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 nonsteroidal anti-inflammatory drug (NSAID) presented as a parenteral formulation for intramuscular and intravenous use. It provides rapid analgesic and anti‑inflammatory effects for mild‑to‑moderate acute pain in adult patients, including postoperative and musculoskeletal pain.

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 used to manage pain and inflammation within the musculoskeletal and postoperative domains.

  • Post‑operative pain: reduces pain intensity after surgical procedures.
  • Musculoskeletal pain: alleviates pain associated with strains, sprains, and back pain.
  • Acute inflammatory conditions: diminishes inflammation and discomfort in conditions such as acute gout attacks.

How It Works

  • Dexketoprofen exerts its effect by reversibly inhibiting cyclooxygenase‑1 (COX‑1) and cyclooxygenase‑2 (COX‑2) enzymes, blocking the conversion of arachidonic acid to prostaglandins. The resulting reduction in prostaglandin synthesis decreases nociceptor sensitisation and attenuates inflammatory responses, providing analgesic and anti‑inflammatory activity at the site of tissue injury.

Side Effects

Dexketoprofen may be associated with a range of adverse reactions, which are categorised by frequency and severity.

Common Side Effects

  • Nausea: mild to moderate upset stomach.
  • Dizziness: transient light‑headedness.
  • Headache: mild to moderate intensity.
  • Injection site pain: local discomfort at the administration site.
  • Gastrointestinal discomfort: dyspepsia or mild abdominal pain.
  • Transient increase in blood pressure.

Serious or Rare Side Effects

  • Severe gastrointestinal bleeding or ulceration.
  • Anaphylactic or severe allergic reactions.
  • Acute renal impairment or failure.
  • Hepatic dysfunction or elevated liver enzymes.
  • Cardiovascular thrombotic events such as myocardial infarction.
  • Stevens‑Johnson syndrome or toxic epidermal necrolysis.

Precautions & Warnings

When prescribing Dexketoprofen, clinicians should consider several safety aspects.

  • Renal function: assess baseline renal status and monitor during therapy.
  • Gastrointestinal risk: avoid in patients with active ulcer disease or a history of GI bleeding.
  • Cardiovascular caution: use cautiously in patients with hypertension or established heart disease.
  • Bleeding tendency: monitor coagulation parameters if combined with anticoagulants.
  • Pregnancy and lactation: evaluate risk–benefit; use only if clearly needed.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze.

Avoid Interactions

Dexketoprofen can interact with other medicines, requiring attention to the level of risk.

Major Interactions (Avoid)

  • Anticoagulants (e.g., warfarin): increased risk of bleeding.
  • Other NSAIDs or COX‑2 inhibitors: additive gastrointestinal toxicity.
  • Selective serotonin reuptake inhibitors (SSRIs): heightened hemorrhage risk.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or diuretics: possible reduction in renal function.
  • Lithium: NSAIDs may raise lithium serum concentrations.
  • Methotrexate: decreased clearance leading to potential toxicity.

Frequently Asked Questions

Ketesse, containing dexketoprofen, is indicated for the relief of mild to moderate acute pain such as postoperative discomfort, musculoskeletal pain from strains or sprains, and pain associated with acute inflammatory conditions like gout attacks.

Dexketoprofen works by reversibly blocking the COX‑1 and COX‑2 enzymes, which reduces the production of prostaglandins. Lower prostaglandin levels diminish inflammation and decrease the sensitivity of pain‑receiving nerves, providing analgesic and anti‑inflammatory effects.

The specific dose of Ketesse is determined by the prescribing clinician based on the patient’s condition, weight, renal function and other clinical factors. Only a qualified health professional should set the dosing regimen.

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 after a thorough risk‑benefit assessment by the prescriber.

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.

Dexketoprofen is the S‑enantiomer of ketoprofen, offering a faster onset of analgesia compared with many traditional NSAIDs. Its potency allows lower dosing for comparable pain relief, but the overall safety profile remains similar to other NSAIDs, requiring attention to gastrointestinal, renal and cardiovascular risks.

Ketesse should be stored at 2‑8 °C, kept refrigerated, protected from light, and must not be frozen or shaken. Maintaining the cold‑chain ensures the stability and sterility of the injectable product.

Ketesse is supplied as a sterile injectable solution for intramuscular or intravenous administration. The route, injection site and infusion rate are determined by the treating physician according to the clinical situation.

Serious risks include severe gastrointestinal bleeding or ulceration, anaphylactic reactions, acute renal failure, hepatic injury, and cardiovascular events such as myocardial infarction or stroke. Patients should be monitored closely for these events, especially if risk factors are present.

Ketesse is contraindicated in patients with known hypersensitivity to dexketoprofen or other NSAIDs, active gastrointestinal ulceration, severe renal or hepatic impairment, and in individuals with established cardiovascular disease where NSAID use is discouraged. The prescriber must evaluate each patient’s medical history before initiating therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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