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Business objectives have changed.
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The primary objective of the study is to identify and describe any suspected (AEs) in all patients with NVAF treated with Apixaban, as a request of the National Center of Pharmacovigilance (CNFV) in Mexico.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| NVAF patients in Mexico treated with Apixaban | All patients with NVAF at the sentinel site for the CNFV in Mexico who received at least 1 dose of Apixaban to reduce the risk of stroke or systemic embolism during the specified 24-month study period |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Apixaban | Drug |
|
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| Measure | Description | Time Frame |
|---|---|---|
| Determine the reporting rate of on-treatment adverse events (AEs) by the treating physicians | Up to 24 month study period | |
| Identify, describe, and report any suspected AEs that occur while on treatment with Apixaban or preventing stroke and systemic embolism in patients with NVAF | Up to 24 months |
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For more information regarding BMS clinical trial participation, please visit www.BMSStudyConnect.com
Inclusion Criteria:
Exclusion Criteria:
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The sentinel site for the CNFV in Mexico
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| Name | Affiliation | Role |
|---|---|---|
| Bristol-Myers Squibb | Bristol-Myers Squibb | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Local Institution | Guadalajara | Jalisco | 442003 | Mexico | ||
| Local Institution |
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| ID | Term |
|---|---|
| C522181 | apixaban |
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| Puebla City |
| Puebla |
| 72040 |
| Mexico |