Product image of Ketorolaco Trometamol Qualigen (Ketorolac Trometamol) supplied by GNH India

Ketorolaco Trometamol Qualigen

Active Ingredient:
Ketorolac Trometamol
Origin:
EU

Ketorolaco Trometamol Qualigen (Ketorolac Trometamol)

Ketorolac Trometamol, the active ingredient in Ketorolaco Trometamol Qualigen, is a nonsteroidal anti-inflammatory drug (NSAID) presented as an oral formulation for oral use. It is indicated for moderate to severe acute pain, post‑operative pain, and short‑term pain management in adult patients.

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

Manufacturer / TM Owner

Neuraxpharm Spain, S.L.U.

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Indications & Clinical Uses

Ketorolac Trometamol is an NSAID used to control pain through inhibition of prostaglandin synthesis.

  • Moderate to severe acute pain: provides rapid analgesia for intense pain episodes.
  • Post‑operative pain: reduces pain and inflammation after surgical procedures.
  • Short‑term pain management: offers effective relief for brief periods of pain when other agents are insufficient.

How It Works

  • Ketorolac Trometamol exerts its effect by non‑selectively inhibiting cyclooxygenase‑1 (COX‑1) and cyclooxygenase‑2 (COX‑2) enzymes. This blockade decreases the conversion of arachidonic acid to prostaglandins, leading to reduced inflammation, lowered peripheral sensitization, and diminished perception of pain at the site of injury.

Side Effects

Ketorolac Trometamol may cause a range of adverse reactions, from mild to severe.

Common Side Effects

  • Gastrointestinal discomfort or dyspepsia.
  • Nausea or vomiting.
  • Headache.
  • Dizziness or vertigo.
  • Transient renal function changes.
  • Mild skin rash.

Serious or Rare Side Effects

  • Gastrointestinal bleeding or ulcer perforation.
  • Severe renal impairment or failure.
  • Cardiovascular thrombotic events (e.g., myocardial infarction, stroke).
  • Anaphylactic or severe hypersensitivity reactions.
  • Hepatotoxicity with elevated liver enzymes.

Precautions & Warnings

Before prescribing Ketorolac Trometamol, clinicians should evaluate patient‑specific risk factors and monitor for adverse events.

  • Assess renal function: avoid in patients with severe renal impairment.
  • Evaluate gastrointestinal risk: use cautiously in those with a history of ulcers or bleeding.
  • Avoid in active ulcer disease or gastrointestinal perforation.
  • Use the lowest effective dose for the shortest duration needed.
  • Do not combine with other NSAIDs, anticoagulants, or drugs that increase bleeding risk.
  • Pregnancy and lactation: safety not established; avoid unless clearly needed.
  • Store at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

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

Major Interactions (Avoid)

  • Anticoagulants (e.g., warfarin): increased bleeding risk.
  • Other NSAIDs or aspirin: additive gastrointestinal toxicity.
  • ACE inhibitors or ARBs: heightened risk of renal impairment.
  • Lithium: elevated lithium levels leading to toxicity.
  • Methotrexate: reduced clearance and possible toxicity.

Moderate Interactions (Monitor Closely)

  • Selective serotonin reuptake inhibitors (SSRIs): modestly increased bleeding risk.
  • Diuretics: potential for reduced renal perfusion.
  • Corticosteroids: enhanced gastrointestinal ulcer risk.
  • Antihypertensives: possible attenuation of blood pressure control.
  • Oral hypoglycemics: may affect glucose control.

Frequently Asked Questions

Ketorolaco Trometamol Qualigen is an oral NSAID indicated for the treatment of moderate to severe acute pain, post‑operative pain, and short‑term pain management in adult patients. It provides rapid analgesia by reducing inflammation and pain signaling.

Ketorolac trometamol works by non‑selectively inhibiting the cyclooxygenase‑1 and cyclooxygenase‑2 enzymes, which blocks the synthesis of prostaglandins. Lower prostaglandin levels lead to decreased inflammation, reduced peripheral sensitization, and diminished perception of pain.

The dosage of ketorolac trometamol is determined by the prescribing clinician based on the severity of pain, patient characteristics, and treatment duration. The prescriber sets the appropriate dose and regimen according to clinical guidelines.

Safety of ketorolac trometamol in pregnancy and lactation has not been established. It should be avoided unless the potential benefit justifies the potential risk to the fetus or infant, and only under close medical supervision.

To order, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India supplies hospitals, pharmacies, and procurement teams worldwide, and will request trade or institutional credentials before providing pricing, availability, shipping details, and necessary import documentation.

Ketorolac is a potent NSAID with strong analgesic properties, often considered more effective for short‑term severe pain than many other NSAIDs. However, its risk profile for gastrointestinal and renal adverse events may be higher, so it is typically used for brief periods under careful monitoring.

Ketorolaco Trometamol Qualigen should be stored at ambient temperature, below 25 °C, in its original packaging. Protect the product from moisture, excessive heat, and direct sunlight to maintain its stability and potency.

The medication is taken orally, usually with a full glass of water. It may be taken with or without food, but patients should follow the prescriber’s instructions regarding timing and any specific administration guidelines.

Serious risks include gastrointestinal bleeding or ulcer perforation, severe renal impairment, cardiovascular thrombotic events such as myocardial infarction or stroke, and rare but severe hypersensitivity reactions like anaphylaxis. Prompt medical attention is required if any of these occur.

Ketorolac should not be used by patients with active gastrointestinal ulcer disease, severe renal impairment, known hypersensitivity to ketorolac or other NSAIDs, or those who are at high risk for cardiovascular events. It is also contraindicated in patients receiving other NSAIDs or anticoagulants without careful medical oversight.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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