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Calcium Sensitiser / Inodilator

Levosimendan

Brand names: Simdax

Levosimendan is a calcium-sensitising inotrope and vasodilator given by intravenous infusion, used in specialist settings for acute decompensated heart failure with low cardiac output.

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

It enhances myocardial contractility by sensitising cardiac troponin C to calcium without raising intracellular calcium, and opens vascular ATP-sensitive potassium channels to produce arterial and venous vasodilatation; an active metabolite prolongs its haemodynamic effect.

Prescribing in practice

  • Can cause significant hypotension and tachyarrhythmias, so it should be given only with continuous cardiac and blood-pressure monitoring and is generally avoided in marked hypotension or severe outflow obstruction.
  • The long-acting active metabolite means haemodynamic and electrophysiological effects may persist for days after the infusion is stopped.
  • Correct hypovolaemia and significant electrolyte disturbance before and during the infusion, and consult the SPC for administration details.

Monitoring

Monitor blood pressure, heart rate and rhythm continuously, alongside serum potassium and other electrolytes, during and after the infusion.

Counselling the patient

  • Explain to the patient that this medicine is given as a drip in hospital under close monitoring.
  • Advise the team that low blood pressure and palpitations are recognised effects and may persist after the infusion ends.

Evidence & guidelines

Levosimendan has been evaluated in randomised trials of acute decompensated heart failure (including the SURVIVE and REVIVE studies); refer to current prescribing references for licensed indications.

Reference: RUSSLAN Trial 2002; SURVIVE Trial (Mebazaa et al, JAMA 2007); 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.