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

Oxomemazine Sans Sucre, Édulcorée À L’acésulfame Potassique Unither

Active Ingredient:
Oxomemazine
Origin:
EU

Oxomemazine Sans Sucre, Édulcorée À L’acésulfame Potassique Unither (Oxomemazine)

Oxomemazine, the active ingredient in Oxomemazine Sans Sucre, Édulcorée À L’acésulfame Potassique Unither, is a antihistamine presented as a sugar‑free oral formulation for pediatric and adult use. It is employed to alleviate symptoms of allergic reactions and related respiratory discomfort in patients of various ages.

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

Manufacturer / TM Owner

Unither Pharmaceuticals

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Indications & Clinical Uses

Oxomemazine is a first‑generation antihistamine that acts on histamine‑mediated pathways to reduce allergic symptoms.

  • Allergic rhinitis: helps relieve nasal congestion, itching and sneezing.
  • Acute urticaria: reduces the formation of hives and associated itching.
  • Cough associated with upper respiratory tract infections: diminishes cough frequency and severity.

How It Works

  • Oxomemazine blocks H1 histamine receptors in peripheral tissues and the central nervous system, preventing histamine‑induced vasodilation, increased vascular permeability, and sensory nerve activation. This antagonism reduces the classic signs of allergy such as itching, swelling, and bronchoconstriction, and also exerts a mild sedative effect through central H1 blockade.

Side Effects

Oxomemazine may cause a range of adverse reactions, most of which are mild and reversible.

Common Side Effects

  • Drowsiness: a feeling of sleepiness or reduced alertness.
  • Dry mouth: reduced salivation leading to a dry oral cavity.
  • Dizziness: light‑headed sensation, especially when standing quickly.
  • Gastrointestinal discomfort: nausea or mild stomach upset.
  • Blurred vision: temporary visual disturbances.

Serious or Rare Side Effects

  • Cardiac arrhythmias: irregular heart rhythm requiring medical attention.
  • Severe allergic reactions: rash, swelling, or difficulty breathing.
  • Extrapyramidal symptoms: involuntary muscle movements or tremor.
  • Hepatotoxicity: signs of liver injury such as jaundice.

Precautions & Warnings

Before prescribing Oxomemazine, clinicians should consider several safety aspects.

  • Pregnancy: avoid use unless the benefit outweighs the risk.
  • Breastfeeding: monitor infant for sedation; consider alternatives.
  • Elderly patients: start with lower doses due to increased sensitivity to sedation.
  • Concomitant CNS depressants: may enhance drowsiness and impair coordination.
  • Driving or operating machinery: advise patients to avoid 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 other medications, altering efficacy or safety.

Major Interactions (Avoid)

  • Monoamine oxidase inhibitors (MAOIs): risk of hypertensive crisis.
  • Other antihistamines: additive sedation and anticholinergic effects.
  • CNS depressants (e.g., benzodiazepines, opioids): heightened central nervous system depression.

Moderate Interactions (Monitor Closely)

  • Alcohol: may increase drowsiness.
  • Anticholinergic drugs: potential for excessive dry mouth and urinary retention.
  • Cardiac glycosides: possible alteration of heart rhythm.

Frequently Asked Questions

Oxomemazine Sans Sucre is a sugar‑free antihistamine indicated for relief of allergic rhinitis, acute urticaria and cough associated with upper‑respiratory infections. It helps reduce itching, sneezing, nasal congestion and cough frequency in patients of various ages.

Oxomemazine blocks H1 histamine receptors in peripheral tissues and the central nervous system. By preventing histamine binding, it limits vasodilation, vascular permeability and sensory nerve activation, which alleviates typical allergy symptoms and provides a mild sedative effect.

The dosage of oxomemazine is individualized by the prescribing clinician based on the patient’s age, weight, condition severity and response. Healthcare professionals determine the appropriate strength and frequency according to local prescribing guidelines.

Oxomemazine should only be used in pregnancy when the potential benefit justifies the risk to the fetus. During breastfeeding, the drug may pass into milk and cause sedation in the infant; therefore, caution is advised and alternatives 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 strong antihistaminic activity and a mild sedative effect. Compared with second‑generation antihistamines, it may cause more drowsiness but can be useful when a sedative component is desired, such as for nighttime cough relief.

Store the tablets below 25 °C in their original container, protected from moisture and direct sunlight. Keep the packaging tightly closed to maintain product stability throughout its shelf life.

The product is taken orally, usually with a glass of water. Patients should follow the prescribing clinician’s instructions regarding timing, whether with or without food, and any necessary dose adjustments.

Serious adverse reactions, though rare, include cardiac arrhythmias, severe allergic responses such as anaphylaxis, extrapyramidal symptoms and liver injury. Immediate medical attention is required if any of these events occur.

Oxomemazine is contraindicated in patients with known hypersensitivity to the drug or other first‑generation antihistamines, and should be avoided in individuals taking mono‑amine oxidase inhibitors. Caution is also advised for patients with severe hepatic impairment or uncontrolled cardiac conditions.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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