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 an oral tablet for oral use. It provides analgesic and anti‑inflammatory effects for mild to moderate pain, including musculoskeletal, postoperative and dental pain, and is commonly prescribed for acute pain management in adult patients.

GNH India supplies Ketesse as a licensed, GDP‑compliant international pharmaceutical supplier, providing quality‑assured medicines to hospitals, pharmacies and clinics worldwide, with adherence to EU GMP standards and reliable logistics. The company ensures compliance with international regulatory requirements and offers flexible shipment options to meet diverse market needs.

Manufacturer / TM Owner

Menarini International Operations Luxembourg S.A.

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Indications & Clinical Uses

Dexketoprofen is used to relieve acute pain by inhibiting inflammatory pathways associated with musculoskeletal, postoperative, dental and other short‑term painful conditions.

  • Musculoskeletal pain: provides analgesic relief for acute or chronic musculoskeletal conditions.
  • Postoperative pain: reduces pain intensity after surgical procedures.
  • Dental pain: alleviates pain following dental extractions or procedures.
  • Dysmenorrhea: reduces menstrual cramps and associated pain.
  • Acute low back pain: provides rapid analgesia for sudden low back discomfort.
  • Rheumatic pain: helps control mild pain in rheumatic disorders.
  • Post‑traumatic pain: eases pain after minor injuries.

How It Works

  • Dexketoprofen exerts its effect by reversibly inhibiting cyclooxygenase‑1 (COX‑1) and cyclooxygenase‑2 (COX‑2) enzymes, which reduces the synthesis of prostaglandins involved in pain, inflammation and fever. The selective blockade of COX enzymes diminishes peripheral sensitisation of nociceptors, leading to analgesia and anti‑inflammatory activity without directly affecting central nervous system pathways. The rapid onset of action is due to its high bioavailability after oral administration, allowing effective pain control within 30 minutes.

Side Effects

Dexketoprofen may cause adverse reactions, which are classified by frequency and severity.

Common Side Effects

  • Nausea: mild to moderate upset stomach.
  • Dyspepsia: discomfort or burning in the upper abdomen.
  • Headache: transient pain in the head region.
  • Dizziness: sensation of light‑headedness or unsteadiness.

Serious or Rare Side Effects

  • Gastrointestinal bleeding or ulceration: potentially life‑threatening bleeding in the stomach or intestines.
  • Renal impairment: reduced kidney function, especially in at‑risk patients.
  • Severe skin reactions: such as Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Anaphylaxis: rare but severe allergic reaction requiring immediate medical attention.

Precautions & Warnings

When prescribing or dispensing Dexketoprofen, consider the following precautions to minimise risk.

  • Assess renal function: evaluate kidney status before initiating therapy, especially in elderly patients.
  • Assess hepatic function: monitor liver enzymes in patients with pre‑existing liver disease.
  • Use lowest effective dose: prescribe the minimal dose needed for pain control.
  • Avoid in known hypersensitivity: discontinue if allergic reactions occur.
  • Caution with anticoagulants: monitor bleeding risk when combined with warfarin or antiplatelet agents.
  • Store at ambient temperature: keep in the original packaging, protect from moisture and heat.

Avoid Interactions

Dexketoprofen can interact with other medicines; some combinations should be avoided while others require careful monitoring.

Major Interactions (Avoid)

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

Moderate Interactions (Monitor Closely)

  • Diuretics: may reduce renal clearance of dexketoprofen.
  • ACE inhibitors or ARBs: potential for reduced renal function.

Frequently Asked Questions

Ketesse contains dexketoprofen, an NSAID indicated for the relief of mild to moderate pain. It is commonly prescribed for musculoskeletal discomfort, postoperative pain after surgery, dental pain following dental procedures, dysmenorrhea, acute low‑back pain, rheumatic pain and pain that follows minor injuries.

Dexketoprofen works by reversibly inhibiting the cyclooxygenase‑1 (COX‑1) and cyclo‑oxygenase‑2 (COX‑2) enzymes. This inhibition reduces the production of prostaglandins, which are mediators of inflammation, pain and fever, thereby providing analgesic and anti‑inflammatory effects at the site of injury.

The appropriate dose of Ketesse is determined by the prescribing healthcare professional based on the individual’s pain severity, age, renal and hepatic function, and other clinical factors. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety data for dexketoprofen in pregnancy and lactation are limited. It is generally advised to avoid NSAIDs, including dexketoprofen, during the third trimester and to discuss potential risks with a healthcare provider before using the product while pregnant or breastfeeding.

To order Ketesse, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies 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 a single‑enantiomer NSAID that often provides faster onset of analgesia compared with traditional ibuprofen or naproxen. Its potency allows lower dosing for comparable pain relief, but the safety profile regarding gastrointestinal and renal effects remains similar to other NSAIDs.

Ketesse should be stored at ambient temperature, below 25 °C. Keep the tablets in the original container, protect them from moisture and direct heat, and ensure the packaging remains tightly closed until use.

Ketesse is administered orally, usually as a tablet that is swallowed whole with a glass of water. It is taken with or without food, according to the prescriber’s guidance, and the dosing interval is set by the treating clinician.

The most serious risks include gastrointestinal bleeding or ulceration, severe renal impairment, hypersensitivity reactions such as anaphylaxis, and rare but life‑threatening skin conditions like Stevens‑Johnson syndrome. Patients should seek immediate medical attention if they experience signs of these events.

Ketesse should be avoided in individuals with known hypersensitivity to dexketoprofen or other NSAIDs, those with active gastrointestinal ulcers, severe heart failure, uncontrolled hypertension, significant renal or hepatic impairment, and in patients receiving anticoagulant therapy unless closely monitored.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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