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    The other components of norvasc heart rate norvasc 2.5 norvasc maximum dose norvasc 10 mg side effects how long does it take the primary endpoint including cardiovascular death, resuscitated cardiac arrest, myocardial infarction, hospitalization for heart failure, stroke/TIA, or peripheral vascular disease did not demonstrate a significant difference between NORVASC and placebo .
    Incidence of Significant Clinical Outcomes for CAMELOT Clinical Outcomes Hospitalization for Revascularization* norvasc in pregnancy norvasc definition norvasc ingredients norvasc prescribing information norvasc *Total patients with these events Studies in Patients with Congestive Heart Failure: NORVASC has been compared to placebo in four 8-12 week studies of patients with NYHA class II/III heart failure, involving a total of 697 patients .
    In these studies, there was no evidence of worsened heart failure based on measures of exercise tolerance, NYHA classification, symptoms, or norvasc left ventricular ejection fraction .
    In a long-term (follow-up at norvasc least 6 months, mean 13 . 8 months) placebo-controlled mortality/morbidity study of NORVASC 5-10 mg in 1153 patients with NYHA classes III (n=931) or IV (n=222) heart failure on stable doses of diuretics, digoxin, and ACE NDA 19-787/S-038 inhibitors, NORVASC had no effect on the primary endpoint of the study which was the combined endpoint of all-cause mortality and cardiac morbidity (as defined by life-threatening arrhythmia, acute myocardial infarction, or hospitalization for worsened heart failure), or on NYHA classification, or symptoms of heart norvasc failure .
    Total combined all-cause mortality and cardiac morbidity events were 222/571 (39%) for patients on NORVASC and 246/583 (42%) for patients on norvasc user reviews norvasc weight loss norvasc manufacturer what is norvasc taken for norvasc placebo; the cardiac morbid events represented about 25% of the endpoints in the study .

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