Product image of Kestine 20 (Ebastine) supplied by GNH India

Kestine 20

Active Ingredient:
Ebastine
Origin:
EU

Kestine 20 (Ebastine)

Ebastine, the active ingredient in Kestine 20, is a second‑generation H1‑receptor antagonist presented as a 20 mg tablet for oral use. It is indicated for the treatment of allergic conditions such as allergic rhinitis and chronic idiopathic urticaria, providing relief from itching, swelling and other histamine‑mediated symptoms in adults and adolescents.

GNH India supplies Kestine 20 as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and regulatory requirements to ensure product consistency across global markets.

Manufacturer / TM Owner

Almirall, S.A.

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Indications & Clinical Uses

Ebastine acts on histamine‑mediated allergic pathways, providing relief in several common allergic conditions.

  • Allergic rhinitis: reduces nasal congestion, sneezing and itching associated with seasonal or perennial triggers.
  • Chronic idiopathic urticaria: alleviates hives and itching by stabilizing mast cell response.
  • Allergic skin symptoms: diminishes itching and swelling caused by histamine release in various dermatologic allergic reactions.

How It Works

  • Ebastine selectively blocks peripheral H1 histamine receptors without readily crossing the blood‑brain barrier. By antagonizing H1 receptors on mast cells, endothelial cells and sensory nerves, it prevents histamine‑induced vasodilation, increased vascular permeability, and nerve stimulation, thereby reducing symptoms such as itching, swelling, and nasal congestion associated with allergic reactions. The drug exhibits high affinity for the H1 receptor and a long plasma half‑life, allowing once‑daily dosing while minimizing central nervous system effects.

Side Effects

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

Common Side Effects

  • Headache: mild to moderate intensity.
  • Dry mouth: transient sensation of oral dryness.
  • Drowsiness: occasional mild sedation, less frequent than with first‑generation antihistamines.
  • Nausea: mild gastrointestinal upset.
  • Fatigue: feeling of reduced energy.
  • Dizziness: occasional light‑headedness.

Serious or Rare Side Effects

  • Angioedema: swelling of face, lips or throat requiring immediate medical attention.
  • Severe skin reactions: such as Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Cardiac arrhythmias: rare QT interval prolongation leading to rhythm disturbances.
  • Anaphylaxis: acute, life‑threatening allergic reaction.
  • Hepatic dysfunction: elevated liver enzymes indicating possible liver injury.
  • Hematologic abnormalities: rare cases of blood cell count changes.

Precautions & Warnings

When prescribing ebastine, several safety considerations should be observed.

  • Pregnancy: use only if the potential benefit justifies the potential risk; consult a healthcare professional.
  • Breastfeeding: weigh benefits against possible effects on the infant; monitor infant for adverse reactions.
  • Elderly patients: monitor for increased sedation or dizziness due to age‑related pharmacokinetic changes.
  • Renal or hepatic impairment: consider dose adjustment or increased monitoring in patients with reduced organ function.
  • Concomitant medications: review for potential interactions, especially with CYP3A4 inhibitors.
  • Store at ambient temperature: keep tablets below 25 °C in the original packaging, protected from moisture.

Avoid Interactions

Ebastine may interact with other medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Ketoconazole: strong CYP3A4 inhibition can raise ebastine plasma levels, increasing risk of side effects.
  • Ritonavir: potent CYP3A4 inhibitor may lead to excessive ebastine exposure.
  • Erythromycin: CYP3A4 inhibition may elevate ebastine concentrations.

Moderate Interactions (Monitor Closely)

  • First‑generation antihistamines: additive sedation when combined with ebastine.
  • Alcohol: may enhance drowsiness and impair coordination.
  • Theophylline: possible alteration of ebastine metabolism requiring monitoring.

Frequently Asked Questions

Kestine 20 contains ebastine, a second‑generation antihistamine indicated for the relief of symptoms associated with allergic rhinitis and chronic idiopathic urticaria. It helps reduce itching, sneezing, nasal congestion and hives caused by histamine release.

Ebastine selectively blocks peripheral H1 histamine receptors, preventing histamine from binding to these sites on mast cells, blood vessels and nerves. This inhibition reduces vasodilation, increased vascular permeability and nerve stimulation, thereby alleviating typical allergic symptoms.

The exact dose of Kestine 20 is determined by the prescribing healthcare professional based on the patient’s condition, age and response. In clinical practice, a common regimen is one 20 mg tablet taken once daily, but the prescriber may adjust the regimen as needed.

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

To order Kestine 20, 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. The sales team then provides pricing, availability, shipping details and any necessary import documentation.

Compared with first‑generation antihistamines, ebastine (Kestine 20) offers a lower risk of sedation and central nervous system effects because it does not readily cross the blood‑brain barrier. Its once‑daily dosing and long half‑life provide convenient symptom control, while efficacy in allergic rhinitis and urticaria is comparable to other second‑generation agents.

Kestine 20 tablets should be stored at ambient temperature, preferably below 25 °C. Keep them in the original blister pack or container, protect from moisture and direct sunlight, and keep out of reach of children.

Kestine 20 is taken orally with or without food. The tablet should be swallowed whole with a glass of water. Patients should follow the dosing instructions provided by their prescriber and avoid crushing or chewing the tablet unless instructed otherwise.

Serious adverse reactions, although rare, include angioedema, severe skin reactions such as Stevens‑Johnson syndrome, cardiac arrhythmias due to QT prolongation, anaphylaxis, hepatic dysfunction and significant hematologic changes. Any signs of swelling, rash, difficulty breathing or unusual fatigue should prompt immediate medical attention.

Kestine 20 should be avoided in individuals with known hypersensitivity to ebastine or any of the tablet’s excipients. Caution is advised for patients with severe hepatic impairment, known QT prolongation, or those taking strong CYP3A4 inhibitors. Pregnant or breastfeeding women should only use it after consulting a healthcare professional.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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