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This study will be a retrospective observational study assessing identifiable tolerability problems in terms of their comparative incidence among Human Immunodeficiency Virus (HIV) patients treated with cART regimens including one of four different protease inhibitors [Atazanavir sulfate (ATV), Darunavir (DRV), Fosamprenavir (FPV), or Lopinavir (LPV)] and the impact of these identifiable tolerability problems on PI persistence, healthcare utilization, and healthcare costs.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Atazanavir | HIV patients on antiretroviral therapy using Atazanavir | ||
| Darunavir | HIV patients on antiretroviral therapy using Darunavir | ||
| Fosamprenavir | HIV patients on antiretroviral therapy using Fosamprenavir | ||
| Lopinavir | HIV patients on antiretroviral therapy using Lopinavir |
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| Measure | Description | Time Frame |
|---|---|---|
| Percent of patients.with new onset GI symptoms after initiating an ATV, DRV, FPV, or LPV containing combination antiretroviral therapy (cART) regimen | 6 months |
| Measure | Description | Time Frame |
|---|---|---|
| Percent of patients with new onset lipid abnormalities or new onset jaundice (separately) after initiating an ATV, DRV, FPV, or LPV containing combination antiretroviral therapy (cART) regimen | 6 months | |
| Healthcare utilization | 6 months |
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Inclusion Criteria:
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Employees and dependents with employer-based health insurance coverage
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| Name | Affiliation | Role |
|---|---|---|
| Bristol-Myers Squibb | Bristol-Myers Squibb | Study Director |
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| Label | URL |
|---|---|
| BMS Clinical Trials Disclosure | View source |
| For FDA Safety Alerts and Recalls refer to the following link: | View source |
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| Healthcare costs | 6 months |