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Metronidazole: uses, dosing, side effects & brands

Metronidazole is a nitroimidazole antimicrobial sold in the U.S. under 16 brand and generic names, for abscess, amebiasis and bacteroides infections. Below: what the FDA label says, every product that contains it, what the pills look like, and its recall record.

By the pharmaranks editorial teamReviewed against the FDA (openFDA label, NDC Directory & Enforcement) sourcesUpdated Jul 24, 2026How we research

Key facts

Drug class
Nitroimidazole Antimicrobial
Treats (across its forms)
Abscess, Amebiasis and Bacteroides Infections
Available as
Capsule · Tablet, extended release · Topical · Injectable · Suspension · Solution · Tablet
Sold as
16 products — Flagyl, Flagyl ER and Vandazole, and others
Prescription?
Prescription only
Generic available?
Yes
Half-life
about 8 hours
What the pharmacy pays
about $0.10 per gm — not your price
Boxed warning
Boxed warning

How Vandazole is dosed

From the FDA label for Vandazole (application NDA021806). Other metronidazole products — different forms, different strengths — are dosed differently. Follow the label for the one you were prescribed.

The recommended dose is one applicator full of VANDAZOLE, (approximately 5 grams of gel containing approximately 37.5 mg of metronidazole) administered intravaginally once a day for 5 days. For once a day dosing, VANDAZOLE should be administered at bedtime [see Patient Counseling Information ( 17.4 )] . Not for ophthalmic, dermal, or oral use. One applicator full of VANDAZOLE administered intravaginally once a day for 5 days. ( 2 ) Not for ophthalmic, dermal, or oral use. ( 2 )

Everything below is the FDA label for Vandazole (topical). Metronidazole is also sold as capsule, tablet, extended release, injectable, suspension, solution and tablet, and those are different medicines to take — follow the label for the one you were prescribed.

Vandazole side effects

Adverse reactions occurring in ≥ 1% of patients are: fungal infection, headache, pruritus, abdominal pain, nausea, dysmenorrhea, pharyngitis, rash, infection, diarrhea, breast pain, and metrorrhagia. ( 6.1 ) To report SUSPECTED ADVERSE REACTIONS, contact Teva Pharmaceuticals USA, Inc. at 1-888-838-2872 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. 6.1 Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. The data described below reflect exposure to VANDAZOLE compared to another formulation of vaginal metronidazole in 220 women in a single trial. The population was non-pregnant females (age range 18 to 72 years, the mean was 33 years +/- 11 years) with bacterial vaginosis. The racial demographic of those enrolled was 71 (32%) of White, 143 (65%) of Black, 3 (1%) of Hispanic, 2 (1%) of Asian, and 1 (0%) of other. Patients administered an applicator full of VANDAZOLE intravaginally once daily at bedtime for 5 days. There were no deaths or serious adverse reactions related to drug therapy in the clinical trial. VANDAZOLE was discontinued in 5 patients (2.3%) due to adverse reactions. The incidence of all adverse reactions in VANDAZOLE-treated…

Who shouldn’t take Vandazole

History of hypersensitivity to metronidazole, other nitroimidazole derivatives or parabens ( 4 ) Disulfiram: Psychotic reactions have been reported with disulfiram and oral metronidazole; do not administer concurrently with or within the last 2 weeks of disulfiram ( 4.2 , 7.1 ). Alcohol: Disulfiram-like reactions to alcohol have been reported with oral metronidazole; do not consume alcohol during and for at least three days following treatment ( 4.3 , 7.2 ) 4.1 Hypersensitivity The use of VANDAZOLE is contraindicated in patients with a history of hypersensitivity to metronidazole, other nitroimidazole derivatives, or parabens. Reported reactions include urticaria; erythematous rash; Stevens-Johnson Syndrome, toxic epidermal necrolysis, flushing; nasal congestion; dryness of the mouth, vagina, or vulva; fever; pruritus; fleeting joint pains [see Adverse Reactions ( 6.2 )] . 4.2 Psychotic Reaction with Disulfiram Use of oral metronidazole is associated with psychotic reactions in alcoholic patients who were using disulfiram concurrently. Do not administer VANDAZOLE to patients who have taken disulfiram within the last two weeks [see Adverse Reactions ( 6.2 )] . 4.3 Interaction with Alcohol Use of oral metronidazole is associated with a disulfiram-like reaction to alcohol, including abdominal cramps, nausea, vomiting, headaches, and flushing [see Adverse Reactions ( 6.2 )] . Discontinue alcohol consumption during and for at least three days after therapy with VANDAZOLE.

