# Metronidazole-Induced Neurotoxicity: A Case Report

**Authors:** Inês L Caetano, Ana C Cunha, Guiomar Pinheiro, Sónia Chan, Luísa S Pinto

PMC · DOI: 10.7759/cureus.102617 · Cureus · 2026-01-30

## TL;DR

A 70-year-old woman developed neurological symptoms after prolonged metronidazole treatment, which improved after stopping the drug, highlighting the rare but serious neurotoxicity risk of this antibiotic.

## Contribution

This case report adds to the clinical understanding of metronidazole-induced neurotoxicity and emphasizes the importance of timely recognition.

## Key findings

- The patient showed neurological symptoms including confusion, ataxia, and dysarthria after extended metronidazole use.
- MRI revealed a lesion in the splenium of the corpus callosum, consistent with metronidazole-induced neurotoxicity.
- Discontinuation of metronidazole led to progressive neurological improvement.

## Abstract

Metronidazole, a commonly prescribed antibiotic to treat anaerobic and some protozoal infections, can lead to the development of serious, albeit rare, neurological toxicity, particularly in the setting of prolonged treatment and high cumulative dose.

We describe the case of a female patient in her 70s hospitalized for a hepatic abscess who received an extended course of metronidazole and subsequently developed confusion, prostration, dysarthria, ataxia, dysmetria, tremor of the head and upper limbs, diplopia, and nystagmus. Given the suspicion of an adverse drug reaction, metronidazole was discontinued, resulting in progressive neurological improvement. Brain MRI revealed a T2- and T2-fluid-attenuated inversion recovery (FLAIR) hyperintense lesion involving the splenium of the corpus callosum, compatible with metronidazole-induced neurotoxicity in this clinical setting.

This case highlights that, despite being uncommon, metronidazole-induced neurotoxicity should be considered in patients who develop new neurological symptoms during treatment with this drug, promoting timely recognition.

## Linked entities

- **Chemicals:** metronidazole (PubChem CID 4173)
- **Diseases:** hepatic abscess (MONDO:0700051)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** pyogenic abscesses (MESH:D001922), cerebellar dysfunction (MESH:D002526), fever (MESH:D005334), seizure (MESH:D012640), neurological deficits (MESH:D009461), infectious (MESH:D003141), cytotoxic lesions of the corpus callosum (MESH:D061085), neurological deterioration (MESH:D009422), aortic stenosis (MESH:D001024), obesity (MESH:D009765), hemorrhage (MESH:D006470), ataxic gait (MESH:D020234), nausea, vomiting (MESH:D020250), cochleotoxicity (MESH:D000081015), axonal degeneration (MESH:D009410), hepatic encephalopathy (MESH:D006501), confusion (MESH:D003221), prostration (MESH:D006359), acute kidney injury (MESH:D058186), downbeat nystagmus (MESH:D009759), peripheral neuropathy (MESH:D010523), dysarthria (MESH:D004401), Marchiafava-Bignami disease (MESH:D054319), peritoneal irritation (MESH:D010538), posterior circulation stroke (MESH:D020520), gastrointestinal intolerance (MESH:D005767), Neurotoxicity (MESH:D020258), peripheral venous insufficiency (MESH:D014689), neuroinflammatory (MESH:D000090862), chronic kidney disease (MESH:D051436), Wernicke's encephalopathy (MESH:D014899), anorexia (MESH:D000855), leukocytosis (MESH:D007964), abdominal pain (MESH:D015746), weight loss (MESH:D015431), urinary tract infection (MESH:D014552), liver cirrhosis (MESH:D008103), postural instability (MESH:D054972), nephrolithiasis (MESH:D053040), protozoal infections (MESH:D020808), Abscess (MESH:D000038), inflammatory (MESH:D007249), dysmetria (MESH:D002524), hepatic abscess (MESH:D008100), toxic-metabolic encephalopathies (MESH:D001928), ascites (MESH:D001201), neutrophilia (MESH:C563010), head and upper limb tremor (MESH:D014202), malnutrition (MESH:D044342), dyslipidemia (MESH:D050171), visual impairment (MESH:D014786), diplopia (MESH:D004172), ataxia (MESH:D001259), demyelination (MESH:D003711), pain (MESH:D010146), encephalopathies (MESH:D001927), hypertension (MESH:D006973)
- **Chemicals:** reactive oxygen species (MESH:D017382), nitric oxide (MESH:D009569), creatinine (MESH:D003404), amoxicillin/clavulanate (MESH:D019980), thiamine (MESH:D013831), piperacillin-tazobactam (MESH:D000077725), urea (MESH:D014508), ceftriaxone (MESH:D002443), Metronidazole (MESH:D008795), nitroimidazole (MESH:D009593), oxygen (MESH:D010100)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

15 references — full list in the complete paper: https://tomesphere.com/paper/PMC12949957/full.md

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Source: https://tomesphere.com/paper/PMC12949957