Evidence map›Paper›PMID 42031672›Full record

ArticleBritish journal of clinical pharmacology2026

A prospective series of acute rivaroxaban overdose, coagulopathy and bleeding complications (ATOM 11).

Katherine Z Isoardi, Angela L Chiew, Keith Harris, Geoffrey K Isbister

Abstract read
In one paragraph

Article in British journal of clinical pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

What it found

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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

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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

1 citing paper in PubMed.

  1. Article
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.

Katherine Z IsoardiClinical Toxicology Unit, Princess Alexandra Hospital, Brisbane, Australia.ORCID https://orcid.org/0000-0002-1176-7923
Angela L ChiewClinical Toxicology Unit, Prince of Wales Hospital, Sydney, Australia.ORCID https://orcid.org/0000-0002-0079-5056
Keith HarrisClinical Toxicology Unit, Princess Alexandra Hospital, Brisbane, Australia.ORCID https://orcid.org/0000-0003-0724-1088
Geoffrey K IsbisterDepartment of Clinical Toxicology, Calvary Mater Newcastle Hospital, Newcastle, Australia.ORCID https://orcid.org/0000-0003-1519-7419

Funding

National Health and Medical Research Council ID 2016380
6 · The paper itself

Abstract

aimThere is limited research describing rivaroxaban overdose. We aim to describe rivaroxaban overdose, coagulopathy and bleeding complications.

methodsThis is a prospective series of acute adult (>14 years) rivaroxaban overdose presentations >40 mg enrolled in the Australian Toxicology Monitoring study and presenting to three Australian clinical toxicology units from August 2014 to August 2024. Data collected included demographics, ingestion details, coagulation profile, rivaroxaban concentrations, significant bleeding (with haemoglobin decrement) and outcome.

resultsThere were 58 presentations in 52 patients, 29/52 (56%) males, median age of 49 years (range: 18-93 years). The median reported dose ingested was 200 mg (IQR: 92.5-400 mg, range: 45-1120 mg). Co-ingestants were taken in 49 (84%), most commonly mirtazapine and paracetamol. A raised international normalized ratio (INR) of >1.5 occurred in 46 (79%) with a median peak INR of 2.5 (IQR: 1.7-3.7). The median duration for an elevated INR to return to ≤1.5 was 22 h (IQR: 14-38 h). Significant bleeding occurred in two patients; both were managed conservatively without factor replacement. Rivaroxaban concentrations were available in 11 cases. There was a strong correlation (R

conclusionBleeding was uncommon following rivaroxaban overdose. The INR appears to be a good indicator of coagulopathy, with an INR of ≤1.5 approximating therapeutic rivaroxaban concentrations. Observation of patients following acute rivaroxaban overdose until the INR ≤ 1.5 seems reasonable.

Indexed as

Blood Coagulation DisordersDrug OverdoseFactor Xa InhibitorsHemorrhageRivaroxabanAdolescentAdultAgedAged, 80 and overAustraliaFemaleHumansInternational Normalized RatioMaleMiddle AgedProspective StudiesFactor Xa InhibitorsRivaroxabanbleeding complicationscoagulopathydirect oral anticoagulants (DOACs)overdoserivaroxaban

Identifiers

PMID42031672
PMCPMC13420894

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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.