Vandazole drug interactions

The intravaginal administration of a single 5 gram dose of VANDAZOLE results in relatively lower mean systemic exposure to metronidazole that is approximately 2% to 5% of that achieved following a 500 mg oral dose of metronidazole [see Clinical Pharmacology ( 12.3 )] . The following drug interactions were reported for oral metronidazole. Warfarin and other coumarin anticoagulants: Prolonged anticoagulant effects reported with oral metronidazole; monitor INR and prothrombin time. ( 7.3 ) Lithium: Elevated lithium concentrations reported with oral metronidazole; monitor serum concentrations of lithium. ( 7.4 ) 7.1 Disulfiram Use of oral metronidazole has been associated with psychotic reactions in alcoholic patients who are using disulfiram concurrently. VANDAZOLE should not be used by patients who have taken disulfiram within the last two weeks [see Contraindications ( 4.2 )] . 7.2 Alcoholic Beverages Use of oral metronidazole has been associated with a disulfiram-like reaction (abdominal cramps, nausea, vomiting, headaches, and flushing) to alcohol. Alcoholic beverages and preparations containing ethanol or propylene glycol should not be consumed during and for at least three days after VANDAZOLE therapy [see Contraindications ( 4.3 )] . 7.3 Coumarin and Other Oral Anticoagulants Use of oral metronidazole has been reported to potentiate the anticoagulant effect of warfarin and other coumarin anticoagulants, resulting in a prolongation of prothrombin time. This possible drug interaction should be considered when VANDAZOLE is prescribed for patients on this type of anticoagulant therapy. In patients on oral anticoagulants, consider monitoring prothrombin time, international normalized ratio (INR), and other coagulation parameters while on VANDAZOLE. 7.4 Lithium Short-term use of oral metronidazole has been associated with elevation of serum lithium concentrations and, in a few cases signs of lithium toxicity, in patients stabilized on relatively high doses of lithium. Use VANDAZOLE with caution in patients treated with lithium and consider monitoring lithium serum concentrations while on VANDAZOLE. 7.5 Cimetidine Use of oral metronidazole with cimetidine may prolong the half-life and decrease plasma clearance of metronidazole. No dose adjustment of VANDAZOLE is necessary.

Can you take metronidazole with…?

Source-cited answers for the combinations people actually ask about — each with a verdict and what to watch for.

Metronidazole and food

Every metronidazole product we track (16)

Same active ingredient — different manufacturer, form, price and FDA recall record. That last one is what our independent score measures.

Metronidazole products
#DrugRatingPharmacy pays
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What metronidazole pills look like

Imprint codes, colour and shape from the FDA’s labelling data. Match the imprint on your pill — or search any imprint.

Metronidazole pill imprints
ImprintStrengthColourShape
U;227500 mgwhiteoval
U;227500 mgwhiteoval
MCR;104250 mgwhiteround
U;227500 mgwhiteoval

Combination products containing metronidazole

A combination is a different drug — different dosing, different warnings. It is listed here so you can find it, not so you can substitute it.

How long metronidazole keeps

No metronidazole label we read sets a separate limit for after opening, but they do specify how it must be stored — and the stability behind any date assumes those conditions.

Does metronidazole expire? The in-use limits and storage rules from its labels

Metronidazole and breastfeeding

From LactMed, the US National Library of Medicine’s Drugs and Lactation Database — quoted, not rewritten.

