Product image of Ketospray (Ketoprofen) supplied by GNH India

Ketospray

Active Ingredient:
Ketoprofen
Origin:
EU

Ketospray (Ketoprofen)

Ketoprofen, the active ingredient in Ketospray, is a Nonsteroidal anti‑inflammatory drug (NSAID) presented as a topical spray for cutaneous use. It is employed to relieve pain and reduce inflammation in localized musculoskeletal conditions and is suitable for adult patients who require topical therapy.

GNH India supplies Ketospray as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

G.T.S. Solution S.R.L.

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Indications & Clinical Uses

Ketoprofen acts locally on inflammatory pathways to provide analgesic and anti‑inflammatory effects for several musculoskeletal conditions.

  • Musculoskeletal pain: reduces pain intensity in strained muscles and joints.
  • Tendinitis and bursitis: diminishes inflammation and improves mobility.
  • Sprains and strains: alleviates swelling and discomfort after minor injuries.
  • Osteoarthritis of superficial joints: provides topical relief of pain and stiffness.

How It Works

  • Ketoprofen inhibits cyclooxygenase (COX‑1 and COX‑2) enzymes in peripheral tissues, leading to decreased synthesis of prostaglandins that mediate pain, fever, and inflammation. By limiting prostaglandin production at the site of application, the drug reduces vascular permeability, edema, and nociceptor sensitisation, resulting in localized analgesic and anti‑inflammatory effects.

Side Effects

Ketoprofen spray may cause local and systemic adverse reactions, most of which are mild and reversible.

Common Side Effects

  • Skin irritation: mild burning or stinging at the application site.
  • Redness: localized erythema.
  • Itching: pruritus around the treated area.
  • Dryness: transient dryness of the skin.
  • Rash: mild maculopapular eruption.
  • Swelling: slight edema at the site of use.

Serious or Rare Side Effects

  • Allergic reactions: urticaria, angio‑edema, or anaphylaxis.
  • Severe skin disorders: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Systemic NSAID effects: gastrointestinal ulceration or bleeding.
  • Renal impairment: reduced kidney function with prolonged use.
  • Hepatic dysfunction: elevated liver enzymes or hepatitis.
  • Blood disorders: thrombocytopenia or leukopenia.

Precautions & Warnings

When using Ketospray, consider the following safety measures.

  • Hypersensitivity: avoid if the patient has known allergy to ketoprofen or other NSAIDs.
  • Gastrointestinal risk: do not use in patients with active peptic ulcer disease or severe GI bleeding.
  • Renal or hepatic impairment: use with caution and monitor function.
  • Concomitant NSAIDs: avoid simultaneous use with other topical or systemic NSAIDs to reduce toxicity.
  • Pregnancy and lactation: use only if the prescriber determines potential benefits outweigh risks.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Ketoprofen may interact with several medicines; some combinations should be avoided while others require monitoring.

Major Interactions (Avoid)

  • Anticoagulants (e.g., warfarin): increased risk of bleeding.
  • Other NSAIDs or COX‑2 inhibitors: additive gastrointestinal and renal toxicity.
  • Corticosteroids: heightened risk of ulceration and bleeding.

Moderate Interactions (Monitor Closely)

  • Diuretics (e.g., furosemide): may reduce renal perfusion; monitor kidney function.
  • Lithium: NSAIDs can raise lithium levels; check serum concentrations.
  • Methotrexate: reduced clearance may increase toxicity; monitor hepatic and renal parameters.

Frequently Asked Questions

Ketospray contains ketoprofen, a topical NSAID that is applied to the skin to relieve localized pain and reduce inflammation associated with musculoskeletal conditions such as sprains, strains, tendinitis, and superficial osteoarthritis.

Ketoprofen inhibits cyclooxygenase enzymes (COX‑1 and COX‑2) in the skin, decreasing the production of prostaglandins that cause pain, swelling, and redness. This localized inhibition provides analgesic and anti‑inflammatory effects at the site of application.

The specific dose and frequency of Ketospray are determined by the prescribing healthcare professional based on the patient’s condition, age, and response to therapy. Patients should follow the prescriber’s instructions and the product label.

Safety of topical ketoprofen in pregnancy or lactation has not been definitively established. It should only be used if the prescriber judges that the potential benefit outweighs any possible risk to the mother or infant.

To request Ketospray, 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.

Ketospray delivers ketoprofen directly to the skin, providing targeted relief with lower systemic exposure compared with oral tablets. This can reduce the risk of gastrointestinal and renal side effects, but it is limited to superficial conditions rather than widespread pain.

Store Ketospray at room temperature, below 25 °C, in its original packaging. Keep the container tightly closed, protect it from moisture and direct sunlight, and keep it out of reach of children.

Ketospray is applied topically to clean, dry skin over the affected area. The prescribed amount is sprayed and gently massaged in, usually 2–4 times daily, or as directed by the healthcare professional.

Serious risks include severe allergic reactions such as anaphylaxis, Stevens‑Johnson syndrome, toxic epidermal necrolysis, and systemic NSAID effects like gastrointestinal bleeding, renal impairment, and hepatic injury, especially with prolonged or extensive use.

Ketospray should not be used by individuals with known hypersensitivity to ketoprofen or other NSAIDs, those with active peptic ulcer disease, severe renal or hepatic impairment, or by patients who are pregnant or breastfeeding unless specifically advised by a prescriber.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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