Product image of Haloperidol Crescent Pharma (Haloperidol) supplied by GNH India

Haloperidol Crescent Pharma

Active Ingredient:
Haloperidol
Origin:
EU

Haloperidol Crescent Pharma (Haloperidol)

Haloperidol Crescent Pharma is a prescription oral formulation containing the active ingredient haloperidol. It is marketed in the European Union and belongs to the butyrophenone class of antipsychotic agents. The product is supplied without a specific strength listed in the source data, and it is intended for use under medical supervision. It is prescribed for the management of several psychiatric conditions and is regulated as a prescription‑only medication.

Manufacturer / TM Owner

Crescent Pharma Limited

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Indications & Clinical Uses

Haloperidol Crescent Pharma is indicated for the treatment of several psychiatric disorders where dopamine blockade is therapeutic.

  • Schizophrenia, including acute exacerbations and maintenance therapy.
  • Acute psychotic episodes associated with mood disorders or substance use.
  • Tourette syndrome, particularly for reducing motor and vocal tics.
  • Severe agitation or aggression in hospitalized patients when rapid control is needed.
  • Adjunctive therapy for other conditions as determined by a qualified clinician.

Side Effects

Side effects of haloperidol may vary in frequency and severity; they are typically categorized as common or serious.

Common

  • Drowsiness, fatigue, or sedation.
  • Extrapyramidal symptoms such as tremor, rigidity, or akathisia.
  • Dry mouth, constipation, or blurred vision.

Serious

  • Neuroleptic malignant syndrome, a potentially life‑threatening reaction.
  • Tardive dyskinesia, characterized by involuntary movements.
  • Significant cardiac effects, including QT interval prolongation.

Precautions & Warnings

Before initiating Haloperidol Crescent Pharma, clinicians should assess patient history and monitor for specific risks associated with antipsychotic therapy.

  • Evaluate cardiovascular status, especially for QT prolongation risk.
  • Review personal or family history of movement disorders.
  • Assess liver and renal function, adjusting therapy as needed.
  • Use caution in patients with a history of seizures or electrolyte imbalance.
  • Monitor for signs of neuroleptic malignant syndrome during treatment.
  • Consider pregnancy and lactation status; safety data are limited.

Avoid Interactions

Haloperidol can interact with other medications, influencing its effectiveness or increasing adverse effects; interactions are grouped by clinical relevance.

Avoid

  • Concurrent use with other dopamine antagonists or high‑potency antipsychotics.
  • Strong CYP3A4 inhibitors such as ketoconazole or clarithromycin.

Use with caution

  • CYP3A4 inducers like carbamazepine or rifampin, which may lower haloperidol levels.
  • Medications that prolong the QT interval, including certain antiarrhythmics and fluoroquinolones.
  • Central nervous system depressants, for example benzodiazepines or opioids.

Frequently Asked Questions

Haloperidol Crescent Pharma is a prescription oral product that contains haloperidol, a butyrophenone antipsychotic. It works by antagonizing dopamine D2 receptors, thereby reducing dopaminergic neurotransmission in the brain.

It is commonly used for schizophrenia, acute psychosis, Tourette syndrome, and severe agitation that requires rapid control.

Haloperidol belongs to the butyrophenone class of antipsychotics and is listed under the ATC code N05AD01.

Common side effects include drowsiness, extrapyramidal symptoms such as tremor or rigidity, and anticholinergic effects like dry mouth, constipation, or blurred vision.

Serious reactions include neuroleptic malignant syndrome, tardive dyskinesia, and cardiac effects such as QT interval prolongation.

Clinicians should assess cardiovascular health, history of movement disorders, liver and kidney function, seizure history, electrolyte balance, and pregnancy or lactation status.

Haloperidol can prolong the QT interval on an electrocardiogram, which may increase the risk of arrhythmias in susceptible individuals.

Avoid concurrent use with other dopamine antagonists, high‑potency antipsychotics, and strong CYP3A4 inhibitors such as ketoconazole or clarithromycin.

When interacting drugs cannot be stopped, clinicians may adjust haloperidol dosage, monitor plasma levels, or increase cardiac monitoring, especially with QT‑prolonging agents.

Safety data for haloperidol in pregnancy and lactation are limited; the medication should be used only if the potential benefit justifies the potential risk to the fetus or infant.

Regular monitoring includes assessment of movement disorders, cardiac ECG for QT interval, liver and renal function tests, and observation for signs of neuroleptic malignant syndrome.

Haloperidol is a high‑potency typical antipsychotic with strong D2 antagonism, whereas many newer agents are atypical antipsychotics that also target serotonin receptors and often have a lower risk of extrapyramidal symptoms.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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