With maternal intravenous and oral therapy, breastfed infants receive metronidazole in doses that are less than those used to treat infections in infants, although the active metabolite adds to the total infant exposure. Plasma levels of the drug and metabolite are measurable, but less than maternal plasma levels. Case reports of Candida infections and diarrhea have been reported, and a comparative trial suggested that oral and rectal colonization with Candida might be more common in infants exposed to metronidazole.

Full LactMed record for metronidazole: levels in milk, effects in breastfed infants, and the drugs it would consider instead

National Institute of Child Health and Human Development, record revised March 15, 2026. LactMed states its information is not a substitute for professional judgement.

What people report to the FDA about metronidazole

The FDA Adverse Event Reporting System (FAERS) collects reports from patients and clinicians. It holds 52,138 reports naming metronidazole, and the FDA flagged 86% of those reports as serious. The effects reported most often — leaving out reports about overdose, misuse or the condition being treated, which dominate the raw list for common medicines:

  • nausea3,743 reports
  • diarrhoea2,953 reports
  • vomiting2,511 reports
  • headache2,493 reports
  • pyrexia2,458 reports
  • abdominal pain2,230 reports
  • fatigue2,123 reports
  • dizziness1,899 reports

Read these as a signal, not a rate. A report does not mean metronidazole caused the effect — anyone can file one, and many describe people taking several medicines for several conditions. Crucially there is no denominator: FAERS does not record how many people took the drug, so these counts cannot be turned into “X% of patients” — a bigger number often just means a more widely used or more talked-about drug. Duplicates exist, and publicity drives reporting. For what is actually established, read the FDA label section above.

Source: openFDA drug/event (FAERS), retrieved August 25, 2026.

How long metronidazole stays in your system

The elimination half-life of metronidazole is about 8 hours. This is the average for healthy adults with normal kidney and liver function; the half-life is much longer in newborns (roughly 22 to 109 hours, longer the more premature the baby). Metronidazole has an active metabolite (hydroxy-metronidazole) whose levels build up in older adults (40-80% higher) and in severe kidney disease, though the label does not give a separate half-life for it.

FLAGYL (metronidazole) label, DailyMed

Half-life is how long the body takes to clear half a dose. It is not the same as how long a drug test can detect it, and it varies with age, kidney and liver function.

Can you drink alcohol on metronidazole?

The label says do not

The label warns against alcohol. Drinking alcoholic beverages (or taking products containing propylene glycol) during metronidazole therapy, or for at least 3 days after, can cause a disulfiram-like reaction: abdominal cramps, nausea, vomiting, headaches, and flushing. This is cross-referenced to the CONTRAINDICATIONS section. The label separately notes that psychotic reactions have occurred in patients using metronidazole and disulfiram together, and it should not be given to anyone who has taken disulfiram within the prior two weeks.

Metronidazole Tablets - DailyMed Label

Is metronidazole safe during pregnancy?

The label reports no clear risk

The label states there are no adequate and well-controlled studies in pregnant women, but published case-control, cohort, and two meta-analyses covering more than 5,000 pregnant women (many with first-trimester exposure) mostly did not show an increased risk of congenital anomalies or other adverse fetal outcomes. One study suggested an increased risk of cleft lip (with or without cleft palate) that was not confirmed in later work. Metronidazole crosses the placenta and its effects on human fetal organogenesis are not known; animal reproduction studies at doses similar to the maximum human dose showed no evidence of fetal harm. The label does not establish a clear risk. Anyone who is or may become pregnant should discuss use with their prescriber.

This is what metronidazole’s FDA label says — not a recommendation to take or stop it. In pregnancy, that decision is your prescriber’s; do not start or stop a medicine on your own.

Metronidazole - DailyMed FDA Label

Related guides

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Frequently asked questions

What is Vandazole?

Vandazole (Metronidazole) is a nitroimidazole antimicrobial used to treat Abscess, Amebiasis, Bacteroides Infections, Bacterial Endocarditis.

What kind of drug is metronidazole?

