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This is a non-interventional study of remazolam toluenesulfonate (rebenin ®) for injection in Chinese patients. A total of 1000 patients were enrolled in this study based on the preliminary safety assessment of rebenin ®, and all safety information was obtained
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| General anesthesia cohort |
| ||
| Bronchoscopy sedation cohort |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Remimazolam Tosilate for Injection | Drug | Remimazolam Tosilate for Injection |
|
| Measure | Description | Time Frame |
|---|---|---|
| Adverse events | Use adverse event record form,Refer to version 5.0 of the NCI-CTCAE | Within 3 days of receiving General anesthesia and bronchoscopy sedation |
| Measure | Description | Time Frame |
|---|---|---|
| Serious adverse events | Refer to SAE definition standards | Within 3 days of receiving General anesthesia and bronchoscopy sedation |
| Adverse drug reactions | By evaluating the association of adverse events with drugs |
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Inclusion Criteria:
Exclusion Criteria:
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All patients receiving remazolam toluenesulfonate for general anesthesia or bronchoscopy sedation
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Xiangya Hospital of Central South University | Changsha | Hunan | 410008 | China |
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| Within 3 days of receiving General anesthesia and bronchoscopy sedation |
| Injection pain | Refer to the NCI-CTCAE <5.0> grading criteria for drug injection site reactions | Within 3 days of receiving General anesthesia and bronchoscopy sedation |
| ID | Term |
|---|---|
| D007267 | Injections |
| ID | Term |
|---|---|
| D004333 | Drug Administration Routes |
| D004358 | Drug Therapy |
| D013812 | Therapeutics |
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