Product image of Halkid (Haloperidol) supplied by GNH India

Halkid

Active Ingredient:
Haloperidol
Origin:
EU

Halkid (Haloperidol)

Halkid is a prescription medication that contains the active ingredient haloperidol, a butyrophenone antipsychotic, supplied in an oral dosage form. It is marketed in the European Union and is classified under the ATC code N05AD01. Haloperidol works as a dopamine D2 receptor antagonist and is used under medical supervision for certain psychiatric conditions. The product is intended for adult patients and should be prescribed by a healthcare professional after assessment.

Manufacturer / TM Owner

Syri Pharma Limited

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Indications & Clinical Uses

Halkid (haloperidol) is indicated for the management of several psychiatric disorders where dopamine dysregulation is implicated.

  • Schizophrenia, including acute exacerbations and maintenance therapy.
  • Acute psychotic episodes associated with mood disorders or substance use.
  • Manic episodes in bipolar disorder when rapid control of agitation is required.
  • Severe agitation or hostility in patients with dementia, when non‑pharmacologic measures are insufficient (off‑label in some regions).
  • Adjunctive treatment for Tourette syndrome or other hyperkinetic movement disorders (off‑label).

Side Effects

Haloperidol may cause a range of adverse effects that vary in frequency and severity, affecting multiple organ systems.

Common

  • Drowsiness or sedation.
  • Extrapyramidal symptoms such as tremor, rigidity, or akathisia.
  • Dry mouth, constipation, or blurred vision.
  • Weight gain or increased appetite.
  • Orthostatic hypotension, leading to dizziness upon standing.
  • Nausea or vomiting.

Serious

  • Neuroleptic malignant syndrome, a life‑threatening reaction with fever and muscle rigidity.
  • Tardive dyskinesia, characterized by involuntary, repetitive movements.
  • Cardiac arrhythmias, including QT prolongation.
  • Severe depression or suicidal thoughts.
  • Hepatic dysfunction indicated by elevated liver enzymes.

Precautions & Warnings

When prescribing Halkid, clinicians should consider several precautionary measures to minimize risks and ensure safe use.

  • Assess for a history of cardiovascular disease, as haloperidol can prolong the QT interval.
  • Evaluate for prior movement disorders or extrapyramidal symptoms before initiating therapy.
  • Use caution in patients with hepatic or renal impairment; dose adjustments may be necessary.
  • Monitor for signs of neuroleptic malignant syndrome, especially during rapid dose escalation.
  • Avoid use in individuals with known hypersensitivity to haloperidol or other butyrophenones.
  • Consider pregnancy and lactation status; the drug’s safety profile in these populations is not well established.

Avoid Interactions

Haloperidol can interact with other medications, potentially altering its efficacy or increasing adverse effects.

Avoid

  • Other QT‑prolonging agents (e.g., certain antiarrhythmics, macrolide antibiotics) that may raise the risk of cardiac arrhythmias.
  • CNS depressants such as benzodiazepines or opioids, which can enhance sedation and respiratory depression.
  • Anticholinergic drugs that may mask extrapyramidal symptoms.

Use with caution

  • CYP3A4 inhibitors (e.g., ketoconazole, erythromycin) which can increase haloperidol plasma levels.
  • CYP3A4 inducers (e.g., carbamazepine, rifampin) that may reduce therapeutic concentrations.
  • Lithium, as combined use may increase the risk of neurotoxicity.

Frequently Asked Questions

Haloperidol is commonly prescribed for schizophrenia, acute psychotic episodes, and manic episodes associated with bipolar disorder.

It acts as a dopamine D2 receptor antagonist, reducing dopamine activity that is thought to contribute to psychotic symptoms.

Common side effects include drowsiness, extrapyramidal symptoms such as tremor or rigidity, dry mouth, constipation, and weight gain.

Haloperidol should be stopped if serious adverse reactions occur, such as neuroleptic malignant syndrome, severe cardiac arrhythmias, or intolerable extrapyramidal symptoms, after consulting a healthcare professional.

Combining haloperidol with other antipsychotics may increase the risk of side effects and should only be done under close medical supervision.

The safety of haloperidol in pregnancy has not been fully established; it should be used only if the potential benefit justifies the potential risk to the fetus.

Haloperidol can prolong the QT interval on an electrocardiogram, which may increase the risk of serious cardiac arrhythmias, especially when combined with other QT‑prolonging drugs.

Neuroleptic malignant syndrome is a rare but life‑threatening reaction characterized by high fever, muscle rigidity, autonomic instability, and altered mental status; it can occur with haloperidol use and requires immediate medical attention.

Store haloperidol at room temperature, away from excess heat, moisture, and direct sunlight, and keep it out of reach of children.

Take the missed dose as soon as you remember unless it is near the time of the next scheduled dose; do not double the dose. Consult your prescriber for specific guidance.

There are no specific dietary restrictions, but alcohol can increase sedation and should be avoided or limited.

Therapeutic effects may be observed within a few days, but full stabilization of symptoms can take several weeks of consistent treatment.

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GNH India Pharmaceuticals Limited

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Last updated:

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