Metronidazole
Детермінований перегляд YAML-сутності з джерельної бази. Клінічний авторитет лишається за вказаними source ID та статусом клінічного sign-off.
| ID | DRUG-METRONIDAZOLE |
|---|---|
| Тип | Препарат |
| Синоніми | FlagylMetrogylTrichopolumМетронідазол |
| Статус | переглянуто 2026-04-27 | очікує клінічного підпису |
| Хвороби | Не вказано |
| Джерела | SRC-NCCN-BCELL-2025 SRC-NCCN-MM-2025 |
Дані про препарат
| Клас | Nitroimidazole antibiotic / antiprotozoal (anaerobic + protozoal coverage) |
|---|---|
| Механізм дії | Nitroimidazole prodrug that diffuses passively into bacteria and protozoa, where the low redox potential of anaerobic / microaerophilic organisms reduces its 5-nitro group to reactive radical intermediates (nitroso, hydroxylamine). These intermediates damage DNA via strand breakage and helix destabilization, producing bactericidal effect. Aerobic organisms cannot reduce the prodrug efficiently — hence the selective anaerobic spectrum. Active against Bacteroides fragilis group, Clostridioides spp. (including C. difficile and C. perfringens), Fusobacterium, Peptostreptococcus, Prevotella, and the protozoa Trichomonas, Giardia, Entamoeba histolytica. NO activity against aerobic bacteria. Standard add-on for anaerobic coverage in intra-abdominal, gynecologic, and dental infections, often paired with cefepime or aztreonam in febrile neutropenia with suspected intra-abdominal source. FDA-appr... |
| Типове дозування | Anaerobic infection / FN add-on (adult): 500 mg IV every 8 hours via 30-60 min infusion (or 500 mg PO q8h if able to tolerate oral — >90% bioavailability). Pediatric: 7.5 mg/kg IV/PO q6h, max 4 g/day. C. difficile colitis: 500 mg PO q8h × 10-14 days (mild-moderate; vancomycin oral preferred for severe). Renal: no major adjustment for CrCl ≥10 (but accumulate in anuric patients — give post-dialysis on HD days, reduce to q12h on CRRT). Hepatic impairment: reduce dose by 50% in severe (Child-Pugh C). Duration in FN combinations: matched to primary β-lactam, typically 7-14 days. Maximum continuous duration ≤10 days where possible due to peripheral neuropathy risk with prolonged use. |
| Зареєстровано в Україні | True |
| Відшкодовується НСЗУ | True |
| Остання перевірка для України | 2026-04-27 |
Застереження
- Carcinogenic in mice and rats; epidemiologic data in humans inconclusive but FDA-listed; minimize unnecessary exposure and prolonged courses
Нотатки
Cheap, ubiquitous, narrow-spectrum anaerobic coverage. In febrile neutropenia, added when intra-abdominal or perirectal source is suspected (classic context: severe mucositis with abdominal pain, perianal cellulitis / abscess, typhlitis / neutropenic enterocolitis) and the primary β-lactam lacks anaerobic activity (cefepime, aztreonam, ceftriaxone). NOT needed when pip-tazo or meropenem is the primary agent — these already cover anaerobes. CRITICAL interactions: warfarin (INR doubles — pre-emptively halve warfarin); alcohol (disulfiram-like reaction including IV preparations containing ethanol excipient — read drug labels). Peripheral neuropathy is the limiting toxicity for prolonged use (≥4-6 weeks) — often persistent even after discontinuation; minimize duration. C. difficile colitis: oral metronidazole 500 mg q8h is acceptable for mild-moderate disease but oral vancomycin (or fidaxomicin) is preferred for severe (WBC >15,000, creatinine ≥1.5×) per IDSA 2017. Ukraine: cheap and ubiquitous; NSZU-covered.
Де використовується
У YAML-корпусі не знайдено зворотних посилань.