Product image of Levocetirizina Sandoz (Levocetirizine Dihydrochloride) supplied by GNH India

Levocetirizina Sandoz

Active Ingredient:
Levocetirizine Dihydrochloride
Origin:
EU

Levocetirizina Sandoz (Levocetirizine Dihydrochloride)

Levocetirizine, the active ingredient in Levocetirizina Sandoz, is a second‑generation antihistamine presented as an oral tablet for systemic use, providing relief of allergic symptoms such as sneezing, itching and rhinorrhea in patients with allergic rhinitis or chronic idiopathic urticaria.

GNH India supplies Levocetirizina Sandoz as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, with established logistics networks and regulatory expertise to ensure reliable, quality‑assured delivery across multiple regions, including Europe, Asia and the Americas.

Manufacturer / TM Owner

Sandoz Farmacéutica, S.A.

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Indications & Clinical Uses

Levocetirizine is a second‑generation antihistamine that reduces histamine‑mediated allergic responses.

  • Allergic rhinitis: alleviates sneezing, nasal itching, congestion and rhinorrhea.
  • Chronic idiopathic urticaria: decreases frequency and severity of hives and associated itching.
  • Seasonal allergic rhinitis: controls symptoms triggered by pollen exposure.
  • Perennial allergic rhinitis: provides year‑round symptom relief.

How It Works

  • Levocetirizine acts as a selective antagonist of peripheral histamine H1 receptors. By binding to these receptors on mast cells, basophils and sensory nerves, it blocks the action of endogenous histamine released during allergic reactions, thereby preventing the cascade that leads to vasodilation, increased vascular permeability, itching and sneezing.

Side Effects

Levocetirizine is generally well tolerated, but some patients may experience adverse reactions.

Common Side Effects

  • Headache: mild to moderate pain often resolving without intervention.
  • Dry mouth: sensation of oral dryness that may improve with hydration.
  • Drowsiness or fatigue: occasional mild sedation, especially at the start of therapy.
  • Nausea: transient stomach upset that usually subsides.
  • Taste alteration: temporary changes in flavor perception.

Serious or Rare Side Effects

  • Angioedema: swelling of face, lips or tongue requiring immediate medical attention.
  • Anaphylactic reaction: severe, potentially life‑threatening hypersensitivity.
  • Severe skin reactions: such as Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Cardiac arrhythmia: rare reports of rhythm disturbances.
  • Hepatic dysfunction: uncommon elevation of liver enzymes.

Precautions & Warnings

Before initiating therapy, consider the following safety measures.

  • Assess renal function: dose adjustment may be needed in severe impairment.
  • Evaluate hepatic status: monitor liver enzymes if pre‑existing disease exists.
  • Avoid operating machinery: drowsiness can impair alertness.
  • Use caution in pregnancy: discuss risks with a healthcare professional.
  • Limit alcohol consumption: may potentiate sedation.
  • Store at ambient temperature: keep in the original pack, protect from moisture.

Avoid Interactions

Levocetirizine may interact with several medicines; monitoring is advised.

Major Interactions (Avoid)

  • Ketoconazole: can increase levocetirizine plasma concentrations.
  • Erythromycin: may raise systemic exposure.
  • Ritonavir: potential for elevated drug levels.

Moderate Interactions (Monitor Closely)

  • Alcohol: may enhance sedative effects.
  • Other antihistamines: additive drowsiness risk.
  • Theophylline: may increase its clearance, reducing efficacy.

Frequently Asked Questions

Levocetirizina Sandoz contains levocetirizine, which is indicated for the symptomatic treatment of allergic rhinitis—including seasonal and perennial forms—and for chronic idiopathic urticaria, helping to reduce sneezing, itching, nasal discharge and hives.

Levocetirizine selectively blocks peripheral H1 histamine receptors on mast cells, basophils and sensory nerves. By preventing histamine from binding, it stops the cascade that causes vasodilation, increased capillary permeability, itching and sneezing, thereby reducing allergic manifestations.

The appropriate dose of Levocetirizina Sandoz is determined by the prescribing healthcare professional based on the patient’s age, severity of symptoms and renal function. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety data in pregnancy and lactation are limited. The medication should only be used if the potential benefit justifies any possible risk to the fetus or infant, and this decision must be made by a qualified healthcare provider after a thorough assessment.

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.

Levocetirizina Sandoz is a second‑generation antihistamine, offering effective symptom control with a lower incidence of sedation compared with first‑generation agents. Its rapid onset and once‑daily dosing make it convenient, while its selectivity for H1 receptors reduces central nervous system side effects.

Store the tablets at ambient temperature, preferably below 25 °C, in the original packaging to protect them from moisture and light. Keep the product out of reach of children and do not use it after the expiry date printed on the label.

Levocetirizina Sandoz is taken orally, usually once daily with or without food, as directed by the prescriber. Swallow the tablet whole with a glass of water; do not crush or chew unless specifically instructed.

Serious adverse reactions, although rare, include angioedema, anaphylaxis, severe skin reactions such as Stevens‑Johnson syndrome, and cardiac arrhythmias. Patients should seek immediate medical attention if they experience swelling of the face or throat, rash, or any signs of an allergic emergency.

Individuals with known hypersensitivity to levocetirizine or any component of the formulation should not use the product. Caution is also advised for patients with severe renal impairment, and it should be avoided in pregnancy or lactation unless clearly indicated by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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