Product image of Lentrica (Desloratadine) supplied by GNH India

Lentrica

Active Ingredient:
Desloratadine
Origin:
EU

Lentrica (Desloratadine)

Desloratadine, the active ingredient in Lentrica, is a second‑generation H1 antagonist presented as an oral tablet for oral use. It treats allergic rhinitis and chronic idiopathic urticaria by reducing histamine‑mediated symptoms in adults and children.

GNH India supplies Lentrica as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Lek Pharmaceuticals D.D. Ljubljana

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Indications & Clinical Uses

  • Desloratadine is a second‑generation antihistamine that reduces histamine‑mediated symptoms in allergic conditions.
  • Allergic rhinitis: relief of nasal congestion, sneezing, itching and watery discharge.
  • Chronic idiopathic urticaria: reduction of hives and associated itching.
  • Allergic conjunctivitis: alleviation of eye itching, redness and tearing.

How It Works

  • Desloratadine selectively blocks peripheral H1 receptors, preventing histamine from binding and activating the cascade that leads to vasodilation, increased vascular permeability, and sensory nerve stimulation. By inhibiting this pathway, it diminishes the classic signs of allergic inflammation without readily crossing the blood‑brain barrier, which limits central nervous system effects.

Side Effects

Desloratadine is generally well tolerated, but adverse reactions can occur.

Common Side Effects

  • Headache: mild to moderate intensity.
  • Dry mouth: transient sensation of oral dryness.
  • Fatigue or mild somnolence: occasional tiredness.
  • Nausea: occasional upset stomach.
  • Dizziness: brief light‑headed feeling.

Serious or Rare Side Effects

  • Angioedema: swelling of face, lips or throat requiring urgent care.
  • Severe skin reactions: such as Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Anaphylaxis: rapid onset of systemic allergic response.
  • Cardiac arrhythmia: rare reports of irregular heartbeat.
  • Hepatotoxicity: very rare liver enzyme elevations.

Precautions & Warnings

  • Before using Lentrica, consider the following safety points.
  • Hepatic impairment: dose may need adjustment in patients with severe liver disease.
  • Known hypersensitivity: avoid if the patient has demonstrated allergy to desloratadine or related antihistamines.
  • Pregnancy: consult a healthcare professional; benefits should outweigh potential risks.
  • Breastfeeding: discuss with a physician as drug may pass into milk.
  • Sedation potential: exercise caution when driving or operating machinery until individual response is known.
  • Store at room temperature: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Desloratadine may interact with other medicines; monitor accordingly.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): may increase desloratadine plasma levels.
  • Concurrent use with other H1 antihistamines: can enhance sedative effects.

Moderate Interactions (Monitor Closely)

  • Alcohol or CNS depressants: may increase drowsiness.
  • CYP3A4 substrates (e.g., erythromycin, ritonavir): monitor for altered efficacy.
  • Anticholinergic agents: may exacerbate dry mouth.
  • Herbal supplements such as St. John’s wort: could reduce drug exposure.

Frequently Asked Questions

Lentrica contains desloratadine, a second‑generation antihistamine indicated for relief of symptoms associated with allergic rhinitis and chronic idiopathic urticaria. It helps reduce nasal congestion, sneezing, itching, and hives by blocking histamine receptors in the peripheral tissues.

Desloratadine selectively antagonizes peripheral H1 receptors, preventing histamine from binding and triggering the cascade that leads to vasodilation, increased vascular permeability, and sensory nerve activation. This blockade reduces the classic signs of allergic inflammation without significant central nervous system penetration.

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

Safety data for desloratadine in 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 starting Lentrica.

To request Lentrica, 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.

Compared with first‑generation antihistamines, desloratadine offers similar efficacy for allergic symptoms but with a lower likelihood of sedation because it does not readily cross the blood‑brain barrier. It is also more selective than some second‑generation agents, providing a favorable safety profile for long‑term use.

Lentrica should be stored at room temperature, below 25 °C, in its original packaging. Keep the product away from moisture, direct sunlight and excessive heat to maintain its stability and potency throughout its shelf life.

Lentrica 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 chewed or crushed unless specifically instructed.

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

Lentrica is contraindicated in individuals with known hypersensitivity to desloratadine or any component of the formulation. Caution is also advised for patients with severe hepatic impairment, and it should be avoided in those taking medications that may cause dangerous drug‑drug interactions without medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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