Evidence map›Paper›PMID 40093810›Full record

ArticleInternational journal of medical sciences2025

Data Mining of the FDA Adverse Event Reporting System and Animal Experiments for Assessment of Rhabdomyolysis Risk Associated with Lipid-lowering Drugs.

Shinji Kobuchi, Daisuke Sugiyama, Anna Iima, Ami Obuchi, Ayumi Osaka, Ayana Doi, Hikaru Ueta, Satoshi Yokoyama, Kouichi Hosomi, Mitsutaka Takada and 1 more

Abstract read
In one paragraph

Article in International journal of medical sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

11 authors.

Shinji KobuchiDepartment of Pharmacokinetics, Kyoto Pharmaceutical University, Kyoto 607-8414, Japan.
Daisuke SugiyamaDepartment of Pharmacokinetics, Kyoto Pharmaceutical University, Kyoto 607-8414, Japan.
Anna IimaDepartment of Pharmacokinetics, Kyoto Pharmaceutical University, Kyoto 607-8414, Japan.
Ami ObuchiDepartment of Pharmacokinetics, Kyoto Pharmaceutical University, Kyoto 607-8414, Japan.
Ayumi OsakaDepartment of Pharmacokinetics, Kyoto Pharmaceutical University, Kyoto 607-8414, Japan.
Ayana DoiDepartment of Pharmacokinetics, Kyoto Pharmaceutical University, Kyoto 607-8414, Japan.
Hikaru UetaFaculty of Pharmacy, Kindai University, 3-4-1, Kowakae, Higashi-osaka, Osaka 577-8502, Japan.
Satoshi YokoyamaFaculty of Pharmacy, Kindai University, 3-4-1, Kowakae, Higashi-osaka, Osaka 577-8502, Japan.
Kouichi HosomiFaculty of Pharmacy, Kindai University, 3-4-1, Kowakae, Higashi-osaka, Osaka 577-8502, Japan.
Mitsutaka TakadaFaculty of Pharmacy, Kindai University, 3-4-1, Kowakae, Higashi-osaka, Osaka 577-8502, Japan.
Toshiyuki SakaedaDepartment of Pharmacokinetics, Kyoto Pharmaceutical University, Kyoto 607-8414, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite extensive research on pharmacokinetic interactions between hydroxymethylglutaryl-CoA reductase inhibitors (statins) and fibrates, the underlying pharmacodynamic mechanisms contributing to the increased risk of rhabdomyolysis remain unclear. This study aimed to determine the differences among statins or fibrates in terms of their susceptibility to rhabdomyolysis. The data mining of FDA Adverse Event Reporting System (FAERS) suggested the association of both statins and fibrates with rhabdomyolysis and the add-on effect of their combinations. In rats, their administration was associated with outliers in creatine phosphokinase and myoglobin levels and a larger distribution of data than in the control. Additionally, co-administration of cerivastatin increased the gemfibrozil concentration in skin and muscle tissues by more than two-fold without an increase in systemic exposure to gemfibrozil, suggesting that an alteration in the pharmacokinetics of gemfibrozil might contribute to an increased risk of rhabdomyolysis when cerivastatin and gemfibrozil are co-administered. Taken together, caution is uniformly needed in combination therapy with statins and fibrates because of the increased risk of rhabdomyolysis.

Indexed as

Adverse Drug Reaction Reporting SystemsFibric AcidsHydroxymethylglutaryl-CoA Reductase InhibitorsHypolipidemic AgentsRhabdomyolysisAnimalsCreatine KinaseData MiningDrug InteractionsGemfibrozilHumansMalePyridinesRatsUnited StatesUnited States Food and Drug AdministrationcerivastatinCreatine KinaseFibric AcidsGemfibrozilHydroxymethylglutaryl-CoA Reductase InhibitorsHypolipidemic AgentsPyridinescerivastatinFAERSgemfibrozilpreclinical pharmacokineticsrhabdomyolysis

Identifiers

PMID40093810
PMCPMC11905262

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Registered trials

None linked

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.