Rapid-acting insulin analogueNARROW THERAPEUTIC INDEXREQUIRES MONITORING

Insulin aspart

NovoRapid · Fiasp · Insulin aspart Sanofi · Kirsty

The mealtime insulin in Swedish healthcare and simultaneously the insulin used for intravenous infusion in diabetic ketoacidosis and hyperosmolar hyperglycaemic state. Subcutaneously it has an onset within 10–20 minutes and a duration of 3–5 hours; intravenously the half-life is a few minutes, which makes the infusion fully controllable but also means the effect ceases within minutes if the drip stops. Always clearly distinguish the subcutaneous from the intravenous regimen — they have no dose relationship.

BOXED WARNING

Hypoglycaemia is the dose-dependent toxicity and can be life-threatening. The unit abbreviation must never be written as U or IE in handwritten prescriptions — misinterpretation produces a tenfold overdose. During intravenous infusion in ketoacidosis, plasma potassium must be known and at least 3,3 mmol/l before insulin is started; insulin drives potassium intracellularly and can trigger life-threatening hypokalaemia with arrhythmia.

Dosing in adults

By indicationuppdaterad 2026-08-22
IndicationRegimenComment
Mealtime insulin, subcutaneousTotal daily dose 0,3–0,5 units/kg at initiation, of which approximately half as mealtime doses distributed across breakfast, lunch, and dinnergiven 0–10 minutes before the meal (Fiasp at the start of the meal)
Correction dose, subcutaneous(current plasma glucose − target) divided by the insulin sensitivity factor, where the factor ≈ 100 divided by total daily doseat least 3 hours between corrections, otherwise the effects stack
Diabetic ketoacidosis, intravenous50 units in 50 ml sodium chloride 9 mg/ml (1 unit/ml) in a syringe, infusion 0,1 units/kg/hour without boluspotassium ≥ 3,3 mmol/l first; glucose 100 mg/ml 75–125 ml/hour when plasma glucose < 12–15 mmol/l
Hyperosmolar hyperglycaemic stateFluids first; insulin infusion 0,05 units/kg/hour when plasma glucose has stopped falling on fluids alonelower plasma glucose and osmolality slowly, at most 3–4 mmol/l per hour
Acute hyperkalaemia10 units iv together with 25 g glucose (e.g. 50 ml glucose 500 mg/ml)check plasma glucose after 30 and 60 minutes
Renal impairment

Insulin requirements fall when eGFR drops below 60 ml/min and markedly below 30 ml/min — insulin is partly eliminated renally. No fixed percentage; reduce the dose stepwise and increase glucose monitoring frequency. Remains usable in dialysis.

Hepatic impairment

Insulin requirements are unpredictable: reduced gluconeogenesis and depleted glycogen stores lower requirements, while insulin resistance in steatosis raises them. No fixed dose adjustment — titrate against measurements.

Children

Same weight-based principles as in adults. In ketoacidosis in children, insulin infusion is 0,05–0,1 units/kg/hour and never as a bolus, and fluids are given more slowly because of the risk of cerebral oedema — follow the paediatric unit protocol.

Pitfall

Do not give the subcutaneous mealtime dose as a substitute for insulin infusion in ketoacidosis — absorption is unreliable in the dehydrated and peripherally cold patient. The most common serious mistake is the reverse: stopping the infusion when ketoacidosis has resolved without giving subcutaneous basal insulin at least one hour before, causing the patient to re-ketose within a few hours.

Pharmacokinetics

ONSET (SC)
10–20 minutes
PEAK EFFECT (SC)
1–3 hours
DURATION (SC)
3–5 hours
t½ (SC)
approximately 1,5 hours
t½ (IV)
a few minutes
DEGRADATION
Insulin receptor-mediated in liver, kidney, and muscle
EXCRETION
Renal (peptide fragments)
STRENGTH
100 units/ml

Adverse effects by frequency

≥ 10 %
Hypoglycaemia, injection site reaction, weight gain
1–10 %
Lipohypertrophy, pruritus and erythema at the injection site, transient refractive disturbance with rapid glucose reduction
< 1 %
Severe hypoglycaemia with loss of consciousness and seizures, hypokalaemia with arrhythmia, anaphylaxis, oedema