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Insulin

Insulin (Soluble / Actrapid)

Brand names: Actrapid, Humulin S, NovoRapid (aspart), Novorapid

Used in: Diabetes & DKA Hyperkalaemia

Soluble (regular) human insulin, a short-acting insulin given subcutaneously for diabetes and intravenously in acute settings such as diabetic ketoacidosis and hyperkalaemia.

Dosing — being independently re-sourced

ClinCalc Pro is rebuilding its dose data from primary open sources — the manufacturer SmPC (eMC), the WHO Model Formulary and other official references — under clinician review. This drug's structured dose is not yet published here. Confirm all doses against the product SmPC and your local formulary before prescribing.

Clinical monograph

How it works

Soluble insulin replaces endogenous insulin, promoting cellular glucose uptake, suppressing hepatic glucose output, and driving potassium into cells; given subcutaneously it has a slower onset and longer duration than rapid-acting analogues.

Prescribing in practice

  • The most important safety point is the risk of hypoglycaemia, compounded by insulin being a high-alert medicine prone to prescribing and administration errors, so use insulin-specific syringes and never abbreviate units as 'U'.
  • When given subcutaneously before meals, allow an adequate interval between injection and eating because onset is slower than analogue insulins.
  • Intravenous variable-rate infusions require close glucose and potassium monitoring with a clear protocol.

Monitoring

Monitor capillary or laboratory blood glucose, and potassium when given intravenously, adjusting the regimen to avoid hypoglycaemia.

Counselling the patient

  • Recognise and treat hypoglycaemia promptly and always carry a fast-acting source of sugar.
  • Inject a short time before meals as advised, and rotate injection sites to avoid lipohypertrophy.
  • Never change insulin type or strength without specialist advice.

Evidence & guidelines

Insulin is identified by the MHRA/NHS as a high-alert medicine, and intensive glycaemic control with insulin reduced complications in landmark trials such as DCCT and UKPDS.

Reference: JBDS DKA Guidelines 2023; NICE NG17; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. Monograph status: clinician-reviewed (2026-07-04).

Related

Curated clinical cross-links plus same-class fallbacks.