Insulin Detemir
Appearance
Insulin detemir
Levemir, Levemir FlexTouch (US discontinuation announced 2024)
Experience
No personal reports yet
No clinical reports yet
Log in to add your own experience.
Problems
No problems yet. Be the first to suggest one.
+ Add a problemTitration strategies
No titration strategies yet. Be the first to suggest one.
Effects
No effects listed yet. Be the first to suggest one.
Relevant anecdote
No anecdotes yet. Share a relevant one.
Relevant Literature
No literature entries yet.
Log in to submit relevant literature.
Summary
Common uses
Type 1 diabetes mellitus0, Type 2 diabetes basal coverage0
Pharmacy
Starting dose
~10 units SC at the same time daily, or 0.1-0.2 units/kg/d; titrate by fasting glucose. Frequently dosed BID at moderate-to-high doses
Preparations
100 U/mL FlexTouch pen, vial
US FDA Max
Titrated to glucose
Pharmacology
Routes
Subcutaneous
Onset
1-2 hours
Duration
~12-24 hours (dose-dependent; BID dosing often needed at higher doses)
Half-life
~7 hours apparent[1]
Bioavailability
~60% from subcutaneous depot (reduced by reversible albumin binding via the myristic acid side chain that also extends duration)[1]
Pregnancy
One of the better-studied basal insulin analogs in pregnancy; reassuring data.[citation needed]
Legal status
Rx-only in US
Purported mechanism
Insulin detemir has a 14-carbon myristic fatty acid attached to LysB29 that binds reversibly to plasma and tissue albumin; the slow albumin dissociation prolongs the apparent half-life and produces a less peaked basal profile than NPH.0 Generally associated with less weight gain than glargine, possibly via central appetite effects. Novo Nordisk announced US discontinuation in 2024 as part of basal-insulin portfolio rationalization (degludec, glargine biosimilars remain)[1].
References
- ↑ 1.0 1.1 1.2 FDA Prescribing Information, Levemir (insulin detemir), Novo Nordisk, current revision. https://www.accessdata.fda.gov/drugsatfda_docs/label/2017/021536s060lbl.pdf