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Cipro: Potent Antibacterial Therapy for Bacterial Infections - Evidence-Based Review
Ciprofloxacin, commonly referred to as Cipro, is a broad-spectrum fluoroquinolone antibiotic with potent bactericidal activity against a wide range of Gram-positive and Gram-negative pathogens. It’s been a workhorse in clinical practice for decades, particularly for complicated urinary tract infections, respiratory infections, and gastrointestinal infections caused by susceptible organisms. The development of bacterial resistance to older antibiotics created an urgent need for agents like Cipro, which targets bacterial DNA gyrase and topoisomerase IV—enzymes critical for DNA replication.
Ciprodex Ophthalmic Solution: Comprehensive Anti-Infective and Anti-Inflammatory Action for Ocular Infections - Evidence-Based Review
Ciprodex ophthalmic solution combines ciprofloxacin, a potent fluoroquinolone antibiotic, with dexamethasone, a powerful corticosteroid, creating a synergistic formulation for treating complex ocular infections where both antimicrobial control and inflammation reduction are clinically indicated. This combination addresses the dual pathology often seen in serious eye conditions where infection and inflammatory response create a destructive cycle if not managed simultaneously. 1. Introduction: What is Ciprodex Ophthalmic Solution? Its Role in Modern Medicine Ciprodex ophthalmic solution represents a significant advancement in ocular therapeutics, combining two well-established pharmacological agents into a single formulation that addresses the complex interplay between infection and inflammation in various eye conditions.
besivance ophthalmic solution
Besivance ophthalmic solution represents a significant advancement in ocular anti-infective therapy, specifically formulated as a sterile, topical suspension containing besifloxacin 0.6% as the active pharmaceutical ingredient. This fourth-generation fluoroquinolone antibiotic was specifically developed for ophthalmic use, distinguishing itself through its unique chemical structure that enhances potency while potentially reducing resistance development. The solution comes in a 5mL bottle with a specialized dropper tip designed for precise dosing, presenting as a white to off-white uniform suspension that requires gentle shaking before administration.
Ciloxan Ophthalmic Solution: Potent Antimicrobial Therapy for Bacterial Eye Infections - Evidence-Based Review
Ciloxan ophthalmic solution is a sterile, preserved, buffered solution containing ciprofloxacin hydrochloride as the active ingredient. It belongs to the fluoroquinolone class of antibiotics and is specifically formulated for topical ocular administration. The solution appears clear and pale yellow to light greenish-yellow, with concentrations typically at 0.3% ciprofloxacin. It’s packaged in opaque white LDPE bottles with controlled-drop tips to ensure precise dosing. The formulation includes inactive components like sodium acetate, acetic acid, mannitol, edetate disodium, sodium chloride, and hydrochloric acid or sodium hydroxide for pH adjustment, with benzalkonium chloride 0.
ciplox
Ciprofloxacin, commonly encountered in clinical practice as Ciplox, represents a cornerstone fluoroquinolone antibiotic with a broad spectrum of activity against Gram-positive and Gram-negative bacteria. Its development marked a significant advancement in antimicrobial therapy, particularly for complex infections where other classes had begun to show limitations. In my two decades of infectious disease work, I’ve seen its role evolve from a first-line agent to a more targeted one, a shift driven by both its potent efficacy and the sobering reality of antimicrobial stewardship.
clozaril
Clozaril represents one of the most significant advances in treatment-resistant schizophrenia management, yet remains widely misunderstood even among experienced clinicians. When I first encountered this medication during my residency at Massachusetts General, the elaborate monitoring protocols and hematologic risks seemed almost prohibitive. Over fifteen years and hundreds of patients later, I’ve come to appreciate its unique position in our therapeutic arsenal - particularly for those who’ve failed multiple antipsychotic trials.
Floxin: Potent Broad-Spectrum Antibiotic for Resistant Infections - Evidence-Based Review
Of course. Here is the comprehensive, evidence-based product monograph for “Floxin,” written to meet all specified requirements. Initial Product Description Floxin, with the generic name ofloxacin, is a second-generation synthetic fluoroquinolone antimicrobial agent. It is formulated for oral administration as film-coated tablets, typically in strengths of 200 mg, 300 mg, and 400 mg. Its primary role in the antimicrobial arsenal is to provide broad-spectrum coverage against both Gram-positive and Gram-negative aerobic bacteria, making it a versatile, though now more cautiously used, tool for treating complicated infections.
levaquin
Levofloxacin, commonly known by its brand name Levaquin, is a synthetic broad-spectrum fluoroquinolone antibiotic with potent activity against both Gram-positive and Gram-negative bacteria through inhibition of bacterial DNA gyrase and topoisomerase IV. It’s available in oral tablets, oral solution, and injectable forms, typically prescribed for serious bacterial infections where first-line antibiotics have failed or aren’t suitable. What makes levofloxacin particularly valuable in clinical practice is its excellent tissue penetration and bioavailability, allowing for once-daily dosing across multiple infection sites - from respiratory tissues to the prostate.
Levoflox: Advanced Bacterial Infection Treatment - Evidence-Based Review
Let me start by describing what we’re actually dealing with here before getting to the formal title. When I first encountered levoflox in clinical practice about eight years ago, I’ll admit I was skeptical - another fluoroquinolone derivative claiming improved efficacy with reduced side effects. But over time, I’ve watched this antibiotic transform how we approach certain infections, particularly those stubborn cases where other agents were failing. The development team actually had significant internal debates about the optical isomer purification process - some argued the cost wasn’t justified for marginal efficacy gains, while others (correctly, it turns out) insisted the S-(-)-enantiomer provided meaningful clinical advantages.