The FDA classifies metronidazole as a nitroimidazole antimicrobial. Nitroimidazole antibiotics (such as metronidazole) are activated inside oxygen-free bacteria and parasites, where they turn into reactive forms that break and destabilize the microbe's DNA. This kills the germ while largely sparing the body's own cells. If you are checking whether it is safe to combine with something else, the class is what matters — two drugs from the same class usually should not be stacked.

Is metronidazole safe during pregnancy?

The label states there are no adequate and well-controlled studies in pregnant women, but published case-control, cohort, and two meta-analyses covering more than 5,000 pregnant women (many with first-trimester exposure) mostly did not show an increased risk of congenital anomalies or other adverse fetal outcomes. One study suggested an increased risk of cleft lip (with or without cleft palate) that was not confirmed in later work. Metronidazole crosses the placenta and its effects on human fetal organogenesis are not known; animal reproduction studies at doses similar to the maximum human dose showed no evidence of fetal harm. The label does not establish a clear risk. Anyone who is or may become pregnant should discuss use with their prescriber. This is what metronidazole's FDA label says; whether to use it in pregnancy is your prescriber's decision.

Can you drink alcohol while taking metronidazole?

The label warns against alcohol. Drinking alcoholic beverages (or taking products containing propylene glycol) during metronidazole therapy, or for at least 3 days after, can cause a disulfiram-like reaction: abdominal cramps, nausea, vomiting, headaches, and flushing. This is cross-referenced to the CONTRAINDICATIONS section. The label separately notes that psychotic reactions have occurred in patients using metronidazole and disulfiram together, and it should not be given to anyone who has taken disulfiram within the prior two weeks. This is what metronidazole's FDA label says; alcohol advice depends on your dose and health, so confirm with your pharmacist.

How long does metronidazole stay in your system?

The elimination half-life of metronidazole is about 8 hours — that is how long the body takes to clear half of a dose. This is the average for healthy adults with normal kidney and liver function; the half-life is much longer in newborns (roughly 22 to 109 hours, longer the more premature the baby). Metronidazole has an active metabolite (hydroxy-metronidazole) whose levels build up in older adults (40-80% higher) and in severe kidney disease, though the label does not give a separate half-life for it. Half-life is not the same as how long a drug test can detect the drug, and it varies with age, kidney and liver function.

Can you take metronidazole with other medicines?

It depends on the medicine. We check it against the FDA labels rather than guessing: our interaction checker searches each drug's own label for the other and quotes what it says, naming the section it came from. Run metronidazole against whatever else you take — and remember that a label not naming a drug is not the same as that combination being safe.

What brand names is metronidazole sold under?

We track 16 metronidazole-containing products in the U.S.: Flagyl, Flagyl ER, Vandazole, Flagyl I.V. Rtu in Plastic Container, Likmez, Metro I.V., Metro I.V. in Plastic Container and Metrocream, and 8 more. They are the same active ingredient; they differ in form, manufacturer, price and FDA recall record.

What forms does metronidazole come in?

Across the brands we track, metronidazole is currently marketed as capsule, tablet, extended release, topical, injectable, suspension, solution and tablet, per the FDA's National Drug Code Directory. Each form is dosed differently — follow the label for the exact product you were prescribed.

Is there a generic metronidazole?

Yes. Our catalog lists 2 generic metronidazole products alongside the brand versions. A generic has the same active ingredient and must meet the FDA's bioequivalence standard; it usually costs less. Ask your pharmacist which one your plan covers.

What should I avoid while taking metronidazole?

Alcohol: the FDA label contraindicates drinking on it — see the alcohol section above for what it actually says. Food: beer, wine, spirits, and other products containing alcohol — see the food section above for what each one does and whether it means avoiding it or just being consistent. Other medicines: we hold source-cited interaction answers for Can you drink alcohol while taking metronidazole (Flagyl)?. This is what the FDA label and our cited sources say — it is not a complete list. Your pharmacist can check your own combination.

What are the most common side effects of Flagyl (metronidazole)?

