| Outcome Measures: |
Primary: Number of serious adverse drug reactions and major hypoglycaemic events reported as serious adverse drug reactions, at baseline, 12 weeks and 24 weeks | Secondary: Evaluate the prescribing patterns and choice of insulin analogues in routine clinical practice, at baseline, 12 weeks and 24 weeks|Change in number of hypoglycaemic events, at baseline, 12 weeks and 24 weeks|Change in HbA1c, at baseline, 12 weeks and 24 weeks|Change in FPG (Fasting Plasma Glucose), at baseline, 12 weeks and 24 weeks|Change in PPG (postprandial glucose), at baseline, 12 weeks and 24 weeks
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| Locations: |
Novo Nordisk Investigational Site, Algiers, 16035, Algeria|Novo Nordisk Investigational Site, Prov. de Buenos Aires, B1636DSU, Argentina|Novo Nordisk Investigational Site, Dhaka, 1206, Bangladesh|Novo Nordisk Investigational Site, Beijing, Beijing, 100004, China|Novo Nordisk Investigational Site, Cairo, Egypt|Novo Nordisk Investigational Site, Bangalore, 560001, India|Novo Nordisk Investigational Site, Jakarta, 12520, Indonesia|Novo Nordisk Investigational Site, Teheran, Iran, Islamic Republic of|Novo Nordisk Investigational Site, Amman, 11844, Jordan|Novo Nordisk Investigational Site, Seoul, 137-920, Korea, Republic of|Novo Nordisk Investigational Site, Tripoli, Libyan Arab Jamahiriya|Novo Nordisk Investigational Site, Selangor Darul Ehsan, Malaysia|Novo Nordisk Investigational Site, Mexico City, Mexico|Novo Nordisk Investigational Site, Casablanca, 20000, Morocco|Novo Nordisk Investigational Site, Karachi, Pakistan|Novo Nordisk Investigational Site, Manilla, 1605, Philippines|Novo Nordisk Investigational Site, Moscow, 119330, Russian Federation|Novo Nordisk Investigational Site, Riyadh, 3542, Saudi Arabia|Novo Nordisk Investigational Site, Singapore, 307684, Singapore|Novo Nordisk Investigational Site, Taipei, Taiwan|Novo Nordisk Investigational Site, Tunisia, 1053, Tunisia|Novo Nordisk Investigational Site, Istanbul, 34335, Turkey
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