Evidence map›Paper›PMID 41328133›Full record

ArticleCureus2025

Mefenamic Acid Poisoning Revisited: Central Nervous System Toxicity and Acute Kidney Injury.

Fumiya Inoue, Yuji Okazaki, Toshihisa Ichiba, Akira Namera

Abstract readCase Reports
In one paragraph

Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Fumiya InoueDepartment of Emergency Medicine, Hiroshima City Hiroshima Citizens Hospital, Hiroshima, JPN.
Yuji OkazakiDepartment of Emergency Medicine, Hiroshima City Hiroshima Citizens Hospital, Hiroshima, JPN.
Toshihisa IchibaDepartment of Emergency Medicine, Hiroshima City Hiroshima Citizens Hospital, Hiroshima, JPN.
Akira NameraDepartment of Forensic Medicine, Hiroshima University, Hiroshima, JPN.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nonsteroidal anti-inflammatory drugs (NSAIDs) are a common cause of acute poisoning and often perceived as relatively benign in overdose. Mefenamic acid is unique among NSAIDs in that it is not available over-the-counter in many countries and may have a higher risk of central nervous system toxicity than other NSAIDs. Despite previous reports of seizures and renal dysfunction due to mefenamic acid poisoning, detailed information on the toxicity and the blood concentrations in recent case reports remains limited. A 22-year-old woman presented with two episodes of generalized tonic-clonic seizures three hours after intentional ingestion of multiple analgesics, including 2.5 g (60 mg/kg) of mefenamic acid. On admission, she was agitated but neurologically intact. Initial laboratory findings showed normal renal function. She was admitted for observation. On day 3, she developed acute kidney injury (AKI) with a peak creatinine of 4.21 mg/dL. Her renal dysfunction gradually resolved without dialysis. Drug concentration analysis showed a serum mefenamic acid level of 42.2 µg/mL at admission (toxic threshold: 25 µg/mL). Based on clinical findings and drug concentrations, seizures and AKI were attributed to mefenamic acid poisoning. Mefenamic acid poisoning can result in neurological and renal complications even at modest doses. Given its common use in dysmenorrhea and overlapping demographic with at-risk populations for overdose, clinicians should maintain a high index of suspicion and monitor closely when mefenamic acid ingestion is suspected. Further reports are needed to clarify relationships between serum concentrations, ingested dose, and clinical severity.

Indexed as

acute kidney injurydrug concentrationmefenamic acidseizureself poisoning

Identifiers

PMID41328133
PMCPMC12665362

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.