Product image of Ketum (Ketoprofen) supplied by GNH India

Ketum

Active Ingredient:
Ketoprofen
Origin:
EU

Ketum (Ketoprofen)

Ketoprofen, the active ingredient in Ketum, is a Nonsteroidal anti‑inflammatory drug (NSAID) presented as a topical formulation for external use. It is used to relieve pain and reduce inflammation in musculoskeletal conditions and is applied directly to the skin of affected areas.
GNH India supplies Ketum as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Menarini France

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Indications & Clinical Uses

Ketoprofen acts locally to alleviate pain and inflammation in the musculoskeletal system.

  • Musculoskeletal pain: provides topical analgesia and reduces discomfort in joints and muscles.
  • Soft‑tissue inflammation: diminishes swelling and erythema in sprains, strains and bruises.
  • Osteoarthritis of the knee: helps control pain and stiffness associated with degenerative joint disease.
  • Post‑operative superficial pain: eases localized discomfort after minor skin‑level procedures.

How It Works

  • Ketoprofen inhibits cyclooxygenase‑1 and cyclooxygenase‑2 (COX‑1, COX‑2) enzymes in peripheral tissues, leading to reduced synthesis of prostaglandins that mediate pain, fever and inflammation. By limiting prostaglandin production at the site of application, the drug decreases vascular permeability, edema, and nociceptor sensitisation, resulting in localized analgesic and anti‑inflammatory effects without substantial systemic exposure.

Side Effects

Ketum may cause skin‑related reactions and, rarely, systemic adverse events.

Common Side Effects

  • Local burning or stinging sensation at the application site.
  • Mild erythema or redness of the skin.
  • Itching or pruritus.
  • Dryness or peeling of the treated area.
  • Contact dermatitis limited to the area of use.

Serious or Rare Side Effects

  • Allergic contact dermatitis with extensive rash.
  • Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Systemic NSAID effects such as gastrointestinal ulceration.
  • Renal impairment or reduced kidney function.
  • Cardiovascular events including hypertension or thrombotic episodes.

Precautions & Warnings

Before using Ketum, consider the following safety measures.

  • Hypersensitivity: avoid if you have known allergy to ketoprofen or other NSAIDs.
  • Broken skin: do not apply on open wounds, cuts or abrasions.
  • Cardiovascular risk: use with caution in patients with heart disease or hypertension.
  • Renal or hepatic impairment: monitor function and limit duration of use.
  • Concomitant NSAIDs: avoid using other topical or oral NSAIDs simultaneously.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Ketum can interact with other medicines, requiring attention to avoid adverse outcomes.

Major Interactions (Avoid)

  • Oral anticoagulants (e.g., warfarin): increased bleeding risk.
  • Other NSAIDs or aspirin: heightened gastrointestinal toxicity.
  • Systemic corticosteroids: amplified ulcer risk.
  • Lithium therapy: potential increase in lithium levels.
  • Methotrexate: enhanced methotrexate toxicity.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or ARBs: possible reduction in renal function.
  • Diuretics: may affect electrolyte balance.
  • Selective serotonin reuptake inhibitors (SSRIs): modest increase in bleeding tendency.
  • Antihypertensive agents: potential attenuation of blood‑pressure control.
  • Beta‑blockers: monitor for any change in cardiovascular response.

Frequently Asked Questions

Ketum is a topical formulation containing ketoprofen, an NSAID that is applied to the skin to relieve pain and reduce inflammation associated with musculoskeletal disorders, soft‑tissue injuries, and osteoarthritis of the knee.

Ketoprofen blocks the cyclooxygenase‑1 and cyclooxygenase‑2 enzymes in peripheral tissues, decreasing the production of prostaglandins that cause pain, swelling, and fever. This local inhibition leads to analgesic and anti‑inflammatory effects at the site of application.

The specific amount of Ketum to apply and the frequency of use are determined by the prescribing healthcare professional based on the condition being treated, the size of the affected area, and individual patient factors.

Safety of topical ketoprofen during pregnancy or lactation has not been fully established. Women who are pregnant, planning to become pregnant, or breastfeeding should discuss potential risks and benefits with their physician before using Ketum.

To request Ketum, 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.

Ketum delivers ketoprofen, which has a slightly higher COX‑2 selectivity than some other topical NSAIDs such as diclofenac. This may provide effective pain relief with a comparable safety profile, but the choice of product should be guided by clinical response, tolerability and physician preference.

Ketum should be stored at room temperature, below 25 °C, in its original packaging. Keep the container tightly closed, protect it from moisture, direct sunlight and excessive heat to maintain product stability.

Ketum is applied topically to clean, dry skin over the affected area. The prescribed amount is spread in a thin layer and gently massaged until fully absorbed, usually two to four times daily, as directed by the prescriber.

Serious risks include severe allergic reactions such as Stevens‑Johnson syndrome, systemic NSAID effects like gastrointestinal ulceration, renal impairment, and cardiovascular events. Patients should seek immediate medical attention if they notice widespread rash, blistering, severe stomach pain, or signs of bleeding.

Ketum should not be used by individuals with a known hypersensitivity to ketoprofen or any NSAID, those with open wounds or infected skin at the application site, and patients with a history of severe cardiovascular, renal or hepatic disease unless specifically advised by a healthcare professional.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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