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 treats mild to moderate pain, including musculoskeletal, post‑operative and dental pain, in adult patients.

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 reduces pain and inflammation by inhibiting cyclooxygenase enzymes.

  • Mild to moderate pain: provides analgesia for general pain conditions.
  • Musculoskeletal pain: alleviates pain associated with muscles, joints and soft tissues.
  • Post‑operative pain: helps control pain after surgical procedures.
  • Dental pain: reduces pain following dental interventions.

How It Works

  • Dexketoprofen exerts its effect by non‑selectively inhibiting cyclooxygenase‑1 and cyclooxygenase‑2 enzymes, which decreases the conversion of arachidonic acid to prostaglandins. The reduced prostaglandin synthesis leads to diminished inflammation, pain perception, and fever responses at the site of tissue injury.

Side Effects

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

Common Side Effects

  • Gastrointestinal discomfort: nausea, dyspepsia, or abdominal pain.
  • Headache: mild to moderate intensity.
  • Dizziness: transient sensation of light‑headedness.
  • Rash: mild skin irritation or erythema.
  • Elevated liver enzymes: transient increase in hepatic markers.

Serious or Rare Side Effects

  • Gastrointestinal ulcer or bleeding: potentially life‑threatening hemorrhage.
  • Renal impairment: reduced kidney function or acute kidney injury.
  • Severe allergic reactions: anaphylaxis, angioedema, or Stevens‑Johnson syndrome.
  • Hepatic dysfunction: hepatitis or liver failure.
  • Cardiovascular events: increased risk of myocardial infarction or stroke.

Precautions & Warnings

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

  • Assess gastrointestinal risk: review history of ulcers, bleeding disorders, or chronic NSAID use.
  • Evaluate renal function: check baseline creatinine and monitor during therapy, especially in the elderly.
  • Monitor hepatic status: perform liver function tests if pre‑existing liver disease is present.
  • Caution in cardiovascular disease: consider alternative analgesics for patients with recent myocardial infarction or uncontrolled hypertension.
  • Avoid in known hypersensitivity: discontinue if signs of severe allergic reaction appear.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, and protect from moisture.

Avoid Interactions

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

Major Interactions (Avoid)

  • Other NSAIDs or aspirin: heightened risk of gastrointestinal bleeding.
  • Anticoagulants (e.g., warfarin, DOACs): increased bleeding tendency.
  • Selective COX‑2 inhibitors: additive renal and cardiovascular hazards.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or diuretics: potential reduction in renal function.
  • Lithium: NSAIDs can raise lithium serum concentrations.
  • Methotrexate: reduced clearance may lead to toxicity.

Frequently Asked Questions

Ketesse, containing dexketoprofen, is indicated for the relief of mild to moderate pain such as musculoskeletal discomfort, post‑operative pain, and dental pain. It is prescribed for adult patients who need short‑term analgesia and anti‑inflammatory effects.

Dexketoprofen works by non‑selectively inhibiting the cyclooxygenase‑1 and cyclooxygenase‑2 enzymes, which reduces the synthesis of prostaglandins. Lower prostaglandin levels diminish inflammation and the transmission of pain signals, providing analgesic and anti‑inflammatory benefits.

The exact dosage of Ketesse is determined by the prescribing healthcare professional based on the patient’s condition, age, weight, and overall health. The prescriber will set the appropriate dose and dosing interval according to clinical guidelines.

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 only under medical supervision.

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 with a potentially lower gastrointestinal side‑effect profile compared with some non‑selective NSAIDs. However, its overall safety and efficacy are comparable to other NSAIDs, and choice depends on individual patient factors and clinical judgment.

Ketesse should be stored at ambient temperature, preferably 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.

Ketesse is taken orally, usually with a full glass of water. It may be taken with or without food, but taking it with food can reduce the likelihood of gastrointestinal discomfort. Follow the prescribing clinician’s instructions for timing and frequency.

Serious risks include gastrointestinal ulceration or bleeding, renal impairment, severe allergic reactions such as anaphylaxis, and cardiovascular events like myocardial infarction or stroke. Patients should be monitored for these events, especially if they have pre‑existing risk factors.

Ketesse should be avoided in patients with known hypersensitivity to dexketoprofen or other NSAIDs, active gastrointestinal ulcer or bleeding, severe renal or hepatic impairment, and in those with uncontrolled hypertension or recent cardiovascular events unless specifically advised by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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