Product image of Levocetirizin Stada (Levocetirizine Dihydrochloride) supplied by GNH India

Levocetirizin Stada

Active Ingredient:
Levocetirizine Dihydrochloride
Origin:
EU

Levocetirizin Stada (Levocetirizine Dihydrochloride)

Levocetirizine, the active ingredient in Levocetirizin Stada, is a second‑generation H1 antihistamine presented as an oral dosage form for oral use. It is indicated for the relief of symptoms associated with allergic rhinitis and chronic idiopathic urticaria in adults and children.
GNH India supplies Levocetirizin Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Stada Arzneimittel Ag

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Indications & Clinical Uses

  • Levocetirizin Stada is a second‑generation H1 antihistamine that acts on allergic pathways to alleviate symptoms.
  • Allergic rhinitis: reduces nasal congestion, sneezing, itching and rhinorrhea caused by seasonal or perennial allergens.
  • Chronic idiopathic urticaria: diminishes wheal formation and itching in patients with persistent hives.

How It Works

  • Levocetirizine is a selective antagonist of peripheral H1 histamine receptors. By binding to these receptors, it blocks the action of histamine released during allergic reactions, thereby preventing the cascade that leads to vasodilation, increased vascular permeability, and sensory nerve stimulation that cause typical allergy symptoms.

Side Effects

Levocetirizin Stada may cause adverse reactions, most of which are mild and reversible.

Common Side Effects

  • Headache: mild to moderate pain often reported during early treatment.
  • Somnolence: transient drowsiness, especially after the first doses.
  • Dry mouth: reduced salivation leading to a feeling of oral dryness.
  • Fatigue: general tiredness without loss of consciousness.
  • Dizziness: light‑headed sensation that usually resolves with continued use.

Serious or Rare Side Effects

  • Anaphylaxis: acute, life‑threatening allergic reaction requiring immediate medical attention.
  • Angioedema: swelling of the face, lips, tongue or throat that may compromise airway.
  • Severe skin reactions: such as Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Cardiac arrhythmia: rare reports of irregular heart rhythm.
  • Hepatic injury: uncommon elevation of liver enzymes.

Precautions & Warnings

  • Before initiating therapy with Levocetirizin Stada, consider the following precautions.
  • Pregnancy: consult a healthcare professional; safety data are limited.
  • Renal impairment: dose adjustment may be necessary in patients with reduced kidney function.
  • Elderly: monitor for increased sedation or confusion.
  • Concomitant CNS depressants: may enhance drowsiness and impair coordination.
  • Store at ambient temperature: keep below 25 °C, protect from moisture and light in the original packaging.

Avoid Interactions

Levocetirizin Stada can interact with other medicines; awareness of the interaction level helps manage risk.

Major Interactions (Avoid)

  • Potent CYP3A4 inhibitors: may raise levocetirizine plasma concentrations.
  • Alcohol: additive central nervous system depression leading to excessive sedation.

Moderate Interactions (Monitor Closely)

  • Other sedating antihistamines: may increase drowsiness.
  • Ritonavir: can elevate levocetirizine exposure.
  • Theophylline: may result in higher theophylline levels.
  • Anticholinergic agents: could exacerbate dry‑mouth effects.

Frequently Asked Questions

Levocetirizin Stada contains levocetirizine, a second‑generation H1 antihistamine indicated for the symptomatic relief of allergic rhinitis and for the management of chronic idiopathic urticaria, helping to reduce nasal symptoms and itching associated with hives.

Levocetirizine selectively blocks peripheral H1 histamine receptors, preventing histamine from binding and triggering the cascade that leads to vasodilation, increased vascular permeability, and sensory nerve activation, thereby alleviating typical allergy symptoms.

The appropriate dose of Levocetirizin Stada is determined by the prescribing healthcare professional based on the patient’s age, weight, renal function and clinical response. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety data for levocetirizine during pregnancy and lactation are limited. Women who are pregnant, planning to become pregnant, or breastfeeding should discuss potential risks and benefits with their healthcare provider before using Levocetirizin Stada.

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.

Levocetirizin Stada is a second‑generation antihistamine, offering effective allergy relief with a lower incidence of sedation compared with first‑generation agents. It provides a rapid onset of action and is often preferred when daytime drowsiness is a concern.

The product should be stored at ambient temperature, preferably below 25 °C, in its original packaging to protect it from moisture and light. No refrigeration is required for this oral formulation.

Levocetirizin Stada is taken orally, usually with or without food, as directed by the prescriber. The tablet should be swallowed whole with a glass of water and not crushed or chewed unless otherwise instructed.

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

Levocetirizin Stada should be avoided in individuals with known hypersensitivity to levocetirizine or any of the excipients. Caution is also advised for patients with severe renal impairment, and it should be used only under medical supervision in pregnant or breastfeeding women.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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