Product image of Keal (Sucralfate) supplied by GNH India

Keal

Active Ingredient:
Sucralfate
Origin:
EU

Keal (Sucralfate)

Sucralfate, the active ingredient in Keal, is a mucosal protective agent presented as an oral formulation for oral use. It treats duodenal and gastric ulcers and helps manage gastro‑oesophageal reflux disease in adult patients.
GNH India supplies Keal as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Exod

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Indications & Clinical Uses

Sucralfate acts on the gastrointestinal mucosa to protect ulcerated tissue and reduce reflux injury.

  • Duodenal ulcer: promotes healing by shielding the ulcer base from acid and pepsin.
  • Gastric ulcer: forms a protective barrier that facilitates mucosal repair.
  • Gastro‑oesophageal reflux disease (GERD): reduces mucosal irritation by limiting exposure to gastric contents.

How It Works

  • Sucralfate binds to ulcer exudate and mucosal proteins, creating a viscous, adherent coating that isolates the lesion from gastric acid, pepsin, and bile salts. The coating also stimulates local prostaglandin synthesis and mucus production, enhancing mucosal defense and promoting ulcer healing.

Side Effects

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

Common Side Effects

  • Constipation: mild to moderate difficulty passing stool.
  • Dry mouth: reduced salivary flow.
  • Nausea: transient feeling of queasiness.
  • Indigestion: mild dyspeptic symptoms.
  • Flatulence: increased intestinal gas.
  • Taste alteration: temporary metallic or bitter taste.

Serious or Rare Side Effects

  • Severe constipation leading to bowel obstruction.
  • Allergic reactions: rash, itching, or swelling.
  • Hypersensitivity: anaphylaxis in rare cases.
  • Hypermagnesemia: elevated magnesium levels, especially with renal impairment.
  • Severe abdominal pain: may indicate complications.
  • Persistent vomiting: could signal intolerance or obstruction.

Precautions & Warnings

Before prescribing Sucralfate, consider patient-specific factors and safety measures.

  • Renal impairment: monitor magnesium levels and adjust use if needed.
  • Gastrointestinal obstruction: avoid use in patients with known obstruction or severe constipation.
  • Drug absorption: administer on an empty stomach, separate from other oral medications by at least 2 hours.
  • Pregnancy and lactation: use only if the potential benefit outweighs risk, as safety data are limited.
  • Elderly patients: start with caution due to higher risk of constipation and renal issues.
  • Store at ambient temperature: keep below 25°C, retain in original packaging, and protect from moisture.

Avoid Interactions

Sucralfate can affect the absorption of several concomitant drugs.

Major Interactions (Avoid)

  • Antibiotics (e.g., quinolones, tetracyclines): may reduce their bioavailability.
  • Antifungal agents (e.g., fluconazole): absorption can be markedly decreased.
  • Iron supplements: binding reduces iron absorption.

Moderate Interactions (Monitor Closely)

  • Digoxin: potential reduction in absorption; monitor serum levels.
  • Levothyroxine: may decrease absorption; check thyroid function.
  • Antacids containing aluminum or magnesium: may interfere with Sucralfate binding; separate dosing times.

Frequently Asked Questions

Keal, containing the active ingredient Sucralfate, is prescribed for the treatment of duodenal ulcers, gastric ulcers, and gastro‑oesophageal reflux disease (GERD). It works by protecting the ulcerated mucosa and reducing irritation from stomach acid.

Sucralfate adheres to ulcer exudate and mucosal proteins, forming a protective barrier that shields the lesion from acid, pepsin, and bile salts. This barrier also stimulates prostaglandin synthesis and mucus production, enhancing the natural defense mechanisms of the gastrointestinal lining.

The dosage of Keal is determined by the prescribing healthcare professional based on the patient’s specific condition, severity, and response to therapy. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety data for Sucralfate in pregnancy and lactation are limited. It 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 request Keal, 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.

Keal (Sucralfate) differs from acid‑suppressing agents such as proton‑pump inhibitors or H2‑receptor antagonists. While those drugs reduce gastric acid production, Sucralfate protects the ulcer surface directly and promotes mucosal healing without altering acid secretion.

Keal should be stored at ambient temperature, preferably below 25 °C. Keep the product in its original packaging, protect it from moisture, and store it out of direct sunlight to maintain stability.

Keal is taken orally, usually on an empty stomach. It should be swallowed with a full glass of water, and other oral medicines should be spaced at least two hours apart to avoid interference with absorption.

Serious risks, though rare, include severe constipation leading to bowel obstruction, allergic reactions such as rash or anaphylaxis, and hypermagnesemia in patients with renal impairment. Patients should seek immediate medical attention if they experience these symptoms.

Keal is contraindicated in patients with known hypersensitivity to Sucralfate or any of its excipients, and it should be used with caution in individuals with renal failure, gastrointestinal obstruction, or severe constipation.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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