Keteks
Generic Name
Keteks 30 mg Injection
Manufacturer
Square Pharmaceuticals Ltd. (example for Bangladesh)
Country
Bangladesh
Loading images...
Price Details
Current market pricing information
| Variant | Unit Price | Strip Price |
|---|---|---|
| keteks 30 mg injection | ৳ 55.00 | N/A |
Description
Overview of the medicine
Keteks 30 mg Injection contains Ketorolac Tromethamine, a non-steroidal anti-inflammatory drug (NSAID) used for the short-term management of moderate to severe acute pain. It is often administered post-operatively or for other acute painful conditions where oral administration is not feasible.
Uses & Indications
Dosage
Adults
Initial dose: 30 mg IM or IV once. Subsequent doses: 30 mg every 6 hours as needed. Maximum daily dose: 120 mg. Duration of treatment not to exceed 5 days.
Elderly
For patients ≥ 65 years, a reduced dosage may be necessary, typically 15 mg every 6 hours. Maximum daily dose: 60 mg. Max 5 days.
Renal_impairment
Contraindicated in advanced renal impairment. For mild to moderate impairment, dosage reduction to 15 mg every 6 hours (max 60 mg/day) may be required. Careful monitoring is essential.
How to Take
For intramuscular (IM) or intravenous (IV) administration. IM injections should be given slowly and deeply into a large muscle. IV bolus injections should be administered over no less than 15 seconds. Ensure aseptic technique.
Mechanism of Action
Ketorolac Tromethamine primarily acts by inhibiting prostaglandin synthesis through the inhibition of cyclooxygenase (COX-1 and COX-2) enzymes. This results in reduced inflammation, pain, and fever.
Pharmacokinetics
Onset
Analgesic onset typically within 30 minutes.
Excretion
Mainly renal; approximately 91% of a dose is excreted in urine (60% as parent drug, 40% as metabolites) and 6% in feces.
Half life
Mean terminal plasma half-life is approximately 5-6 hours.
Absorption
Rapid and complete absorption after intramuscular (IM) administration. Peak plasma concentrations achieved in approximately 30-60 minutes.
Metabolism
Primarily hepatic, largely via hydroxylation and conjugation. Minor metabolites are inactive.
Side Effects
Contraindications
- •Active peptic ulcer disease, recent gastrointestinal bleeding or perforation, or history of these conditions.
- •Advanced renal impairment or risk of renal failure due to dehydration.
- •Hypersensitivity to ketorolac, aspirin, or other NSAIDs (e.g., aspirin-induced asthma, urticaria, or allergic-type reactions).
- •Concomitant use with other NSAIDs, aspirin, anticoagulants (e.g., warfarin, heparin), probenecid, or pentoxifylline.
- •Patients with cerebrovascular bleeding or other bleeding disorders.
- •During labor and delivery (due to effect on fetal circulation and inhibition of uterine contractions).
- •As prophylactic analgesic before major surgery with high risk of hemorrhage.
- •Neuraxial (epidural or intrathecal) administration.
Drug Interactions
Lithium
Increased plasma lithium levels, potentially leading to toxicity.
Probenecid
Increased plasma concentration and half-life of Ketorolac.
Methotrexate
Increased plasma methotrexate levels, potentially leading to toxicity.
Pentoxifylline
Increased risk of bleeding.
ACE Inhibitors/ARBs
Increased risk of renal impairment, especially in elderly or dehydrated patients.
Other NSAIDs or Aspirin
Increased risk of GI adverse effects and bleeding.
Diuretics (e.g., Furosemide, Thiazides)
Reduced natriuretic effect and potential for renal toxicity.
Anticoagulants (e.g., Warfarin, Heparin)
Increased risk of bleeding.
Storage
Store at controlled room temperature (20-25°C or 68-77°F). Protect from light. Do not freeze.
Overdose
Symptoms of overdose may include drowsiness, nausea, vomiting, epigastric pain, GI bleeding, lethargy, and anaphylactoid reactions. Management is primarily supportive and symptomatic. Gastric decontamination (e.g., activated charcoal) may be considered if taken orally, but for injection, supportive care (e.g., maintaining airway, monitoring vital signs, managing fluid and electrolyte balance) is crucial. Hemodialysis is not likely to remove significant amounts.
Pregnancy & Lactation
Pregnancy Category C (first and second trimester), Category D (third trimester). Contraindicated in the third trimester of pregnancy due to potential for premature closure of the fetal ductus arteriosus. Contraindicated during labor and delivery. Not recommended during breastfeeding as ketorolac is excreted in human milk and could have adverse effects on the nursing infant.
Frequently Asked Questions
Common questions about this medicine
Pack Sizes
Shelf Life
Refer to manufacturer's packaging, typically 2-3 years from manufacturing date when stored correctly.
Availability
Hospitals, Clinics, Pharmacies (with prescription)
Approval Status
Approved by regulatory authorities (e.g., DGDA, FDA)
Patent Status
Generic versions available, patent expired for Ketorolac
Alternative Medicines in Bangladesh
Similar medicines available in the market
Global Brand Names
International brand names for this medicine
More Medicines
Explore other medicines you might be interested in


