Drug lookup
Drug reference

inamrinone

PDE3 inhibitor (positive inotrope / vasodilator) · inotropic agent

START
Load 0.75 mg/kg IV slow, then 5–10 mcg/kg/min infusion
TYPICAL MAX
10 mg/kg/24 h
STOP IF
Severe thrombocytopenia, ventricular arrhythmia, or severe hypotension
WATCH
ECG, BP/CO, platelets, LFTs; short-term use only
CDSCO approvedATC C01CE01
Dose laddermg/d
0.75mg/kg load5mcg/kg/min10high inf
Renal dose adjustmenteGFR mL/min/1.73m²
CAUTIONStandard titration30REDUCEReduce infusion / extend; monitor le…90

KDIGO 2024 + manufacturer label

Pharmacokineticsplasma · t hours
3minONSET12minPEAK3.6h1hDURATION
ONSET
3min · IV onset
PEAK
12min · steady state
3.6h ·
DURATION
1h · post-stop
EXCRETION
Renal — mainly metabolites
route + CYP
INTERACTIONS
1 major
SEVERE in our sources
PREGNANCY
Use only if benefit outweighs risk; limited data.
FDA category + note
Top interactionssee all 5
  • Other Pde3 InhibitorsSevereDatabaseKimi deep-research + Cla

Mechanism

Inhibits cardiac and vascular phosphodiesterase-3, raising intracellular cAMP — increases myocardial contractility (positive inotropy) and produces vasodilation (afterload/preload reduction); inodilator profile useful in heart failure.

Indications

Short-term IV management of severe heart failure unresponsive to other therapy

Dosing

Adult
Loading 0.75 mg/kg IV slowly over 2–3 min, then maintenance 5–10 mcg/kg/min IV infusion; max ~10 mg/kg/24 h.
Pediatric
Specialist (neonates/infants weight-based).
Renal adjustment
Caution; reduce infusion rate / extend interval in severe impairment.
Hepatic adjustment
Caution in significant impairment.
Geriatric
Standard ICU titration; monitor BP/arrhythmias.
Max dose
10 mg/kg/24 h

Pharmacokinetics

Onset
Within 2–5 min (IV)
Peak effect
~10 min (steady-state infusion)
Duration
30–60 min after stopping infusion
Half-life
~3.6 h (longer in heart failure / renal failure)
Bioavailability
IV 100%
Protein binding
~10–49%
Metabolism
Hepatic
Excretion
Renal (mainly metabolites)

Contraindications

  • Hypersensitivity to bisulfites (formulation contains sodium metabisulphite)
  • Severe aortic / pulmonic valvular disease (caution)
  • Acute MI in some scenarios

Side effects

Common
Thrombocytopenia (especially prolonged use)ArrhythmiaHypotensionNausea/vomitingHeadache
Serious
  • Severe thrombocytopenia
  • Ventricular arrhythmias
  • Severe hypotension
  • Hepatotoxicity (prolonged use)
  • Anaphylactoid reactions

Pregnancy & lactation

Pregnancy

Use only if benefit outweighs risk; limited data.

Lactation

Limited data; avoid.

Drug interactions

Other Pde3 Inhibitors
Severe
Database

Duplicate therapy

Do not combine

Source: Kimi deep-research + Cla

Catecholamines
Moderate
Database

Additive inotropy

Titrate carefully

Source: Kimi deep-research + Cla

Disopyramide
Moderate
Database

Additive hypotension (combined positive inotropic/vasodilator)

Monitor BP closely

Source: Kimi deep-research + Cla

Diuretics
Moderate
Database

Additive hypotension / hypokalaemia

Monitor K and BP

Source: Kimi deep-research + Cla

Digoxin
Mild
Database

Possible additive inotropy / arrhythmia

Monitor ECG

Source: Kimi deep-research + Cla

Related guidelines

Ask House about inamrinone

Continue into a citation-backed clinical answer with the drug context already attached.

Sources: KD Tripathi 7e·Verified: 2026-05-20 · House clinical team·Cockpit curated: 2026-05-20