Evidence map›Paper›PMID 42665419›Full record

ArticleIn vivo (Athens, Greece)

Infection-related and Hepatobiliary Death Outcome Reports Involving Avacopan in the Japanese Pharmacovigilance Database.

Naohito Ide, Ken-Ichi Sako, Tomoji Maeda

Abstract read
In one paragraph

Article in In vivo (Athens, Greece). 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
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0citing papers in PubMed
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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

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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

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

3 authors.

Naohito IdeDepartment of Clinical Pharmacology, Nihon Pharmaceutical University, Saitama, Japan n-ide@nichiyaku.ac.jp.
Ken-Ichi SakoDepartment of Clinical Pharmacology, Nihon Pharmaceutical University, Saitama, Japan.
Tomoji MaedaDepartment of Clinical Pharmacology, Nihon Pharmaceutical University, Saitama, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimAvacopan is used to treat antineutrophil cytoplasmic antibody-associated vasculitis. In Japan, serious hepatobiliary adverse events, including vanishing bile duct syndrome, have recently become a major safety concern. This study characterized reports with death recorded as the outcome involving avacopan in the Japanese Adverse Drug Event Report database (JADER). PATIENTS AND

methodsReports involving avacopan as a suspected drug and death recorded as the outcome were extracted from JADER. Adverse events were classified by primary system organ class and preferred term. Quarterly reporting trends and time-to-onset were evaluated for hepatobiliary and infection-related adverse events.

resultsA total of 79 reports were identified; 64 involved patients aged ≥70 years. Infections and infestations were the most frequent system organ classes among adverse events with death recorded as the outcome (n=46), followed by hepatobiliary disorders (n=21). Vanishing bile duct syndrome was the most frequent hepatobiliary preferred term (n=13).

conclusionIn JADER, death outcome reports involving avacopan frequently included infection-related and hepatobiliary events. Hepatobiliary events occurred mainly within 90 days, whereas infection-related events showed a broader time-to-onset distribution. These findings suggest the need for early hepatobiliary monitoring and continued attention to serious infections during avacopan treatment.

Indexed as

Drug-Related Side Effects and Adverse ReactionsInfectionsPharmacovigilanceAdverse Drug Reaction Reporting SystemsAgedAged, 80 and overDatabases, FactualFemaleHumansJapanMaleMiddle Agedadverse reactionsAvacopandeath outcomeJapanese Adverse Drug Event Report database

Identifiers

PMID42665419
PMCPMC13531159

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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.