Hypertension
Conditions
Sponsors
TAKEDA PHARMACEUTICAL COMPANY LTD.
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Patients with a history of hypersensitivity to any of the ingredients of in azilsartan. 2. Patients who are pregnant or having possibilities of being pregnant
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Frequency of adverse drug reactions Primary timeframe12 months The frequencies of all adverse drug reactions observed during the observation period will be tabulated by type and seriousness. Adverse events are defined as unfavorable and unintended all of signs, symptoms or diseases temporally associated with administration of azilsartan,whether or not it was considered related to the treatment. Among these, events which are considered to have a casual relationship with azilsartan are defined as adverse drug reactions. | — |
Secondary
| Measure | Time frame |
|---|---|
| Change in blood pressure Secondary timeframeFrom baseline to 12 months Tabulation of actual measured value and changes from baseline at each test time point in blood pressure (test value at each test time point after baseline - test value at baseline) | — |
Outcome results
None listed