WARNING
Metronidazole has been shown to be carcinogenic in mice and rats (See PRECAUTIONS). Unnecessary use of the drug should be avoided. Its use should be reserved for the...
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Flagyl® Oral Formulation (metronidazole oral formulation)
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Our scientific content is evidence-based, scientifically balanced and non-promotional. It undergoes rigorous internal medical review and is updated regularly to reflect new information.
Flagyl® Oral Formulation Quick Finder
Indications and Usage
INDICATIONS AND USAGE
Symptomatic Trichomoniasis. FLAGYL 375 capsules are indicated for the treatment of T. vaginalis infection in females...
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Dosage and Administration
DOSAGE AND ADMINISTRATION
Trichomoniasis
In the Female: Seven-day course of treatment (375 mg two times daily for seven consecutive days).
A seven-day course of...
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Contraindications
CONTRAINDICATIONS
Hypersensitivity
FLAGYL 375 capsules are contraindicated in patients with a prior history of hypersensitivity to metronidazole or other...
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Warnings and Precautions
WARNINGS
Hypersensitivity Reactions
Hypersensitivity reactions including toxic epidermal necrolysis (TEN), Stevens-Johnson Syndrome (SJS), drug reaction with...
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Adverse Reactions
ADVERSE REACTIONS
The following reactions have been reported during treatment with metronidazole:
Central Nervous System: The most serious adverse reactions reported in patients treated with...
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Overdosage
OVERDOSAGE
Single oral doses of metronidazole, up to 15 g, have been reported in suicide attempts and accidental overdoses. Symptoms reported include nausea, vomiting, and ataxia.
Oral metronidazole has been studied as...
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Description
DESCRIPTION
FLAGYL (metronidazole) capsules, 375 mg is an oral formulation of the synthetic nitroimidazole antimicrobial agent, 2-methyl-5-nitro-1H-imidazole-1-ethanol, which has the following...
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Clinical Pharmacology
CLINICAL PHARMACOLOGY
Absorption
Disposition of metronidazole in the body is similar for both oral and intravenous dosage forms.
FLAGYL 375 capsules have been...
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How Supplied/Storage and Handling
HOW SUPPLIED
FLAGYL 375 capsules have an iron gray opaque body imprinted with 375 mg and a light green opaque cap imprinted with FLAGYL, supplied as:
NDC Number Size
0025-1942-50 ...
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Report Adverse Event
To report an adverse event related to Pfizer-BioNTech COVID-19 Vaccine (also known as COMIRNATY®, COVID-19 mRNA, Vaccine BNT162b2 or BNT162) or Pfizer COVID-19 Treatment (also known as PAXLOVID™ (nirmatrelvir tablets; ritonavir tablets)), and you are not part of a clinical trial* for this product, click the link below to submit your information:
*If you are involved in a clinical trial for either product, adverse events should be reported to your coordinating study site.
If you cannot use the above website or would like to report an adverse event related to a different Pfizer product, please call Pfizer Safety at(800) 438-1985.
You may also contact the U.S. Food and Drug Administration (FDA) directly to report adverse events or product quality concerns either online at www.fda.gov/medwatchor by calling
(800)-332-1088.
(800)-332-1088.