This study is conducted in Asia. The aim of this observational study is to investigate the clinical safety profile and effectiveness while using SC NovoRapid™ (insulin aspart) in patients with coexisting diabetes and kidney disease under normal clinical practice conditions in India.
Study Type
OBSERVATIONAL
Safety and effectiveness data collection in connection with the use of the drug NovoRapid™ in patients with coexisting diabetes and chronic kidney disease in daily clinical practice.
Incidence of major hypoglycaemic episodes
Time frame: during 26 weeks
Number of serious adverse events
Time frame: during 26 weeks
Number of serious adverse drug reactions
Time frame: during 26 weeks
Number of all daytime and nocturnal major hypoglycaemic events
Time frame: during 26 weeks
Number of major hypoglycaemic events related to omission of a meal after injection
Time frame: during 26 weeks
Number of all minor (daytime and nocturnal) hypoglycaemic events
Time frame: during 4 weeks proceeding each study visits during Insulin Aspart (NovoRapidTM) therapy
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