Eusef
Generic Name
Cefoperazone Sodium
Manufacturer
Square Pharmaceuticals Ltd.
Country
Bangladesh
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Price Details
Current market pricing information
Variant | Unit Price | Strip Price |
---|---|---|
eusef 500 mg injection | ৳ 50.00 | N/A |
Description
Overview of the medicine
Eusef 500 mg Injection contains Cefoperazone, a broad-spectrum third-generation cephalosporin antibiotic. It is used to treat a wide range of bacterial infections by stopping the growth of bacteria.
Uses & Indications
Dosage
Adults
Typical dose is 2-4 grams daily, given in equally divided doses every 12 hours. For severe infections, the daily dose may be increased up to 12 grams in 2-3 divided doses. For Eusef 500 mg, this implies multiple vials per day.
Elderly
No specific dosage adjustment is generally required based on age alone, but renal and hepatic function should be assessed.
Renal_impairment
In severe renal impairment (creatinine clearance <18 mL/min), the total daily dose should not exceed 4 grams. Monitor serum concentrations in such patients.
How to Take
Eusef Injection can be administered intravenously (IV) via slow infusion over 15-30 minutes, or as an intramuscular (IM) injection. For IM administration, a suitable diluent like sterile water for injection or lidocaine solution (if permitted) should be used.
Mechanism of Action
Cefoperazone inhibits bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs), leading to bacterial cell lysis and death. It is bactericidal.
Pharmacokinetics
Onset
Rapid, typically within minutes of IV administration.
Excretion
Approximately 70-80% is excreted in the bile and up to 20-30% via the kidneys.
Half life
Approximately 2 hours in adults with normal renal and hepatic function.
Absorption
Rapidly absorbed after intramuscular (IM) or intravenous (IV) administration. Peak serum concentrations are reached shortly after IV infusion and within 1-2 hours after IM injection.
Metabolism
Minimally metabolized; primarily excreted unchanged.
Side Effects
Contraindications
- Known hypersensitivity to cefoperazone or any other cephalosporin antibiotics.
- History of severe hypersensitivity reaction to any beta-lactam antibiotic (e.g., penicillins).
Drug Interactions
Alcohol
Disulfiram-like reaction (flushing, sweating, headache, tachycardia) when consumed with alcohol due to inhibition of aldehyde dehydrogenase.
Aminoglycosides
Although generally not nephrotoxic when co-administered, renal function should be monitored, especially in patients with pre-existing renal impairment.
Anticoagulants (e.g., Warfarin)
May enhance the anticoagulant effect by interfering with vitamin K synthesis and platelet function, increasing the risk of bleeding. Monitor INR.
Loop Diuretics (e.g., Furosemide)
Can increase the risk of nephrotoxicity with certain cephalosporins, though less common with cefoperazone. Monitor renal function.
Storage
Store in a cool, dry place, below 30°C. Protect from light and moisture. Keep out of reach of children.
Overdose
Overdose symptoms may include neurological effects such as convulsions. Management involves symptomatic and supportive treatment, including maintaining airway, breathing, and circulation. Hemodialysis may be useful in removing the drug from the system, especially in patients with impaired renal function.
Pregnancy & Lactation
Pregnancy Category B. Studies in animals have shown no evidence of harm to the fetus. However, use in pregnancy should only be considered if clearly needed. Cefoperazone is excreted in small amounts in breast milk; caution should be exercised when administered to a nursing mother. Consult your doctor.
Frequently Asked Questions
Common questions about this medicine
Pack Sizes
Shelf Life
24 to 36 months from manufacturing date, depending on specific manufacturer guidelines.
Availability
Pharmacies, Hospitals, Clinics
Approval Status
Approved by DGDA
Patent Status
Generic available
WHO Essential Medicine
YesClinical Trials
Cefoperazone has undergone extensive clinical trials demonstrating its efficacy and safety profile across various bacterial infections. Post-marketing surveillance continues to monitor its use.
Lab Monitoring
- Complete Blood Count (CBC) including platelet count, especially during prolonged therapy.
- Liver function tests (AST, ALT, ALP, bilirubin).
- Renal function tests (creatinine, BUN) for patients with pre-existing renal impairment.
- Prothrombin Time (PT) / International Normalized Ratio (INR) for patients at risk of bleeding or on concomitant anticoagulants.
Doctor Notes
- Perform culture and sensitivity tests prior to initiating therapy to confirm susceptibility.
- Monitor Prothrombin Time (PT) / INR, especially in patients with impaired liver function, poor nutritional status, or those on concomitant anticoagulants.
- Educate patients about the importance of avoiding alcohol during and after treatment.
Patient Guidelines
- Complete the full course of treatment even if symptoms improve to prevent recurrence and development of antibiotic resistance.
- Report any severe or persistent side effects, especially severe diarrhea, to your doctor immediately.
- Inform your doctor about all other medications you are taking, including herbal supplements and over-the-counter drugs.
- Avoid alcohol while taking this medicine and for at least 72 hours afterward.
Missed Dose Advice
If you miss a dose, take it as soon as you remember. If it is almost time for your next dose, skip the missed dose and continue with your regular dosing schedule. Do not double the dose to catch up.
Driving Precautions
This medicine may cause dizziness in some individuals. If you experience dizziness, avoid driving or operating heavy machinery.
Lifestyle Advice
- Maintain good hydration by drinking plenty of fluids.
- Avoid activities that require mental alertness if you experience dizziness.
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Global Brand Names
International brand names for this medicine
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