Ciprocin
Generic Name
Ciprofloxacin
Manufacturer
Square Pharmaceuticals Ltd.
Country
Bangladesh
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Price Details
Current market pricing information
Variant | Unit Price | Strip Price |
---|---|---|
ciprocin 200 mg injection | ৳ 146.00 | N/A |
Description
Overview of the medicine
Ciprofloxacin is a broad-spectrum fluoroquinolone antibiotic used to treat various bacterial infections, administered intravenously for systemic effect.
Uses & Indications
Dosage
Adults
200-400 mg every 8-12 hours by slow intravenous infusion over 30-60 minutes, depending on the type and severity of infection. Doses may be increased in severe cases.
Elderly
Dosage adjustment may be needed based on renal function.
Renal_impairment
Dose reduction is required based on creatinine clearance (e.g., CrCl 30-60 mL/min: max 400 mg every 12 hours; CrCl <30 mL/min: max 400 mg every 18-24 hours).
How to Take
Administer by slow intravenous infusion over 30-60 minutes into a large vein. Do not administer intramuscularly or subcutaneously. Ensure adequate hydration.
Mechanism of Action
Inhibits bacterial DNA gyrase and topoisomerase IV, enzymes essential for bacterial DNA replication, transcription, repair, and recombination, leading to bacterial cell death.
Pharmacokinetics
Onset
Rapid (within minutes after IV administration).
Excretion
Primarily via renal excretion (both glomerular filtration and tubular secretion), with some non-renal clearance.
Half life
3 to 5 hours (can be prolonged in renal impairment).
Absorption
Rapid and complete systemic absorption (100% bioavailability) after intravenous administration. Peak plasma concentrations are achieved at the end of infusion.
Metabolism
Partially metabolized in the liver to less active metabolites.
Side Effects
Contraindications
- Hypersensitivity to ciprofloxacin or other quinolones.
- Concomitant administration with tizanidine.
- Children and adolescents (except for specific severe infections where benefits outweigh risks).
Drug Interactions
Warfarin
Enhanced anticoagulant effects (monitor INR/PT).
Tizanidine
Increased tizanidine plasma concentrations, leading to hypotension and somnolence (contraindicated).
Cyclosporine
Increased serum creatinine and potential nephrotoxicity.
Methotrexate
Increased methotrexate plasma levels and potential toxicity.
Theophylline
Increased theophylline levels and toxicity (monitor levels).
Storage
Store below 30°C. Protect from light. Do not freeze.
Overdose
Symptoms may include renal toxicity, reversible renal impairment, and central nervous system effects (e.g., convulsions, tremors, confusion). Management is supportive and symptomatic; maintain hydration. Hemodialysis removes only small amounts of ciprofloxacin.
Pregnancy & Lactation
Pregnancy: Category C. Use only if potential benefit justifies the potential risk to the fetus. Lactation: Excreted into breast milk. Discontinue nursing or the drug.
Side Effects
Contraindications
- Hypersensitivity to ciprofloxacin or other quinolones.
- Concomitant administration with tizanidine.
- Children and adolescents (except for specific severe infections where benefits outweigh risks).
Drug Interactions
Warfarin
Enhanced anticoagulant effects (monitor INR/PT).
Tizanidine
Increased tizanidine plasma concentrations, leading to hypotension and somnolence (contraindicated).
Cyclosporine
Increased serum creatinine and potential nephrotoxicity.
Methotrexate
Increased methotrexate plasma levels and potential toxicity.
Theophylline
Increased theophylline levels and toxicity (monitor levels).
Storage
Store below 30°C. Protect from light. Do not freeze.
Overdose
Symptoms may include renal toxicity, reversible renal impairment, and central nervous system effects (e.g., convulsions, tremors, confusion). Management is supportive and symptomatic; maintain hydration. Hemodialysis removes only small amounts of ciprofloxacin.
Pregnancy & Lactation
Pregnancy: Category C. Use only if potential benefit justifies the potential risk to the fetus. Lactation: Excreted into breast milk. Discontinue nursing or the drug.
Frequently Asked Questions
Common questions about this medicine
Pack Sizes
Shelf Life
24 months from manufacturing date (typical for IV solutions)
Availability
Hospitals, Clinics, Pharmacies
Approval Status
Approved by regulatory authorities (e.g., DGDA, FDA)
Patent Status
Off-patent
WHO Essential Medicine
YesClinical Trials
Initial clinical trials established efficacy against various bacterial infections. Ongoing post-marketing surveillance continues to monitor for safety and rare adverse events.
Lab Monitoring
- Renal function tests (creatinine, BUN)
- Liver function tests (ALT, AST)
- Complete blood count (CBC)
- Electrolytes (especially potassium in patients with risk factors for QT prolongation)
Doctor Notes
- Counsel patients on the black box warnings, particularly the risk of tendinopathy and neuropathy, and to seek immediate medical attention if symptoms occur.
- Monitor renal function in elderly and renally impaired patients and adjust dosage accordingly.
- Ensure adequate hydration to minimize the risk of crystalluria.
Patient Guidelines
- Complete the full course of treatment as prescribed, even if symptoms improve, to prevent relapse and antibiotic resistance.
- Report any tendon pain, numbness, tingling, or unusual muscle weakness immediately to your doctor.
- Avoid excessive sun exposure due to the risk of photosensitivity.
- Stay well-hydrated to help prevent crystalluria.
Missed Dose Advice
If a dose is missed, administer it as soon as remembered, unless it is almost time for the next dose. Do not double the dose.
Driving Precautions
May cause dizziness or lightheadedness, impairing ability to drive or operate machinery. Patients should be cautious until they know how the drug affects them.
Lifestyle Advice
- Maintain good hygiene to prevent recurrence of infections.
- Follow a balanced diet and engage in regular, moderate exercise (if appropriate for the condition).
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