Source: FDA label
| Molecular formula | C267H402N64O76S6 |
|---|---|
| Molecular weight | 5917 g/mol |
| Registered trials | 240 |
| PubChem CID | 16137271 |
| Drug class | Insulin Analog [EPC] |
| Brand names | Levemir |
Mechanism of Action
Managing blood glucose day to day is the central challenge of living with diabetes, and long-acting insulins like insulin detemir are built for that steady, background role. This monograph covers what it is, what it is approved for, and what the safety data show.
Key takeaways
- Insulin detemir is a long-acting human insulin analog sold as Levemir.
- It is approved to improve glycemic control in adults and children with diabetes mellitus.
- It is not recommended for treating diabetic ketoacidosis.
- Over 240 registered trials have studied this compound, including comparisons with other basal insulins.
- Reported reactions in safety databases are dominated by glucose swings and gastrointestinal symptoms.
What Insulin Detemir Is
Insulin detemir belongs to the insulin analog drug class. Like natural insulin, it lowers blood glucose by helping muscle and fat tissue take up glucose from the blood while telling the liver to slow its own glucose production. It also curbs the breakdown of fat and protein and supports protein synthesis. Its large, complex structure (molecular formula C267H402N64O76S6) reflects its design as a modified, long-acting version of the insulin molecule.
What Insulin Detemir Is Approved For
Levemir is approved to improve glycemic control in both adult and pediatric patients with diabetes mellitus. The label specifically notes it is not recommended for treating diabetic ketoacidosis. No boxed warning appears on the label.
What The Evidence Shows
More than 240 trials have been registered studying insulin detemir. A completed Phase 3 trial compared insulin degludec to insulin detemir, both given alongside insulin aspart, in pregnant women with type 1 diabetes. A separate, non-phase study looked at insulin detemir specifically in the context of obesity management, and that trial remains active but not recruiting.
Reported Side Effects
Reports submitted to safety databases most often describe changes in blood glucose itself, with increased blood glucose (6,237 reports) far outnumbering decreased blood glucose (1,579). Gastrointestinal symptoms are also common, led by nausea (2,019), diarrhoea (1,422), and vomiting (1,361). Fatigue (1,564) and dyspnoea (1,301) appear as well, along with reports of the drug being ineffective (1,372). These figures reflect submitted report counts, not confirmed rates of incidence or proof that the drug caused the reaction.
FAQ
Sources: FDA label (DailyMed) for Levemir ClinicalTrials.gov registry FDA Adverse Event Reporting System (FAERS) PubChem CID 16137271
Updated 2026-08-04