Product image of Ketorolac S.A.L.F. (Ketorolac Trometamol) supplied by GNH India

Ketorolac S.A.L.F.

Active Ingredient:
Ketorolac Trometamol
Origin:
EU

Ketorolac S.A.L.F. (Ketorolac Trometamol)

Ketorolac Trometamol, the active ingredient in Ketorolac S.A.L.F., is a nonsteroidal anti‑inflammatory drug presented as an injectable solution for intramuscular and intravenous use. It provides short‑term management of moderate to severe pain, including post‑operative pain, in adult patients.

GNH India supplies Ketorolac S.A.L.F. as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

S.A.L.F. Spa Laboratorio Farmacologico

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Indications & Clinical Uses

Ketorolac Trometamol is an NSAID used for acute pain management in the postoperative setting and other short‑term severe pain conditions.

  • Post‑operative pain: provides rapid analgesia after surgical procedures.
  • Acute musculoskeletal pain: reduces pain following injury or trauma.
  • Short‑term severe pain: offers effective non‑opioid relief for moderate to severe pain when brief therapy is appropriate.

How It Works

  • Ketorolac Trometamol inhibits cyclooxygenase (COX‑1 and COX‑2) enzymes, blocking the conversion of arachidonic acid to prostaglandins. The reduction in prostaglandin synthesis diminishes peripheral sensitisation and inflammatory mediators, leading to decreased pain perception and inflammation at the site of injury.

Side Effects

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

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Headache: transient discomfort.
  • Dizziness: occasional light‑headedness.
  • Injection site pain: local irritation.
  • Gastrointestinal discomfort: dyspepsia or mild abdominal pain.
  • Vomiting: occasional episodes.

Serious or Rare Side Effects

  • Gastrointestinal bleeding: potentially life‑threatening hemorrhage.
  • Renal impairment: reduced kidney function or acute failure.
  • Severe allergic reactions: anaphylaxis, angioedema.
  • Cardiovascular events: myocardial infarction or stroke.
  • Hematologic abnormalities: thrombocytopenia or bleeding disorders.
  • Skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.

Precautions & Warnings

Ketorolac should be used with caution and under professional supervision.

  • Renal function assessment: evaluate kidney status before initiation.
  • Hypersensitivity screening: avoid in patients with known NSAID allergy.
  • Dose minimisation: use the lowest effective dose for the shortest duration.
  • Bleeding risk monitoring: watch for signs of gastrointestinal or intracranial bleeding.
  • Cardiovascular caution: be careful in patients with existing heart disease.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Ketorolac can interact with several medication classes, requiring attention to avoid adverse outcomes.

Major Interactions (Avoid)

  • Anticoagulants (e.g., warfarin): increased risk of bleeding.
  • Other NSAIDs: additive gastrointestinal toxicity.
  • ACE inhibitors: potential reduction in renal function.
  • Lithium: heightened lithium levels and toxicity.
  • Methotrexate: reduced clearance leading to toxicity.

Moderate Interactions (Monitor Closely)

  • Diuretics: possible renal function changes.
  • Corticosteroids: enhanced risk of gastrointestinal ulceration.
  • SSRIs: modest increase in bleeding tendency.
  • Antihypertensives: may blunt blood pressure control.
  • Beta‑blockers: potential for reduced analgesic effect.

Frequently Asked Questions

Ketorolac S.A.L.F. is an injectable non‑steroidal anti‑inflammatory drug indicated for short‑term management of moderate to severe pain, such as post‑operative pain or acute musculoskeletal pain, when rapid analgesia is required.

Ketorolac Trometamol blocks cyclooxygenase enzymes (COX‑1 and COX‑2), which reduces the formation of prostaglandins. Lower prostaglandin levels decrease inflammation and pain signalling, providing effective analgesia.

The specific dose and administration schedule are determined by the prescribing clinician based on the patient’s condition, weight, renal function, and treatment duration. Ketorolac is typically limited to short‑term use.

Safety data for Ketorolac in pregnancy and lactation are limited. It is generally avoided in the third trimester and used only if the potential benefit justifies the risk. Breastfeeding mothers should consult their healthcare provider.

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 import documentation.

Ketorolac is distinguished by its potent analgesic effect, often comparable to opioid analgesics for short‑term use, whereas many NSAIDs provide milder pain relief. However, its risk profile for gastrointestinal and renal adverse events is higher, so it is reserved for brief treatment periods.

Ketorolac S.A.L.F. should be stored at 2‑8 °C, protected from light, and kept in the original packaging. Do not freeze or shake the vial, and discard any solution that appears discoloured or particulate.

The product is supplied as an injectable solution for intramuscular or intravenous administration. It must be administered by a qualified healthcare professional using aseptic technique, following the dosage prescribed by the clinician.

Serious risks include gastrointestinal bleeding, renal failure, severe allergic reactions such as anaphylaxis, and cardiovascular events like myocardial infarction or stroke. Patients should be monitored closely for signs of these complications.

Ketorolac is contraindicated in patients with known hypersensitivity to ketorolac or other NSAIDs, active gastrointestinal ulceration, severe renal impairment, and in the third trimester of pregnancy. It should also be avoided in patients receiving certain anticoagulants without careful risk assessment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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