Ciprofloxacin
Cipro
Overview
Ciprofloxacin is a broad-spectrum fluoroquinolone antibiotic used to treat a variety of bacterial infections including urinary tract, respiratory, gastrointestinal, and skin infections.
Indications
- Urinary tract infections
- Respiratory tract infections
- Gastrointestinal infections
- Skin and soft tissue infections
- Anthrax post-exposure prophylaxis
Contraindications
- Hypersensitivity to fluoroquinolones
- Concurrent tizanidine use
Classification
Mechanism of Action
Inhibits bacterial DNA gyrase (topoisomerase II) and topoisomerase IV, blocking DNA replication, transcription, and repair and producing bactericidal activity.
Pharmacodynamics
Exhibits concentration-dependent bactericidal killing with a post-antibiotic effect against many gram-negative and some gram-positive organisms.
Pharmacokinetics
- Absorption
- Well absorbed orally with bioavailability around 70%.
- Distribution
- Widely distributed into tissues and body fluids; moderate protein binding.
- Metabolism
- Partially metabolized in the liver to less active metabolites.
- Excretion
- Excreted mainly in urine as unchanged drug and metabolites.
- Half-life
- Approximately 4 hours
- Bioavailability
- Approximately 70%
- Protein Binding
- Approximately 20-40%
Dosage
Typical dosage: 250-750 mg every 12 hours depending on infection
Available Forms
- Tablet
- Extended-release tablet
- Oral suspension
- Injection
- Ophthalmic solution
Side Effects
Common
- Nausea
- Diarrhea
- Headache
- Dizziness
Serious
- Tendon rupture
- Peripheral neuropathy
- QT prolongation
- Clostridioides difficile colitis
Rare
- Aortic aneurysm or dissection
- Seizures
Drug Interactions
Ciprofloxacin markedly inhibits tizanidine metabolism, causing severe hypotension and sedation; the combination is contraindicated.
May potentiate warfarin, increasing INR and bleeding risk.
Warnings
Fluoroquinolones, including ciprofloxacin, are associated with disabling and potentially irreversible serious adverse reactions including tendinitis and tendon rupture, peripheral neuropathy, and central nervous system effects, and can exacerbate muscle weakness in myasthenia gravis. Reserve use for infections with no alternative treatment options.
Pregnancy
Category C
Toxicity
Overdose may cause renal toxicity and crystalluria.
Overdose
Provide supportive care and adequate hydration; monitor renal function. Only a small amount is removed by hemodialysis.
References
Looking for patient-friendly information? Visit RemedyDoor for easy-to-read guides about this medication.