METRONIDAZOLE (metronidazole) by Molecular Devices is mechanism of action metronidazole, a nitroimidazole, exerts antibacterial effects in an anaerobic environment against most obligate anaerobes. First approved in 1983.
Drug data last refreshed 5d ago
Metronidazole is a nitroimidazole antibiotic approved in 1983 that treats anaerobic bacterial infections, protozoal infections, and inflammatory conditions across 18+ indications including bacterial vaginosis, intra-abdominal infections, C. difficile-associated diarrhea, and rosacea. The drug works by entering anaerobic bacteria, being reduced intracellularly, and forming free radicals that degrade bacterial DNA, leading to cell death. It is available as an oral tablet and represents a foundational generic antibiotic with nearly 40 years of clinical use.
Minimal Part D utilization and approaching loss of exclusivity signal limited growth opportunity; brand team likely small or consolidated with generic portfolio.
Mechanism of Action Metronidazole, a nitroimidazole, exerts antibacterial effects in an anaerobic environment against most obligate anaerobes. Once metronidazole enters the organism by passive diffusion and is activated in the cytoplasm of susceptible anaerobic bacteria, it is reduced; this process…
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Chlorhexidine and/or Metronidazole Plus FB301 Pre-treatment Trial
A Single-center, Open-label, Study Evaluating Safety and Pharmacokinetics of Single Doses of Zidebactam-Cefepime and Metronidazole Alone or in Combination.
Effectivity and Safety of Metronidazole 1% Cream in Rosacea Therapy
Personalized AZithromycin/metronidAZole Therapy in Pediatric Crohn's Disease (CD)
Ceftolozane/Tazobactam (MK-7625A) Plus Metronidazole Versus Meropenem for Participants With Complicated Intra-abdominal Infection (MK-7625A-015)
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The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.
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