OKEP 16th September'16

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Full Name:
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Territory:
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Email Id:
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The objective of this study was to assess the efficacy, safety, and tolerability of pantoprazole magnesium _______ once daily for _____weeks, on the relief of reflux symptoms in gastro esophageal reflux disease (GERD) patients
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In Article I, the GERD symptom intensity was made by analyzing the group of ____ patients, amongst which ___ % were females & ___% males.
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In article I, the severity of symptoms in patients who are under study is reduced by ____% from baseline intensity, and the number of patients who experienced any adverse effect is ____%.
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In article: II, the efficacy of __________ and ______ is assed in patients with functional dyspepsia.
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In article II, the study was assessed on_____ patients, ____had outcome data that could be included in analyses.
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Analysis of the combined end point of pain and fullness showed that itopride yielded a _____ response than placebo.
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Delayed gastric emptying (GE) occurs in ____% of patients with long standing type 1 or 2 diabetes, and represents a major cause of morbidity.
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Subjects received both itopride of ___ mg and placebo t.i.d. for 7 days, with a washout of 7–14 days.
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Eiref consists of ________ &_________
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MRP of Eiref is____/capsule.