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

Levocetirizin Krka

Active Ingredient:
Levocetirizine Dihydrochloride
Origin:
EU

Levocetirizin Krka (Levocetirizine Dihydrochloride)

Levocetirizine Dihydrochloride, the active ingredient in Levocetirizin Krka, is an antihistamine presented as an oral tablet for oral use. It selectively blocks peripheral H1 receptors, providing relief from symptoms of allergic rhinitis such as sneezing, nasal congestion and itchy eyes, as well as reducing hives and itching associated with chronic urticaria in both adult and pediatric patients.

GNH India supplies Levocetirizin Krka as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring consistent quality and regulatory compliance across global markets.

Manufacturer / TM Owner

Krka, D.D., Novo Mesto

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Indications & Clinical Uses

Levocetirizin is an antihistamine that acts on the H1‑receptor pathway to alleviate allergic conditions.

  • Allergic rhinitis: reduces nasal congestion, sneezing, itching and watery eyes associated with seasonal or perennial allergens.
  • Chronic idiopathic urticaria: diminishes the frequency and severity of hives and associated itching.
  • Allergic conjunctivitis: alleviates eye redness, itching and tearing caused by allergen exposure.

How It Works

  • Levocetirizine Dihydrochloride is a selective peripheral H1‑receptor antagonist. By binding with high affinity to histamine H1 receptors on mast cells, basophils and vascular endothelium, it prevents histamine‑induced vasodilation, increased vascular permeability and sensory nerve stimulation. This blockade reduces the classic symptoms of allergic reactions without crossing the blood‑brain barrier in significant amounts, thereby limiting central nervous system effects.

Side Effects

Levocetirizin may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Drowsiness: mild to moderate sleepiness, especially after the first dose.
  • Fatigue: general feeling of tiredness.
  • Dry mouth: reduced salivation leading to a dry oral cavity.
  • Headache: mild to moderate head pain.
  • Nausea: occasional stomach upset.
  • Taste disturbance: altered perception of flavors.

Serious or Rare Side Effects

  • Angioedema: swelling of face, lips, tongue or throat requiring immediate medical attention.
  • Anaphylactic reaction: severe, rapid‑onset allergic response that can be life‑threatening.
  • Blood dyscrasias: rare cases of neutropenia or thrombocytopenia.

Precautions & Warnings

Before prescribing Levocetirin, clinicians should consider several precautionary measures to ensure safe use.

  • Renal function assessment: adjust dose in patients with severe renal impairment.
  • Concomitant CNS depressants: avoid or monitor use with alcohol, benzodiazepines or opioids due to additive sedation.
  • Driving and machinery: caution patients who experience drowsiness before operating vehicles or heavy equipment.
  • Pregnancy and lactation: use only if potential benefit justifies potential risk, as safety data are limited.
  • Elderly patients: start at the lowest effective dose and monitor for increased sensitivity.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging and protect from moisture.

Avoid Interactions

Levocetirizin can interact with other medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Ketoconazole or other strong CYP3A4 inhibitors: may increase levocetirizin plasma levels and risk of sedation.
  • Other H1‑antihistamines: concurrent use can enhance anticholinergic effects and excessive sedation.
  • Monoamine oxidase inhibitors (MAOIs): may potentiate central nervous system depression.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers such as rifampicin: may reduce levocetirizin exposure and effectiveness.
  • CNS depressants (e.g., alcohol, sedative hypnotics): may increase drowsiness.
  • Theophylline: may experience altered theophylline metabolism.

Frequently Asked Questions

Levocetirizin Krka contains levocetirizine dihydrochloride, an antihistamine indicated for the symptomatic relief of allergic rhinitis and chronic idiopathic urticaria. It helps reduce nasal congestion, sneezing, itching, watery eyes, and the frequency and severity of hives in patients of appropriate age as determined by a healthcare professional.

Levocetirizine dihydrochloride works by selectively binding to peripheral histamine H1 receptors. This antagonism blocks the action of histamine released during allergic reactions, preventing vasodilation, increased vascular permeability, and sensory nerve stimulation, thereby alleviating typical allergy symptoms without significant central nervous system penetration.

The dosage of Levocetirizin Krka is individualized by the prescribing clinician based on the patient’s age, renal function, and severity of symptoms. In many regions the standard adult dose is 5 mg once daily, but the exact regimen should always follow the prescriber’s written instructions.

Safety data for levocetirizine in pregnancy and lactation are limited. It should only be used if the potential therapeutic benefit justifies any possible risk to the fetus or infant. Women who are pregnant, planning pregnancy, or breastfeeding should discuss the risks and alternatives with their healthcare provider.

To place an order, submit an enquiry on the Levocetirin Krka 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 (including any cold‑chain requirements) and necessary import documentation.

Levocetirin (levocetirizine) is the active enantiomer of cetirizine, offering a similar efficacy profile with a slightly lower incidence of sedation for many patients. Compared with first‑generation antihistamines, it provides better selectivity for peripheral H1 receptors and fewer anticholinergic side effects, making it a preferred option for chronic allergy management.

Store Levocetirin Krka at ambient temperature, preferably below 25 °C. Keep the tablets in the original blister pack or container, protect them from moisture and direct sunlight, and ensure they are out of reach of children. Do not store in a refrigerator or freezer.

Levocetirin is taken orally, usually as a whole tablet with or without food. Patients should swallow the tablet with a glass of water and follow the dosing schedule prescribed by their clinician. The medication should not be crushed, chewed, or dissolved unless specifically instructed.

Serious adverse reactions, although rare, include angioedema, anaphylaxis, and severe blood dyscrasias such as neutropenia or thrombocytopenia. Patients should seek immediate medical attention if they experience swelling of the face, lips, tongue, or throat, difficulty breathing, or unexplained bruising or bleeding.

Levocetirin is contraindicated in individuals with known hypersensitivity to levocetirizine, cetirizine, or any other component of the formulation. Caution is also advised for patients with severe renal impairment, as dose adjustment may be required, and for those taking interacting medications listed under major interactions.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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