Product image of Keral (Dexketoprofen) supplied by GNH India

Keral

Active Ingredient:
Dexketoprofen
Origin:
EU

Keral (Dexketoprofen)

Dexketoprofen, the active ingredient in Keral, is a nonsteroidal anti‑inflammatory drug presented as an oral formulation for systemic use. It is indicated for the relief of mild to moderate pain, including musculoskeletal, post‑operative and dysmenorrhea pain, in adult patients.

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

Manufacturer / TM Owner

Menarini International Operations Luxembourg S.A.

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Indications & Clinical Uses

Dexketoprofen acts as an NSAID to reduce pain and inflammation in several clinical settings.

  • Mild to moderate pain: provides rapid analgesia for everyday pain conditions.
  • Musculoskeletal pain: decreases inflammation and improves mobility in joint and muscle disorders.
  • Post‑operative pain: alleviates surgical discomfort during the recovery period.
  • Dysmenorrhea: relieves menstrual cramps and associated discomfort.

How It Works

  • Dexketoprofen inhibits cyclo‑oxygenase (COX‑1 and COX‑2) enzymes, which blocks the conversion of arachidonic acid to prostaglandins. By reducing prostaglandin synthesis, it diminishes peripheral sensitisation, inflammation, and pain signalling at the site of tissue injury, resulting in analgesic and anti‑inflammatory effects.

Side Effects

Adverse reactions may range from mild to serious and should be monitored during therapy.

Common Side Effects

  • Gastro‑intestinal discomfort: nausea, dyspepsia or abdominal pain.
  • Headache: mild to moderate intensity.
  • Dizziness or vertigo.
  • Skin rash: mild erythema or pruritus.
  • Elevated blood pressure: transient increase.
  • Mild renal function changes.

Serious or Rare Side Effects

  • Gastro‑intestinal ulceration or bleeding.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Acute renal failure or significant creatinine rise.
  • Hepatic injury: hepatitis or liver enzyme elevation.
  • Anaphylactic or anaphylactoid reactions.
  • Cardiovascular events: myocardial infarction or stroke in high‑risk patients.

Precautions & Warnings

Before initiating therapy, consider the following safety measures.

  • Renal assessment: evaluate kidney function, especially in elderly or dehydrated patients.
  • Hepatic assessment: check liver enzymes if pre‑existing liver disease is present.
  • Hypersensitivity: avoid use in individuals with known allergy to dexketoprofen or other NSAIDs.
  • Anticoagulant use: monitor bleeding risk when combined with warfarin or similar agents.
  • Blood pressure monitoring: watch for hypertension in patients with cardiovascular risk.
  • Store at ambient temperature: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Dexketoprofen may interact with several drug classes; some require avoidance while others need close monitoring.

Major Interactions (Avoid)

  • Anticoagulants (e.g., warfarin): increased risk of serious bleeding.
  • ACE inhibitors or ARBs: heightened chance of renal impairment.
  • Lithium: NSAIDs can raise lithium serum levels, risking toxicity.
  • Methotrexate: reduced clearance may lead to toxicity.

Moderate Interactions (Monitor Closely)

  • Other NSAIDs or COX‑2 inhibitors: additive gastrointestinal toxicity.
  • Selective serotonin reuptake inhibitors (SSRIs): elevated bleeding tendency.
  • Diuretics: possible reduction in renal perfusion, requiring renal function monitoring.

Frequently Asked Questions

Keral contains dexketoprofen, an NSAID indicated for the relief of mild to moderate pain such as musculoskeletal discomfort, post‑operative pain, and dysmenorrhea. It works by reducing inflammation and pain signalling, making it suitable for adult patients needing short‑term analgesia.

Dexketoprofen blocks cyclo‑oxygenase enzymes (COX‑1 and COX‑2), which are responsible for producing prostaglandins that mediate inflammation and pain. By lowering prostaglandin levels, the drug reduces peripheral sensitisation, leading to decreased pain perception and swelling at the affected site.

The specific dosage of Keral is determined by the prescribing clinician based on the patient’s condition, age, weight, and overall health. Healthcare professionals follow local prescribing guidelines and adjust the dose to achieve effective pain control while minimising risk.

The safety of dexketoprofen in pregnancy and lactation has not been definitively established. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and this decision must be made by a qualified healthcare provider.

To request Keral, 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.

Dexketoprofen is the active enantiomer of ketoprofen, offering rapid onset of analgesia with a potentially lower gastrointestinal side‑effect profile compared with some non‑selective NSAIDs. However, individual response varies, and clinicians consider efficacy, safety, patient history and drug‑interaction potential when selecting an NSAID.

Keral should be stored at ambient temperature, below 25 °C. Keep the tablets in the original container, protect them from moisture and direct sunlight, and ensure they are out of reach of children.

Keral is taken orally, usually with a glass of water. It can be taken with or without food, but patients who experience gastrointestinal discomfort may benefit from taking it with a meal or a snack, as advised by their prescriber.

Serious risks include gastrointestinal ulceration or bleeding, severe skin reactions such as Stevens‑Johnson syndrome, acute renal failure, hepatic injury, and increased cardiovascular events in high‑risk individuals. Patients should seek immediate medical attention if they notice signs of these conditions.

Keral is contraindicated in patients with known hypersensitivity to dexketoprofen or other NSAIDs, those with active gastrointestinal bleeding or ulcer disease, severe renal or hepatic impairment, and individuals who have had a recent coronary artery bypass graft surgery. A healthcare professional should evaluate suitability before prescribing.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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