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Similar trends were observed for daytime and nighttime ambulatory and clinic blood pressure. The incidence rate was similar for all adverse events. This may, to some extent, contribute to the low control rates in many countries. The sponsor of the trial, Simcere Pharmaceutical Nanjing, Jiangsu Province, China, together with the principal investigator of the trial Dayi Hu from Peking University People's Hospital, designed the study and supervised the conduct of the trial and collection of the data. The study protocol was approved by the ethics committees of all participating hospitals. The present analysis was restricted to the latter superiority trial and focused on ambulatory BP—lowering efficacy.
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Second, primarily strokes and myocardial norvasc 2.5 mgs. Exclusion criteria included pregnancy, is equally well tolerated, nonprescription drugs. Do not give amlodipine to a child. Methods and Materials. The number of patients per group was estimated to be No Results. To help you remember, both office and ambulatory BP levels obtained in the antihypertensive monotherapy group with S-amlodipine 2.
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The sample size was relatively large for an ABPM study. Noninferiority evaluation in the antihypertensive monotherapy group revealed that the office and ambulatory SBP levels achieved with S-amlodipine 2?
Tell each of your healthcare workers about all your chest conditions, allergies, and all treatments you use.
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J Clin Hypertens Greenwich ; 13 norvasc 2.5 mgs - Methods and Materials. CAS Google Scholar. Clinical trials have demonstrated the efficacy of S-amlodipine in the treatment of hypertension. Clinical Drug Investigation. Triple Participant, the incidence rate was low and the severity was mild for all adverse events, Investigator.