Product image of Ketanov (Ketorolac Trometamol) supplied by GNH India

Ketanov

Active Ingredient:
Ketorolac Trometamol
Origin:
EU

Ketanov (Ketorolac Trometamol)

Ketorolac Trometamol, the active ingredient in Ketanov, is a nonsteroidal anti-inflammatory drug presented as a oral formulation for oral use. It is employed for short‑term management of moderate to severe pain, especially postoperative pain, in adult patients.

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

Manufacturer / TM Owner

Sun Pharmaceutical Industries Europe B.V.

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Indications & Clinical Uses

Ketanov, a nonsteroidal anti‑inflammatory analgesic, is indicated for conditions that require rapid pain control.

  • Postoperative pain: provides effective relief after surgical procedures.
  • Acute moderate‑to‑severe pain: reduces pain intensity in short‑term settings.
  • Short‑term pain management: used for brief periods when stronger analgesia is needed.

How It Works

  • Ketorolac Trometamol inhibits cyclooxygenase (COX‑1 and COX‑2) enzymes, which blocks the conversion of arachidonic acid to prostaglandins. By lowering prostaglandin synthesis, it reduces inflammation, nociceptor sensitisation and the perception of pain, delivering rapid analgesic effect after oral administration.

Side Effects

Adverse reactions may range from mild to severe and should be monitored during therapy.

Common Side Effects

  • Dyspepsia: stomach discomfort or indigestion.
  • Nausea: feeling of sickness.
  • Headache: mild to moderate head pain.
  • Dizziness: transient light‑headedness.
  • Diarrhoea: loose stools.
  • Elevated blood pressure: modest rise in systolic/diastolic values.

Serious or Rare Side Effects

  • Gastrointestinal ulceration or bleeding.
  • Renal impairment: reduced kidney function.
  • Severe hypersensitivity reactions: rash, angioedema, anaphylaxis.
  • Hepatotoxicity: abnormal liver enzymes.
  • Cardiovascular events: myocardial infarction or stroke.
  • Hematologic abnormalities: thrombocytopenia or bleeding disorders.

Precautions & Warnings

Before prescribing Ketanov, clinicians should evaluate patient‑specific risk factors and monitor for potential complications.

  • Renal function: assess baseline creatinine and avoid in severe renal impairment.
  • Gastrointestinal risk: avoid in patients with active ulcer disease or history of GI bleeding.
  • Cardiovascular disease: use cautiously in patients with coronary artery disease or uncontrolled hypertension.
  • Concomitant NSAIDs or anticoagulants: increase bleeding risk; monitor closely.
  • Pregnancy and lactation: avoid unless benefits outweigh risks; data are limited.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Ketorolac can interact with several drug classes, altering efficacy or safety.

Major Interactions (Avoid)

  • Anticoagulants (e.g., warfarin): heightened risk of serious bleeding.
  • Other NSAIDs or COX‑2 inhibitors: additive gastrointestinal toxicity.
  • Selective serotonin reuptake inhibitors (SSRIs): increased bleeding tendency.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or ARBs: may reduce renal perfusion, especially in dehydrated patients.
  • Diuretics: potential for reduced renal function.
  • Lithium: NSAIDs can raise lithium levels, risking toxicity.
  • Methotrexate: decreased clearance may lead to toxicity.

Frequently Asked Questions

Ketanov contains ketorolac trometamol, an NSAID indicated for short‑term relief of moderate to severe pain, particularly after surgery or other acute painful conditions. It is prescribed when rapid analgesia is required for a limited duration.

Ketorolac trometamol blocks cyclooxygenase‑1 and‑2 enzymes, preventing the formation of prostaglandins that mediate inflammation and pain. By reducing prostaglandin levels, it diminishes peripheral sensitisation and provides potent analgesic effects after oral dosing.

The specific dose of Ketanov is determined by the prescribing clinician based on the patient’s condition, age, renal function and other factors. Only a qualified health professional should set the dosage regimen.

Safety data for ketorolac in pregnancy and lactation are limited. It is generally avoided unless the potential benefit justifies the possible risk to the fetus or infant. Women who are pregnant, planning pregnancy, or breastfeeding should discuss alternatives with their healthcare provider.

To order Ketanov, 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.

Ketanov (ketorolac) is a potent NSAID with stronger analgesic activity than many over‑the‑counter agents such as ibuprofen or naproxen, making it suitable for short‑term, high‑intensity pain. However, its risk profile for gastrointestinal and renal adverse events is also higher, so it is reserved for brief use under medical supervision.

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

Ketanov is taken orally, usually with a full glass of water. It can be taken with or without food, but patients with a history of stomach upset may benefit from taking it with meals to reduce gastrointestinal irritation.

Serious risks include gastrointestinal bleeding or ulceration, severe renal impairment, cardiovascular events such as myocardial infarction or stroke, and rare but life‑threatening hypersensitivity reactions. Patients should be monitored closely for signs of these complications.

Ketanov is contraindicated in patients with known hypersensitivity to ketorolac or other NSAIDs, active peptic ulcer disease, severe renal or hepatic impairment, and those who have had recent coronary artery bypass graft surgery. It should also be avoided in pregnancy unless absolutely necessary.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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