metronidazole(redirected from acea)
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Pharmacologic class: Nitroimidazole derivative
Therapeutic class: Anti-infective, antiprotozoal
Pregnancy risk category B
FDA Box Warning
• Drug is carcinogenic in mice and rats. Avoid unnecessary use; reserve drug for indicated conditions.
Disturbs DNA synthesis in susceptible bacterial organisms
Capsules: 375 mg
Powder for injection: 5 mg/ml, 500-mg vials
Premixed injection: 500 mg/100 ml
Tablets: 250 mg, 500 mg
Tablets (extended-release): 750 mg
Topical cream, topical gel: 0.75% in 28.4-g tubes
Topical lotion: 0.75% in 59-ml bottle
Vaginal gel: 0.75% (37.5 mg/5-g applicator) in 70-g tubes
Indications and dosages
Adults: 2 g P.O. as a single dose or in two 1-g doses given on same day. Alternatively, 500 mg P.O. b.i.d. for 7 days.
➣ Bacterial infections
Adults: Initially, 15 mg/kg I.V., followed by 7.5 mg/kg I.V. q 6 hours, not to exceed 4 g/day for 7 to 10 days
Adults: 750 mg P.O. q 8 hours for 5 to 10 days
➣ Amebic liver abscess
Adults: 500 to 750 mg P.O. t.i.d. for 5 to 10 days. If drug can't be given orally, administer 500 mg I.V. q 6 hours for 10 days.
Children: 35 to 50 mg/kg/day P.O. in three divided doses for 10 days, to a maximum of 750 mg/dose
➣ Bacterial vaginosis
Adults: In nonpregnant patients, 750 mg/day P.O. (extended-release) for 7 days or 5 g of 0.75% vaginal gel b.i.d. for 5 days. In pregnant patients, 250 mg P.O. t.i.d. for 7 days.
➣ Perioperative prophylaxis in colorectal surgery
Adults: Initially, 15 mg/kg I.V. infusion over 30 to 60 minutes, completed 1 hour before surgery; if necessary, 7.5 mg/kg I.V. infusion over 30 to 60 minutes at 6 and 12 hours after initial dose
Adults: Rub a thin layer of topical lotion, gel, or cream onto entire affected area morning and evening. Improvement should occur within 3 weeks.
• Hypersensitivity to drug, other nitroimidazole derivatives, or parabens (topical form only)
• First-trimester pregnancy in patients with trichomoniasis
Use cautiously in:
• severe hepatic impairment
• history of blood dyscrasias, seizures, or other neurologic problems
• breastfeeding patients
• Reconstitute powder for injection by adding 4.4 ml of sterile or bacteriostatic water for injection, 0.9% sodium chloride injection, or bacteriostatic sodium chloride injection to 500-mg vial. Further dilute resulting
concentration (100 mg/ml) in 0.9% sodium chloride injection, 5% dextrose injection, or lactated Ringer's injection solution to a concentration of 8 mg/ml or less. Infuse each I.V. dose over 1 hour.
• Be aware that for I.V. injection, drug need not be diluted or neutralized.
• Don't use equipment containing aluminum to reconstitute or transfer reconstituted solution to diluent; solution may turn reddish-brown.
• Don't interchange vaginal gel with topical gel, cream, or lotion.
CNS: dizziness, headache, ataxia, vertigo, incoordination, insomnia, fatigue
EENT: rhinitis, sinusitis, pharyngitis
GI: nausea, vomiting, diarrhea, abdominal pain, furry tongue, glossitis, dry mouth, anorexia
GU: dysuria, dark urine, incontinence
Skin: rash, urticaria, burning, mild skin dryness, skin irritation, transient redness (with topical forms)
Other: unpleasant or metallic taste, superinfection, phlebitis at I.V. site
Drug-drug. Azathioprine, fluorouracil: increased risk of leukopenia
Cimetidine: decreased metronidazole metabolism, increased risk of toxicity
Disulfiram: acute psychosis and confusion
Lithium: increased lithium blood level
Phenobarbital: increased metronidazole metabolism, decreased efficacy
Warfarin: increased warfarin effects
Drug-diagnostic tests. Alanine aminotransferase, aspartate aminotransferase, lactate dehydrogenase: altered levels
Drug-behaviors. Alcohol use: disulfiram-like reaction
• Monitor I.V. site. Avoid prolonged use of indwelling catheter.
• Evaluate hematologic studies, especially in patients with history of blood dyscrasias.
• Advise patient to take drug with food if it causes GI upset. However, instruct him to take extended-release tablets 1 hour before or 2 hours after meals.
• Tell patient with trichomoniasis to refrain from sexual intercourse or to have male partner wear a condom to prevent reinfection. Explain that asymptomatic sex partners should be treated simultaneously.
• Advise patient to report fever, sore throat, bleeding, or bruising.
• Inform patient that drug may cause metallic taste and may discolor urine deep brownish-red.
• Tell patient using topical form to clean area thoroughly with mild cleanser before use and then wait 15 to 20 minutes before applying drug. Tell her she may apply cosmetics to skin after applying drug; with topical lotion, instruct her to let skin dry at least 5 minutes before applying cosmetics.
• Tell female patient to consult prescriber if she is pregnant or plans to become pregnant.
• As appropriate, review all other significant and life-threatening adverse reactions and interactions, especially those related to the drugs, tests, and behaviors mentioned above.
metronidazole/met·ro·ni·da·zole/ (-ni´dah-zōl) an antiprotozoal and antibacterial effective against obligate anaerobes; used as the base or the hydrochloride salt. It is also used as a topical treatment for rosacea.
metronidazoleNoritate® Dermatology An antibiotic used for managing dermatitides and erythema of rosacea. See Rosacea Infectious disease An antibiotic used to treat bacterial, fungal, and parasitic infections; it is the most effective agent for H pylori infections.
metronidazoleAn antibiotic drug effective against Trichomonas vaginalis and Entamoeba histolytica as well as many other organisms. It is especially useful in the treatment of amoebic dysentery and amoebic liver abscesses as well as ANAEROBIC infections. The drug is on the WHO official list. Brand names are Acea Gel, Elyzol, Flagyl, Metrosa and Zidoval. The drug is also formulated with the antifungal drug nystatin under the brand name Flagyl Compak and, for external use only, under the brand names Anabact, Metrogel, Metrotop and Rozex.
metronidazole; Flagyl antibacterial agent effective against anaerobic infections; adult dose = 500mg every 8 hours
n a generic synthetic antibacterial compound available for both oral and intravenous use. It is indicated in the treatment of serious infections caused by susceptible anaerobic bacteria. In dentistry, it is used in the treatment of HIV, periodontal disease, and aggressive periodontitis.
drug class: trichomonacide, amebicide, antiinfective;
action: direct-acting amebicide/trichomonacide binds, degrades DNA in organisms;
uses: intestinal amebiasis, amebic abscess, trichomoniasis, refractory trichomoniasis, bacterial anaerobic infections.