The most common side effects of Flagyl (metronidazole) are nausea, a sharp, unpleasant metallic taste, headache, loss of appetite, diarrhea, stomach cramps, dry mouth, and a furry or irritated tongue. MedlinePlus lists nausea, vomiting, diarrhea, stomach cramps, loss of appetite, headache and a "sharp, unpleasant metallic taste" among the drug's expected effects. A minority of people notice darkened or reddish-brown urine; the FDA Flagyl label reports this in roughly 1 in 100,000 patients and states it is "almost certainly a metabolite of metronidazole and seems to have no clinical significance" — so it is harmless and fades once you finish the course.

Why can't I drink alcohol while taking Flagyl (metronidazole)?

Do not drink any alcohol while taking Flagyl (metronidazole) and for at least 3 days after your last dose. Metronidazole interferes with how your body breaks down alcohol and can trigger a disulfiram-like reaction. MedlinePlus warns to "not drink alcoholic beverages or take products with alcohol or propylene glycol while taking this medication and for at least 3 days after your final dose," because the combination causes "nausea, vomiting, stomach cramps, headache, sweating, and flushing." The reaction can also include a pounding or racing heartbeat and difficulty breathing. Avoid hidden alcohol too — in cough syrups, some mouthwashes, tonics, and elixirs.

When should I call a doctor or get emergency care while on Flagyl (metronidazole)?

Call your doctor right away or seek urgent care if you develop numbness, tingling, or burning pain in your hands or feet, or any seizure. MedlinePlus lists "numbness, pain, burning, or tingling in your hands or feet" and "seizures" as effects needing immediate medical attention, and the FDA Flagyl label describes these as peripheral neuropathy and convulsive seizures that call for prompt discontinuation under a doctor's direction. Also seek urgent help for a serious allergic reaction (rash, hives, blistering or peeling skin, swelling, trouble breathing), signs of aseptic meningitis (stiff neck, fever, severe headache), or severe, watery or bloody diarrhea with stomach cramps — a possible sign of Clostridioides difficile (C. difficile) infection, a known risk with nearly all antibiotics. Do not stop a prescribed antibiotic on your own; contact your prescriber, who will decide whether to stop it.

Does Flagyl (metronidazole) have a cancer warning, and should long courses worry me?

Flagyl (metronidazole) carries an FDA boxed warning that reads: "Metronidazole has been shown to be carcinogenic in mice and rats. Unnecessary use of the drug should be avoided. Its use should be reserved for the conditions described in the INDICATIONS AND USAGE section." This is why doctors prescribe it only for confirmed or strongly suspected infections and for short courses — a standard 7-to-10-day treatment is not the unnecessary, prolonged, high-dose animal exposure the warning is based on, and no cause-and-effect link has been established in people. The more practical concern with long or repeated courses is nerve damage (peripheral neuropathy), so tell your doctor if you have taken metronidazole many times before.

When do Flagyl (metronidazole) side effects start, and how long do they last?

Effects such as nausea and the metallic taste often appear within the first day or two of starting Flagyl (metronidazole) and usually ease within a few days after you finish the course; the metallic taste and any urine darkening resolve once the drug clears your system (its half-life is about 8 hours). Take the full course exactly as prescribed even once you feel better — MedlinePlus advises: "Continue to take this medication even if you feel well... If you stop taking this medication too soon or skip doses, your infection may not be completely treated and the bacteria may become resistant to antibiotics." This is not a complete list of side effects; ask your pharmacist or prescriber about anything unexpected or persistent.

Cite this page
APA
pharmaranks. (2026, July 24). Metronidazole: uses, dosing, side effects & brands. https://pharmaranks.com/drugs/metronidazole
MLA
“Metronidazole: uses, dosing, side effects & brands.” pharmaranks, 24 July 2026, https://pharmaranks.com/drugs/metronidazole.

We summarise public FDA and NIH sources — for a clinical claim, cite the primary source we link to as well.

Sources: FDA openFDA drug label, National Drug Code Directory, and Enforcement (recall) database. This page reproduces public FDA data and is not medical advice. Dosing is set by your prescriber.

Read the full FDA label for metronidazole on DailyMed (NIH) ↗ — including its boxed warning in full.