Product image of Haloperidol Syri (Haloperidol) supplied by GNH India

Haloperidol Syri

Active Ingredient:
Haloperidol
Origin:
EU

Haloperidol Syri (Haloperidol)

Haloperidol Syri is an oral formulation of the generic drug haloperidol, a butyrophenone antipsychotic. While the specific strength is not disclosed, the product is marketed in the European Union and is available by prescription only. Haloperidol works by blocking dopamine D2 receptors, which helps manage symptoms of certain psychiatric conditions. It is classified under ATC code N05AD01 and is typically used under the supervision of a qualified healthcare professional.

Manufacturer / TM Owner

Syri Limited T/A Thame Laboratories

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Indications & Clinical Uses

Haloperidol Syri is prescribed for several psychiatric indications where dopamine blockade is therapeutic, and it may be used as part of a broader treatment plan.

  • Management of schizophrenia, including acute exacerbations.
  • Treatment of acute psychotic episodes unrelated to schizophrenia.
  • Control of manic episodes in bipolar disorder.
  • Reduction of severe agitation or aggression in hospitalized patients.
  • Adjunctive therapy for Tourette syndrome when other options are insufficient.
  • Prevention of relapse in patients stabilized on haloperidol therapy.
  • Use in combination with other antipsychotics when monotherapy is inadequate.

Side Effects

Haloperidol Syri can produce a range of adverse effects, which are generally categorized by frequency and severity; patients should be monitored regularly for both common and potentially serious reactions.

Common

  • Extrapyramidal symptoms such as tremor, rigidity, and akathisia.
  • Drowsiness or sedation.
  • Dry mouth and constipation.
  • Weight gain or increased appetite.
  • Blurred vision or ocular disturbances.
  • Nausea or vomiting.
  • Orthostatic hypotension.
  • Insomnia or sleep disturbances.
  • Sexual dysfunction, such as decreased libido.

Serious

  • Neuroleptic malignant syndrome, a life‑threatening reaction.
  • Tardive dyskinesia, characterized by involuntary movements.
  • Significant cardiac arrhythmias, including QT prolongation.
  • Severe depression or suicidal thoughts.
  • Hepatic dysfunction with elevated enzymes.
  • Seizures in predisposed individuals.
  • Elevated prolactin levels leading to galactorrhea.

Precautions & Warnings

When prescribing Haloperidol Syri, clinicians consider several precautionary factors to minimize risk and ensure appropriate use.

  • Assess patient history for cardiovascular disease, especially arrhythmias or prolonged QT interval.
  • Evaluate for movement disorders or prior extrapyramidal reactions before initiating therapy.
  • Use caution in patients with hepatic or renal impairment; dose adjustments may be required.
  • Monitor for signs of neuroleptic malignant syndrome during the first weeks of treatment.
  • Consider pregnancy and lactation status; the safety profile in these populations is not well established.
  • Review concomitant medications that may increase the risk of sedation or cardiac effects.

Avoid Interactions

Haloperidol Syri may interact with other medicines, altering its effectiveness or increasing adverse effects; awareness of key interactions guides safe prescribing.

Avoid

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin) that can raise haloperidol plasma levels.
  • Other antipsychotics or dopamine antagonists that may exacerbate extrapyramidal symptoms.
  • Medications known to prolong the QT interval, such as certain antiarrhythmics or fluoroquinolones.

Use with caution

  • CNS depressants (e.g., benzodiazepines, opioids) that can increase sedation.
  • Anticholinergic agents, which may mask early signs of extrapyramidal side effects.
  • CYP2D6 substrates (e.g., metoprolol, codeine) where haloperidol may affect their metabolism.

Frequently Asked Questions

Haloperidol Syri is typically used to treat schizophrenia, acute psychotic episodes, manic phases of bipolar disorder, and severe agitation that requires rapid control.

The medication blocks dopamine D2 receptors in the central nervous system, reducing dopamine activity that is associated with psychotic symptoms and mood instability.

Common adverse effects include extrapyramidal symptoms such as tremor or rigidity, drowsiness, dry mouth, constipation, weight changes, blurred vision, nausea, and orthostatic hypotension.

Serious reactions include neuroleptic malignant syndrome, tardive dyskinesia, significant cardiac arrhythmias (especially QT prolongation), severe depression or suicidal thoughts, hepatic dysfunction, seizures, and elevated prolactin causing galactorrhea.

The safety of haloperidol during pregnancy has not been definitively established; clinicians weigh potential benefits against unknown risks and consider alternative therapies when possible.

Store the medication at room temperature, away from excess heat, moisture, and direct sunlight. Keep it out of reach of children and pets.

No specific dietary restrictions are required, but patients should avoid excessive alcohol consumption, which can increase sedation and other central nervous system effects.

Inform your healthcare provider about any heart conditions, liver or kidney disease, history of movement disorders, current medications, pregnancy or breastfeeding status, and any previous adverse reactions to antipsychotics.

Combining haloperidol with other dopamine antagonists can heighten the risk of extrapyramidal symptoms and other side effects, so such combinations are generally avoided unless specifically directed by a specialist.

Alcohol can potentiate the sedative effects of haloperidol and may increase the likelihood of dizziness or impaired judgment; it is advisable to limit or avoid alcohol while on therapy.

Regular monitoring may include assessment of movement disorders, cardiac ECG for QT interval, liver function tests, blood glucose, and observation for signs of neuroleptic malignant syndrome.

Clinical improvement in psychotic symptoms may be observed within a few days, but full therapeutic response can take several weeks, depending on the individual and the condition being treated.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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