This observational study is conducted in Africa. The aim of this observational study is to evaluate the efficacy and the incidence of serious adverse drug reactions while using insulin Levemir® under normal clinical practice conditions.
Study Type
OBSERVATIONAL
Enrollment
798
Start dose and frequency to be prescribed by the physician as a result of the normal clinical evaluation
Unnamed facility
Casablanca, Morocco
The incidence of serious adverse drug reactions, including major hypoglycaemic events
Time frame: From baseline to 12 and 24 weeks of Levemir® therapy, respectively
Number of serious adverse events
Time frame: From baseline to 12 and 24 weeks of Levemir® therapy, respectively
Number of all adverse events
Time frame: From baseline to 12 and 24 weeks of Levemir® therapy, respectively
Number of all hypoglycaemic events
Time frame: in the 4 weeks preceding the visits at 12 weeks and 24 weeks.
Weight changes
Time frame: at the end of study
HbA1c
Time frame: at the end of study
Sub -group analysis of hypo risk
Time frame: From baseline to 12 and 24 weeks of Levemir® therapy, respectively
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.