Product image of Orudis (Ketoprofen) supplied by GNH India

Orudis

Active Ingredient:
Ketoprofen
Origin:
EU

Orudis (Ketoprofen)

Ketoprofen, the active ingredient in Orudis, is a non‑steroidal anti‑inflammatory drug presented as a 50 mg tablet for oral use. It relieves pain and inflammation associated with musculoskeletal disorders, osteoarthritis and rheumatoid arthritis in adults.

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

Manufacturer / TM Owner

Sanofi Oy

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Indications & Clinical Uses

Ketoprofen is an NSAID that reduces inflammation and pain in several musculoskeletal conditions.

  • Osteoarthritis: decreases joint pain and improves mobility.
  • Rheumatoid arthritis: lessens joint swelling and stiffness.
  • Ankylosing spondylitis: alleviates spinal pain and inflammation.
  • Acute musculoskeletal injury: provides short‑term pain relief and reduces swelling.
  • Post‑operative pain: helps control pain after minor surgical procedures.

How It Works

  • Ketoprofen inhibits cyclo‑oxygenase (COX‑1 and COX‑2) enzymes, reducing the synthesis of prostaglandins that mediate inflammation, pain and fever. By blocking these pathways, it diminishes peripheral sensitisation of nociceptors and lowers the inflammatory response in affected tissues.

Side Effects

Ketoprofen may cause a range of adverse reactions, most of which are mild and reversible.

Common Side Effects

  • Dyspepsia: mild stomach discomfort or heartburn.
  • Nausea: feeling of queasiness.
  • Headache: transient head pain.
  • Dizziness: light‑headed sensation.
  • Edema: mild swelling of the ankles or feet.

Serious or Rare Side Effects

  • Gastrointestinal ulcer or bleeding: severe stomach pain or black stools.
  • Renal impairment: reduced urine output or swelling.
  • Hepatotoxicity: jaundice or abnormal liver tests.
  • Severe skin reactions: rash, Stevens‑Johnson syndrome.
  • Anaphylaxis: sudden difficulty breathing or swelling of the face.

Precautions & Warnings

When using Ketoprofen, consider the following safety measures:

  • Assess renal function: check baseline creatinine in patients with kidney disease.
  • Monitor hepatic status: avoid use in active liver disease.
  • Evaluate cardiovascular risk: NSAIDs may increase thrombotic events.
  • Use gastro‑protective agents: consider PPIs for patients with ulcer history.
  • Avoid in late pregnancy: risk of fetal ductus arteriosus closure.
  • Store at below 25°C: keep in the original packaging, protect from moisture and light.

Avoid Interactions

Ketoprofen can interact with several medicines, altering efficacy or safety.

Major Interactions (Avoid)

  • Anticoagulants (e.g., warfarin): increased bleeding risk.
  • Selective serotonin reuptake inhibitors (SSRIs): heightened gastrointestinal bleeding.
  • ACE inhibitors / ARBs: may reduce renal perfusion.

Moderate Interactions (Monitor Closely)

  • Diuretics: potential for reduced kidney function.
  • Lithium: increased lithium levels.
  • Methotrexate: decreased clearance, raising toxicity risk.

Frequently Asked Questions

Orudis contains ketoprofen, an NSAID that is prescribed to relieve pain and inflammation associated with conditions such as osteoarthritis, rheumatoid arthritis, ankylosing spondylitis and acute musculoskeletal injuries. It is used in adults to improve mobility and reduce discomfort.

Ketoprofen works by inhibiting the cyclo‑oxygenase enzymes COX‑1 and COX‑2, which are needed for the production of prostaglandins. Lower prostaglandin levels reduce inflammation, pain signalling and fever, providing symptomatic relief in affected tissues.

The appropriate dose of Orudis is determined by the prescribing clinician based on the patient’s condition, severity of symptoms, age, renal and hepatic function, and any concomitant medications. The prescriber will set the exact dosage and schedule.

Ketoprofen is generally avoided in the third trimester of pregnancy because it may affect fetal ductus arteriosus closure. Use during earlier stages or while breastfeeding should only be considered if the potential benefit outweighs the risk and after consultation with a healthcare professional.

To order Orudis, 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.

Ketoprofen offers analgesic and anti‑inflammatory potency comparable to ibuprofen and diclofenac, with a relatively rapid onset of action. Its COX‑inhibition profile is similar to other non‑selective NSAIDs, but individual patient response and tolerability may differ, influencing drug choice.

Store Orudis tablets at temperatures below 25 °C in the original container, protecting them from moisture and light. Keep the product out of reach of children and do not use if the packaging is damaged.

Orudis is administered orally as a tablet. It should be swallowed whole with water, preferably with food or a glass of milk to minimise gastrointestinal irritation.

Serious risks include gastrointestinal ulceration or bleeding, renal impairment, hepatotoxicity, severe skin reactions such as Stevens‑Johnson syndrome, and anaphylaxis. Patients should be monitored for signs of these events and seek immediate medical attention if they occur.

Orudis should be avoided by individuals with known hypersensitivity to ketoprofen or other NSAIDs, those with active gastrointestinal ulceration, severe heart failure, advanced renal or hepatic disease, and pregnant women in the third trimester. Consultation with a healthcare professional is essential before starting therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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