Product image of Oxomémazine Sans Sucre Édulcorée À L’acésulfame Potassique Benta (Oxomemazine) supplied by GNH India

Oxomémazine Sans Sucre Édulcorée À L’acésulfame Potassique Benta

Active Ingredient:
Oxomemazine
Origin:
EU

Oxomémazine Sans Sucre Édulcorée À L’acésulfame Potassique Benta (Oxomemazine)

Oxomemazine, the active ingredient in Oxomémazine Sans Sucre Édulcorée À L’acésulfame Potassique Benta, is a antihistamine presented as a sugar‑free oral formulation for oral use. It is employed to relieve allergic symptoms and to provide sedation in pediatric and adult patients when indicated.

GNH India supplies Oxomémazine Sans Sucre Édulcorée À L’acésulfame Potassique Benta as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and pharmacies worldwide.

Manufacturer / TM Owner

Benta Sas

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Indications & Clinical Uses

Oxomemazine is a first‑generation H1‑receptor antagonist that acts on allergic and central nervous system pathways. It is commonly used for:

  • Allergic rhinitis: reduces nasal congestion, itching and sneezing.
  • Acute urticaria: alleviates hives and associated itching.
  • Pre‑operative sedation: provides mild sedation and anxiolysis before minor procedures.
  • Cough associated with upper respiratory infections: suppresses the cough reflex.
  • Motion sickness prophylaxis: helps prevent nausea and vomiting related to travel.

How It Works

  • Oxomemazine blocks histamine H1 receptors in peripheral tissues, reducing the vascular and sensory effects of histamine release. It also penetrates the central nervous system, where antagonism of central H1 receptors produces sedative and anti‑emetic effects, contributing to its utility in cough suppression and pre‑operative calming.

Side Effects

Oxomemazine may cause a range of adverse reactions, most of which are dose‑dependent and reversible.

Common Side Effects

  • Drowsiness: feeling unusually sleepy or fatigued.
  • Dry mouth: reduced salivation leading to a sticky sensation.
  • Dizziness: light‑headed feeling, especially when standing quickly.
  • Blurred vision: temporary difficulty focusing.
  • Constipation: reduced bowel movements.
  • Nausea: mild stomach upset.

Serious or Rare Side Effects

  • Cardiac arrhythmias: irregular heart rhythm, particularly in patients with pre‑existing heart disease.
  • Extrapyramidal symptoms: involuntary muscle movements or tremor.
  • Severe allergic reaction: rash, swelling, or difficulty breathing.
  • Hepatotoxicity: signs of liver injury such as jaundice.
  • Hematologic abnormalities: unexplained bruising or bleeding.
  • Seizures: rare occurrence of convulsive episodes.

Precautions & Warnings

When prescribing oxomemazine, clinicians should consider several safety aspects:

  • Pregnancy: avoid use unless clearly needed, as safety data are limited.
  • Breastfeeding: monitor infant for sedation; consider alternative therapy.
  • Elderly patients: start with lower doses due to increased sensitivity to sedation.
  • Concomitant CNS depressants: risk of enhanced drowsiness and respiratory depression.
  • Driving and machinery: advise patients not to operate vehicles or heavy equipment until they know how the drug affects them.
  • Store at below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Oxomemazine can interact with several drug classes, requiring attention to dosing and monitoring.

Major Interactions (Avoid)

  • Monoamine oxidase inhibitors (MAOIs): risk of severe hypotension and sedation.
  • Other antihistamines: additive sedative effects and anticholinergic burden.
  • CNS depressants (e.g., benzodiazepines, opioids): heightened risk of respiratory depression.

Moderate Interactions (Monitor Closely)

  • Anticholinergic drugs (e.g., atropine, ipratropium): may increase dry‑mouth and urinary retention.
  • CYP450 inhibitors (e.g., erythromycin, fluconazole): can raise oxomemazine plasma levels.
  • Alcohol: enhances drowsiness and impairment of coordination.

Frequently Asked Questions

Oxomémazine Sans Sucre Édulcorée is an oral antihistamine indicated for allergic rhinitis, acute urticaria, cough associated with upper‑respiratory infections, pre‑operative sedation and motion‑sickness prophylaxis. It helps relieve itching, sneezing, nasal congestion and provides mild calming effects when needed.

Oxomemazine blocks peripheral H1 histamine receptors, limiting the vascular leakage and sensory irritation caused by histamine. It also crosses the blood‑brain barrier, antagonising central H1 receptors, which produces sedation and suppresses the cough reflex, explaining its use in pre‑operative calming and cough control.

The appropriate dose of oxomemazine is determined by the prescribing clinician based on the patient’s age, weight, indication and clinical response. Healthcare professionals should follow local prescribing guidelines and adjust the regimen as needed for safety and efficacy.

Oxomemazine should be used in pregnancy only if the potential benefit justifies any potential risk to the fetus, as safety data are limited. During breastfeeding, the drug may pass into milk and cause infant sedation; therefore, caution is advised and alternative treatments should be considered when possible.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Oxomemazine is a first‑generation H1 antagonist, offering both peripheral antihistamine effects and central sedation, unlike many second‑generation agents that lack sedative properties. This makes it useful when a calming effect is desired, but it also carries a higher risk of drowsiness and anticholinergic side effects.

Store Oxomémazine Sans Sucre Édulcorée at temperatures below 25 °C, in its original packaging, protected from moisture and direct sunlight. Maintaining these conditions helps preserve potency and prevents degradation of the sugar‑free formulation.

Oxomemazine is supplied as an oral tablet that should be swallowed whole with water. It is taken by mouth according to the prescriber’s instructions, typically with or without food, depending on the specific clinical scenario.

Serious adverse reactions can include cardiac arrhythmias, extrapyramidal symptoms, severe allergic responses, hepatotoxicity, hematologic abnormalities and, rarely, seizures. Patients should be monitored for any signs of these events, especially if they have pre‑existing cardiac or liver conditions.

Oxomemazine is contraindicated in individuals with known hypersensitivity to the drug or other first‑generation antihistamines, as well as in patients taking mono‑amine oxidase inhibitors. Caution is also advised for those with severe hepatic impairment, uncontrolled glaucoma, or a history of cardiac arrhythmias.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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