, Japan