Product image of Ketesse (Dexketoprofen) supplied by GNH India

Ketesse

Active Ingredient:
Dexketoprofen
Origin:
EU

Ketesse (Dexketoprofen)

Dexketoprofen, the active ingredient in Ketesse, is a non‑steroidal anti‑inflammatory drug (NSAID) presented as an oral tablet for oral use. It is indicated for the relief of mild to moderate pain and for reducing inflammation in various conditions.
GNH India supplies Ketesse 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 is an NSAID that acts on the cyclooxygenase pathway to relieve pain and inflammation.

  • Mild to moderate pain: provides rapid analgesia for acute discomfort.
  • Musculoskeletal pain: reduces pain and swelling associated with strains, sprains and arthritis.
  • Post‑operative pain: helps control pain after surgical procedures.
  • Inflammatory conditions: diminishes inflammation in acute inflammatory states.

How It Works

  • Dexketoprofen exerts its effect by non‑selectively inhibiting cyclooxygenase‑1 (COX‑1) and cyclooxygenase‑2 (COX‑2) enzymes, which blocks the conversion of arachidonic acid to prostaglandins. The resulting decrease in prostaglandin synthesis reduces peripheral sensitisation of nociceptors, leading to analgesia, and limits the inflammatory cascade, providing anti‑inflammatory benefits.

Side Effects

Dexketoprofen may cause a range of adverse reactions, most of which are dose‑related and reversible.

Common Side Effects

  • Gastro‑intestinal discomfort: nausea, dyspepsia or abdominal pain.
  • Headache: mild to moderate intensity.
  • Dizziness or vertigo.
  • Mild skin rash or pruritus.
  • Elevated liver enzymes (transient).

Serious or Rare Side Effects

  • Gastro‑intestinal bleeding or ulceration.
  • Severe cardiovascular events such as myocardial infarction or stroke.
  • Acute renal failure or worsening of chronic kidney disease.
  • Severe skin reactions (Stevens‑Johnson syndrome, toxic epidermal necrolysis).
  • Anaphylactic or anaphylactoid reactions.
  • Hepatic necrosis or severe hepatitis.

Precautions & Warnings

Before prescribing Dexketoprofen, clinicians should evaluate patient‑specific risk factors and monitor for adverse events.

  • Gastro‑intestinal risk: assess history of ulcers or bleeding and consider gastro‑protective therapy.
  • Cardiovascular safety: review history of heart disease, hypertension or stroke.
  • Renal function: monitor creatinine and adjust use in patients with renal impairment.
  • Hepatic health: check liver enzymes in patients with liver disease.
  • Hypersensitivity: avoid in individuals with known allergy to dexketoprofen or other NSAIDs.
  • Store at room temperature: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Dexketoprofen can interact with several drug classes, altering efficacy or safety.

Major Interactions (Avoid)

  • Anticoagulants (e.g., warfarin): increased risk of bleeding.
  • Other NSAIDs or aspirin: additive gastrointestinal toxicity.
  • Lithium: elevated lithium levels leading to toxicity.
  • Methotrexate: reduced clearance and potential toxicity.
  • Selective serotonin reuptake inhibitors (SSRIs): heightened bleeding risk.

Moderate Interactions (Monitor Closely):\n- Antihypertensives (ACE inhibitors, ARBs, diuretics): possible reduction in antihypertensive effect.

  • Corticosteroids: increased risk of gastrointestinal ulceration.
  • Oral hypoglycemics: potential alteration of blood glucose control.
  • Diuretics: may affect renal function when combined.
  • Cyclosporine: increased nephrotoxicity risk.

Frequently Asked Questions

Ketesse, containing dexketoprofen, is used to treat mild to moderate pain, musculoskeletal pain such as strains or arthritis, post‑operative pain, and acute inflammatory conditions. It provides analgesic and anti‑inflammatory effects by reducing prostaglandin production.

Dexketoprofen works by non‑selectively inhibiting the cyclooxygenase‑1 and cyclooxygenase‑2 enzymes. This inhibition blocks the conversion of arachidonic acid to prostaglandins, which are mediators of pain, fever, and inflammation. The reduction in prostaglandin levels leads to analgesia and decreased inflammation.

The appropriate dose of Ketesse is determined by the prescribing healthcare professional based on the patient’s condition, age, weight, and overall health status. Dosage instructions are provided on the prescription label and should be followed exactly as directed.

The safety of dexketoprofen in pregnancy and lactation has not been fully 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 order Ketesse, 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.

Ketesse (dexketoprofen) is the S‑enantiomer of ketoprofen, offering rapid onset of analgesia and potentially lower gastrointestinal side‑effects compared with some non‑selective NSAIDs. Its efficacy is comparable to ibuprofen or diclofenac for acute pain, but individual response and safety profiles may vary.

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

Ketesse is taken orally, usually with a glass of water. It can be taken with or without food, but patients with a sensitive stomach may prefer to take it with meals to reduce gastrointestinal discomfort.

Serious risks include gastrointestinal bleeding or ulceration, cardiovascular events such as heart attack or stroke, severe renal impairment, and rare but life‑threatening skin reactions like Stevens‑Johnson syndrome. Patients should seek immediate medical attention if they experience symptoms such as severe abdominal pain, chest pain, sudden weakness, or skin rash.

Ketesse should be avoided in individuals with known hypersensitivity to dexketoprofen or other NSAIDs, active gastrointestinal ulceration or bleeding, severe heart failure, uncontrolled hypertension, and in patients with severe renal or hepatic impairment unless specifically directed by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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