Product image of Levocetirizine Dihydrochloride Bristol Laboratories (Levocetirizine Dihydrochloride) supplied by GNH India

Levocetirizine Dihydrochloride Bristol Laboratories

Active Ingredient:
Levocetirizine Dihydrochloride
Origin:
EU

Levocetirizine Dihydrochloride Bristol Laboratories (Levocetirizine Dihydrochloride)

Levocetirizine Dihydrochloride, the active ingredient in Levocetirizine Dihydrochloride Bristol Laboratories, is a second‑generation H1 receptor antagonist presented as an oral dosage form for systemic use. It is employed to relieve symptoms of allergic rhinitis and chronic idiopathic urticaria in adults and adolescents.

GNH India supplies Levocetirizine Dihydrochloride Bristol Laboratories as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides reliable logistics for global distribution, ensuring timely delivery and regulatory compliance.

Manufacturer / TM Owner

Bristol Laboratories Limited

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Indications & Clinical Uses

  • Levocetirizine Dihydrochloride is a second‑generation antihistamine that targets histamine‑mediated allergic conditions.
  • Allergic rhinitis: alleviates nasal congestion, sneezing, itching and rhinorrhea.
  • Chronic idiopathic urticaria: reduces frequency and severity of hives and associated itching.
  • Allergic conjunctivitis: relieves eye itching, redness and tearing caused by allergens.

How It Works

  • Levocetirizine Dihydrochloride selectively blocks peripheral histamine H1 receptors, preventing histamine from binding to these sites on mast cells, basophils and sensory nerves. By inhibiting this receptor activation, it diminishes the vascular permeability, edema, and sensory nerve stimulation that underlie the classic symptoms of allergic reactions, while sparing central nervous system H1 receptors, which reduces sedation significantly.

Side Effects

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

Common Side Effects

  • Drowsiness: mild sedation that may affect alertness.
  • Headache: transient cranial discomfort.
  • Dry mouth: reduced salivary flow.
  • Fatigue: generalized tiredness.

Serious or Rare Side Effects

  • Angioedema: swelling of face, lips or airway requiring urgent care.
  • Anaphylactic reaction: severe, potentially life‑threatening hypersensitivity.
  • Severe skin rash: including Stevens‑Johnson syndrome or toxic epidermal necrolysis.

Precautions & Warnings

  • When prescribing Levocetirizine Dihydrochloride, clinicians should observe the following precautions to ensure safe use.
  • Assess renal function: dose adjustment may be required in severe renal impairment.
  • Monitor hepatic status: use with caution in patients with liver disease.
  • Avoid operating machinery: drowsiness can impair psychomotor performance.
  • Observe for hypersensitivity: discontinue if signs of rash, swelling or breathing difficulty appear.
  • Pregnancy and lactation: only use if benefit outweighs potential risk to fetus or infant.
  • Store below 25°C: keep in the original pack, protect from moisture.

Avoid Interactions

Levocetirizine Dihydrochloride can interact with other medicines; awareness of major and moderate interactions helps prevent adverse outcomes.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, ritonavir): may increase levocetirizine plasma concentrations.
  • Alcohol: combined use can enhance sedation and impair cognition.

Moderate Interactions (Monitor Closely)

  • CNS depressants (e.g., benzodiazepines, opioids): additive drowsiness.
  • Other antihistamines: may increase risk of anticholinergic effects.
  • Diuretics (e.g., thiazides): may raise levocetirizine levels.

Frequently Asked Questions

Levocetirizine Dihydrochloride is indicated for the symptomatic relief of allergic rhinitis, including seasonal and perennial forms, and for the treatment of chronic idiopathic urticaria, helping to reduce hives and itching.

The drug works by selectively antagonizing peripheral histamine H1 receptors, which blocks histamine‑mediated vascular permeability, edema, and nerve stimulation, thereby alleviating the classic signs of allergic reactions without significant central sedation.

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

Safety in pregnancy and lactation has not been fully established. The drug should only be used if the potential benefit to the mother outweighs any possible risk to the fetus or infant, and this decision must be made by a qualified healthcare provider.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, and will request trade or institutional credentials before providing pricing, availability, shipping details and any necessary import documentation.

Compared with first‑generation antihistamines, Levocetirizine Dihydrochloride offers similar efficacy for allergic symptoms but with a lower incidence of sedation because it selectively targets peripheral H1 receptors while sparing central receptors.

The product should be stored below 25 °C in its original packaging, protected from moisture and direct sunlight. Maintaining these conditions helps preserve potency and ensures the medication remains stable throughout its shelf life.

Levocetirizine Dihydrochloride is taken orally, usually as a tablet, with or without food. The exact administration instructions, including timing and whether it should be taken with water, are provided by the prescribing clinician.

Serious adverse reactions, although rare, include angioedema, anaphylactic shock, and severe skin reactions such as Stevens‑Johnson syndrome. Patients should seek immediate medical attention if they experience swelling of the face or throat, difficulty breathing, or a widespread rash.

Individuals with known hypersensitivity to levocetirizine or any component of the formulation should avoid the drug. Caution is also advised for patients with severe renal impairment, as dose adjustment may be required, and for those taking interacting medications.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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