Product image of Ketoprofene Aguettant (Ketoprofen) supplied by GNH India

Ketoprofene Aguettant

Active Ingredient:
Ketoprofen
Origin:
EU

Ketoprofene Aguettant (Ketoprofen)

Ketoprofen, the active ingredient in Ketoprofene Aguettant, is a nonsteroidal anti-inflammatory drug presented as an intravenous solution for intravenous use. It treats pain, inflammation and postoperative discomfort in adult patients and is indicated for management of acute pain, inflammatory conditions such as rheumatoid arthritis, and postoperative pain following surgical procedures.

GNH India supplies Ketoprofene Aguettant as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, with distribution channels that meet European Union regulatory standards and ensure product integrity throughout the supply chain.

Manufacturer / TM Owner

Laboratoire Aguettant

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Indications & Clinical Uses

Ketoprofen is an NSAID that reduces inflammation and pain by inhibiting cyclooxygenase enzymes.

  • Postoperative pain: provides analgesia and attenuates inflammatory response after surgical procedures.
  • Rheumatoid arthritis: helps control joint inflammation and pain in chronic inflammatory disease.
  • Acute musculoskeletal pain: relieves pain and swelling associated with sprains, strains or trauma.
  • Inflammatory conditions: reduces swelling and discomfort in various acute inflammatory states.

How It Works

  • Ketoprofen exerts its effect by non‑selectively inhibiting cyclooxygenase‑1 (COX‑1) and cyclooxygenase‑2 (COX‑2) enzymes, which blocks the conversion of arachidonic acid to prostaglandins. The resulting decrease in prostaglandin synthesis diminishes inflammation, pain signaling, and fever responses at the site of tissue injury.

Side Effects

Ketoprofene Aguettant may cause a range of adverse reactions, which are grouped by frequency and severity.

Common Side Effects

  • Nausea: mild to moderate stomach upset experienced after infusion.
  • Dyspepsia: indigestion or heartburn that may persist for several hours.
  • Headache: transient cranial discomfort often resolving without intervention.
  • Injection site pain: local discomfort or mild irritation at the infusion site.

Serious or Rare Side Effects

  • Gastrointestinal bleeding: potentially life‑threatening hemorrhage from the stomach or intestines.
  • Renal impairment: reduced kidney function that can progress to failure if untreated.
  • Severe allergic reaction: anaphylaxis, skin rash or angioedema requiring immediate medical care.
  • Hepatic dysfunction: elevated liver enzymes or hepatitis presenting with jaundice or fatigue.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient‑specific risk factors and follow safety guidelines.

  • Assess renal function: evaluate kidney status prior to and during treatment.
  • Monitor gastrointestinal risk: consider ulcer history and use gastro‑protective agents when appropriate.
  • Evaluate cardiovascular history: avoid in patients with uncontrolled hypertension or recent cardiac events.
  • Use lowest effective dose: limit duration to reduce the likelihood of adverse events.
  • Avoid in known hypersensitivity: discontinue immediately if allergic signs appear.
  • Store at room temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Ketoprofene Aguettant can alter the activity of several concomitant medicines; interactions are classified by clinical significance.

Major Interactions (Avoid)

  • Anticoagulants (e.g., warfarin): increased risk of serious bleeding.
  • Other NSAIDs or aspirin: additive gastrointestinal toxicity and ulcer risk.
  • Corticosteroids: heightened potential for ulceration and bleeding.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or ARBs: may reduce renal function when combined.
  • Diuretics: potential for decreased kidney perfusion and electrolyte imbalance.
  • Methotrexate: reduced clearance can lead to toxicity.

Frequently Asked Questions

Ketoprofene Aguettant is an intravenous formulation of ketoprofen used to relieve moderate to severe pain, reduce inflammation, and manage postoperative discomfort. It is also employed in the treatment of inflammatory conditions such as rheumatoid arthritis when rapid systemic effect is required.

Ketoprofen works by non‑selectively blocking the cyclooxygenase‑1 and cyclooxygenase‑2 enzymes, which are essential for converting arachidonic acid into prostaglandins. By lowering prostaglandin levels, it diminishes inflammation, pain signaling, and fever responses at the site of injury.

The specific dose and infusion rate of Ketoprofene Aguettant are determined by the prescribing clinician based on the patient’s condition, weight, renal and hepatic function, and response to therapy. No fixed dosing regimen is provided here; the prescriber tailors the regimen to each individual.

Safety data for ketoprofen in pregnancy and lactation are limited. It should only be used when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and only under close medical supervision. Breastfeeding mothers should discuss alternatives with their healthcare provider.

To place an order, 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 needed) and required import documentation.

Ketoprofene Aguettant, delivered intravenously, offers rapid systemic exposure compared with oral ibuprofen, which may be advantageous in acute postoperative settings. Both share a similar COX‑inhibition profile, but ketoprofen generally provides a longer duration of analgesia, while ibuprofen is available in oral and topical forms for outpatient use.

Ketoprofene Aguettant should be stored at room temperature, below 25 °C, in its original packaging. Protect the solution from moisture and direct sunlight. Do not freeze. Inspect the container for any particulate matter or discoloration before use, and follow aseptic techniques during preparation.

The product is supplied as a sterile intravenous solution. It is administered by a qualified healthcare professional via slow IV infusion, typically over 15–30 minutes, according to the prescriber’s instructions. Monitoring of vital signs and infusion site is recommended during administration.

Serious risks include gastrointestinal bleeding, which can be life‑threatening; acute renal impairment or failure, especially in patients with pre‑existing kidney disease; severe allergic reactions such as anaphylaxis; and hepatic dysfunction. Patients should be monitored closely for signs of these events, and therapy should be stopped if they occur.

Ketoprofene Aguettant is contraindicated in individuals with known hypersensitivity to ketoprofen or other NSAIDs, active peptic ulcer disease, severe uncontrolled hypertension, significant renal or hepatic impairment, and in patients who have experienced previous serious cardiovascular events related to NSAID use.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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