This post-marketing surveillance study was designed to supplement under conditions of normal clinical practice the data on the safety, tolerability and efficacy of Micardis® collected during the clinical studies.
Study Type
OBSERVATIONAL
Enrollment
19,870
Indicence of ulcera
Time frame: Up to 6 months after start of study
Incidence of gastrointestinal (GI) bleedings
Time frame: Up to 6 months after start of study
Incidence of adverse events (GI-complaints inclusive)
Time frame: Up to 6 months after start of study
Change from baseline in office blood pressure
Time frame: Up to 6 months after start of study
Response rate
full response: reduction of diastolic blood pressure (DBP) by \>= 10 mmHg or final DBP \<= 90 mmHg overall response: reduction of DBP by \>= 7mmHg or final DBP \<= 90 mmHg
Time frame: Up to 6 months after start of study
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