This study is conducted in Asia, Europe and North America. The aim of this observational study is to evaluate the safety of NovoPen Echo® by collecting safety information (incidence of technical complaints related to adverse reactions). Study duration: 12-18 weeks.
Study Type
OBSERVATIONAL
Enrollment
358
Prescribed insulin treatment delivered by NovoPen Echo®
Novo Nordisk Investigational Site
Mississauga, Canada
Novo Nordisk Investigational Site
Espoo, Finland
Novo Nordisk Investigational Site
Kfar Saba, Israel
Novo Nordisk Investigational Site
Malmö, Sweden
The incidence of technical complaints related to adverse reactions
Time frame: after 12-18 weeks (end of study)
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Novo Nordisk Investigational Site
Malmö, Sweden