Page 46 - Diamicron MR MIG Cycle 2(20-21) Final
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Visual Aids Page 4
                                    Diamicron MR 60 (Metformin Uncontrolled Patients)


               Page 4: Very Low Risk of Hypoglycemia:

               Moreover, with  Diamicron MR 60  you can provide such excellent  efficacy without  compromising  patients’
               safety.

               In diabetes patients on fasting who has very high risk for hypoglycemia, you can find that rate of hypoglycemia
               is very less (2.2%) with Diamicron MR 60 even count on symptomatic episodes. But in your patients at daily
               practice, Diamicron MR 60 has very low rate (0.3%) of symptomatic hypoglycemia


               By choosing Diamicron MR 60, you can regain your control at 7% from the 1st day with no compromise on safety.


               Objective

               To convince the doctors that Diamicron MR 60 has very low rate of Hypoglycemia even in fasting
               patients who have very high risk for Hypoglycemia and patients at daily clinical practice.


               Comments
               Diamicron MR provide excellent efficacy together with remarkable safety and it is very important to
               differentiate Diamicron MR from other OADs.


                                                     DIA-RAMANDAN
               Key End Points

                 Primary End points: Proportion of patients with at least 1 symptomatic hypoglycemic event.
                 Secondary End points
                   1.  Change of HbA1c level, fasting plasma glucose (FPG), and weight between inclusion and end
                       of the study
                   2.  Proportion of patients with at least 1 confirmed hypoglycemia event
                   3.  Proportion of patients with at least 1 severe hypoglycemia event
               Methodology
               DIA-RAMADAN was a real-world, prospective, international, multicenter study including adult
               patients with T2D with controlled or suboptimally controlled HbA1C (<9%), who were already
               undergoing treatment with   breakable gliclazide MR 60 mg for at least 90 days before the start of
               the  study , and not requiring insulin treatment (Figure 1). Participants continued their T2D
               treatment according to usual practice and doctor’s recommendations. A patient diary was provided
               at the beginning of the study for collecting hypoglycemia and adverse events. All data was collected
               in eCRF and regularly monitoring during study.
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