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The objective of this PMS study was to monitor and assess the safety of Micardis tablets in patients with hypertension over a period of 6 years
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Patients with essential hypertension |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Telmisartan | Drug |
|
| Measure | Description | Time Frame |
|---|---|---|
| Blood pressure reduction | Up to 6 years | |
| Final assessment of efficacy on a 3-point scale | Up to 6 years | |
| Assessment of efficacy based on subject's demographics on a two-point scale | Up to 6 years | |
| Number of patients with adverse events | Up to 6 years | |
| Incidence rate of adverse events | based on demographic factors | Up to 6 years |
| Assessment of safety on a 4-point scale | based on adverse events and changes in abnormality of clinical laboratory tests | Up to 6 years |
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Inclusion Criteria:
Exclusion Criteria:
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Patients with essential hypertension and without prior Micardis experience
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| ID | Term |
|---|---|
| D006973 | Hypertension |
| ID | Term |
|---|---|
| D014652 | Vascular Diseases |
| D002318 | Cardiovascular Diseases |
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| ID | Term |
|---|---|
| D000077333 | Telmisartan |
| ID | Term |
|---|---|
| D001713 | Biphenyl Compounds |
| D001555 | Benzene Derivatives |
| D006841 | Hydrocarbons, Aromatic |
| D006844 | Hydrocarbons, Cyclic |
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| D006838 |
| Hydrocarbons |
| D009930 | Organic Chemicals |
| D001562 | Benzimidazoles |
| D006574 | Heterocyclic Compounds, 2-Ring |
| D000072471 | Heterocyclic Compounds, Fused-Ring |
| D006571 | Heterocyclic Compounds |