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 injectable solution for intramuscular and intravenous use. It is indicated for moderate to severe acute pain, post‑operative pain and musculoskeletal 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 acts on inflammatory pathways to relieve pain in several clinical settings.

  • Moderate to severe acute pain: provides rapid analgesia for intense pain episodes.
  • Post‑operative pain: reduces pain after surgical procedures.
  • Musculoskeletal pain: alleviates pain associated with injuries or inflammatory conditions.

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 reduction in prostaglandin synthesis diminishes peripheral sensitisation, leading to decreased pain perception and inflammation at the site of injury.

Side Effects

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

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Headache: transient cranial discomfort.
  • Dizziness: occasional light‑headedness.
  • Injection site pain: local discomfort after administration.
  • Vomiting: occasional emesis.
  • Dyspepsia: indigestion or upper abdominal discomfort.

Serious or Rare Side Effects

  • Gastrointestinal bleeding: potentially life‑threatening hemorrhage.
  • Renal impairment: reduced kidney function, especially in at‑risk patients.
  • Severe allergic reactions: anaphylaxis, skin rash, or angioedema.
  • Cardiovascular events: increased risk of thrombotic events.
  • Liver enzyme elevation: signs of hepatic stress.
  • Hematologic abnormalities: rare blood dyscrasias.

Precautions & Warnings

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

  • Assess renal function: adjust use in patients with impaired kidney function.
  • Assess hepatic function: avoid in severe liver disease.
  • Avoid in known NSAID hypersensitivity: contraindicated for allergic individuals.
  • Use caution in cardiovascular disease: consider risk of thrombotic events.
  • Monitor for gastrointestinal ulcer risk: especially in patients with prior ulcer history.
  • Store at ambient temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Dexketoprofen may interact with several drug classes; awareness helps prevent harmful effects.

Major Interactions (Avoid)

  • Other NSAIDs: additive risk of gastrointestinal bleeding.
  • Anticoagulants (e.g., warfarin): increased bleeding tendency.
  • SSRIs or SNRIs: heightened risk of GI hemorrhage.
  • ACE inhibitors in renal‑compromised patients: possible renal function decline.

Moderate Interactions (Monitor Closely)

  • Diuretics: may affect renal clearance.
  • Lithium: potential for increased lithium levels.
  • Methotrexate: reduced clearance leading to toxicity.
  • Corticosteroids: synergistic ulcerogenic effect.
  • Antihypertensives: possible reduction in antihypertensive efficacy.

Frequently Asked Questions

Ketesse contains dexketoprofen, an NSAID indicated for the relief of moderate to severe acute pain, post‑operative pain, and musculoskeletal pain in adult patients. It is administered by injection to provide rapid analgesia in hospital or clinical settings.

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 peripheral sensitisation, resulting in decreased pain perception.

The specific dose and frequency of Ketesse are determined by the prescribing clinician based on the patient’s condition, severity of pain, and clinical judgment. Healthcare professionals should follow local prescribing guidelines and adjust as needed.

Safety data for dexketoprofen in pregnancy and lactation are limited. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and the decision must be made by a qualified healthcare provider.

To request 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 (including cold‑chain if required) and necessary import documentation.

Ketesse (dexketoprofen) is the S‑enantiomer of ketoprofen, offering a faster onset of analgesia and potentially lower gastrointestinal side‑effects compared with racemic ketoprofen. Compared with ibuprofen or diclofenac, dexketoprofen provides comparable pain relief at lower doses but shares similar class‑related risks.

Ketesse should be stored at ambient temperature, below 25 °C. Keep the vials in their original packaging, protect them from moisture and direct sunlight, and ensure the container remains sealed until use.

Ketesse is supplied as an injectable solution for intramuscular or intravenous administration. The route, injection site and infusion rate are determined by the prescribing clinician and should follow aseptic technique and local practice standards.

The most serious risks include gastrointestinal bleeding, severe allergic reactions (anaphylaxis), renal impairment, cardiovascular events such as myocardial infarction or stroke, and liver enzyme elevations. Patients should be monitored closely for these events, especially if they have pre‑existing risk factors.

Ketesse is contraindicated in patients with known hypersensitivity to dexketoprofen or other NSAIDs, active gastrointestinal ulceration, severe renal or hepatic impairment, and in those with established cardiovascular disease where NSAID use is discouraged. Clinicians should assess each patient individually.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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