Tiapride

Tiapride

Mechanism of action

Antipsychotic (benzamide derivative).

Antagonist of dopamine D2 and D3 receptors.

Indications and dose

Contraindications

Prolactinoma

Pheochromocytoma

Concomitant use of dopaminergic drugs (e.g. levodopa)

Side-effects

Hyperprolactinaemia

Insomnia

Fatigue

Vertigo

Neuroleptic malignant syndrome

Prolonged QT interval

Precautions

Avoid in patients with Parkinson’s disease.

Cautious use in patients with breast cancer due to effects of tiapride on prolactin levels.

Pharmacokinetics

Routes: Oral, Intravenous, Intramuscular (preferred parenteral route)

Onset of action: 30 minutes (intramuscular); 1 hour (oral)

Bioavailability: 75%

Metabolism: Minimal

Half-life of elimination: 3 hours

Excretion: Urine

Directions for administration

Tablets may be crushed.

Dilute in water for injections.

Medicinal forms

Tablet - 100 mg

1 drop = 5 mg

Solution for injection - 1 vial = 2 ml (100 mg)

References

  1. https://en.wikipedia.org/wiki/Tiapride
  2. https://www.sukl.eu/modules/medication/download.php?file=SPC190960.pdf&type=spc&as=tiapridal-spc