Hypertension Clinical Trial
Official title:
Blopress Tablets Special Drug Use Surveillance 「Challenge - Quality Control」
The purpose of this study is to gain an understanding of the actual use of candesartan cilexetil (Blopress) in patients with hypertension, and to examine the changes in parameters such as blood pressure.
This special drug use surveillance was planned to gain an understanding of the actual use of
candesartan cilexetil in the new anti-hypertensive treatment environment where angiotensin
receptor blocker (ARB) combination drugs have become commercially available. The surveillance
also investigated the background factors of patients continuing treatment with candesartan
cilexetil and patients who switched from candesartan cilexetil to ARB combination drugs, as
well as changes in parameters such as blood pressure.
The usual adult dosage of Candesartan cilexetil is 4 to 8 mg, administered orally, once
daily. Meanwhile, treatment was to be started at 2 mg once daily in patients with renal
impairment and the dose could be increased up to 8 mg as necessary.
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