This study is conducted in Africa. The aim of this observational study is to evaluate the incidence of serious adverse drug reactions while using insulin Levemir® under normal clinical practice conditions in Egypt.
Study Type
OBSERVATIONAL
Enrollment
3,593
Start dose and frequency to be prescribed by the physician as a result of the actual clinical evaluation
Unnamed facility
Giza, Egypt
Incidence of serious ADRs incl. major hypoglycemias
Time frame: after 24 weeks
Number of serious adverse events
Time frame: after 24 weeks
Number of all adverse events
Time frame: after 24 weeks
Weight changes
Time frame: after 24 weeks
HbA1c
Time frame: after 24 weeks
Subgroup analysis of hypoglycemias
Time frame: after 24 weeks
Number of all hypoglycemic events
Time frame: in the 4 weeks preceding the visits at 12 weeks and 24 weeks.
Variability in fasting Blood Sugar and average plasma glucose levels
Time frame: after 24 weeks
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