Evidence map›Paper›PMID 35728952›Full record

ArticleEuropean journal of hospital pharmacy : science and practice2023

Adverse drug reactions of statin therapy in China from 1989 to 2019: a national database analysis.

Leo Tsui, Peiying Ye, Shiling Xu, Yuan Lin, Bin Chen, Sy-Ping Chen, Ruoh-Yi Cheng

Open access · greenAbstract read
In one paragraph

Article in European journal of hospital pharmacy : science and practice, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.1field-weighted citation impact, top 8% of its field
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

9 citing papers in PubMed, 15 citations in OpenAlex.

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  6. Patient versus physician preferences for lipid-lowering drug therapy: A discrete choice experiment.Health expectations : an international journal of public participation in health care and health policy · 2024
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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

7 authors at 3 institutions in 1 country.

Leo Tsui *School of Pharmacy, Shanghai University of Medicine and Health Sciences, Shanghai, People's Republic of China standhavemail@yahoo.com.tw.ORCID 0000-0001-8071-0624
Peiying Ye *School of Pharmacy and Medical Technology, Putian University, Putian, Fujian, People's Republic of China.
Shiling XuSchool of Pharmacy and Medical Technology, Putian University, Putian, Fujian, People's Republic of China.
Yuan LinSchool of Pharmacy and Medical Technology, Putian University, Putian, Fujian, People's Republic of China.
Bin ChenSchool of Pharmacy and Medical Technology, Putian University, Putian, Fujian, People's Republic of China.
Sy-Ping ChenCollege of Medicine, Ningde Normal University, Ningde, Fujian, People's Republic of China.
Ruoh-Yi ChengCollege of Foreign Language, Putian University, Putian, People's Republic of China.
Putian University · CNNingde Normal University · CNShanghai University of Medicine and Health Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe baseline incidence of the adverse events of statin therapy varies between countries. Notably, Chinese patients seem more susceptible to myopathy induced by simvastatin.

objectivesThis research studies the adverse drug reactions (ADRs) of statin therapy in China by analysing trial-based data from the Anti-hyperlipidaemic Drug Database built by the China National Medical Products Administration Information Centre.

methodsAll clinical trials involving statin therapy (including simvastatin, atorvastatin, fluvastatin, lovastatin, pravastatin and rosuvastatin) in China from 1989 to 2019 were screened. In total, 569 clinical studies with 37 828 patients were selected from 2650 clinical trials in the database.

resultsAmong the reported cases with ADRs (2822/37 828; 7.460%), gastrointestinal symptoms were the most common (1491/37 828; 3.942%), followed by liver disease (486/37 828; 1.285%), muscle symptoms (444/37 828; 1.174%) and neurological symptoms (247/37 828; 0.653%). Pravastatin (231/1988; 11.620%) caused the most common gastrointestinal side effects, followed by fluvastatin (333/3094; 10.763%). The least likely to cause gastrointestinal irritation was rosuvastatin (82/1846; 4.442%).

conclusionIn Chinese clinical trials, gastrointestinal symptoms were the most common ADR of statin use for hyperlipidaemia and other cardiovascular diseases.

Indexed as

Drug-Related Side Effects and Adverse ReactionsHydroxymethylglutaryl-CoA Reductase InhibitorsFluvastatinHumansPravastatinRosuvastatin CalciumSimvastatinFluvastatinHydroxymethylglutaryl-CoA Reductase InhibitorsPravastatinRosuvastatin CalciumSimvastatinClinical TrialDRUG-RELATED SIDE EFFECTS AND ADVERSE REACTIONSLipid Metabolism DisordersMetabolic DiseasesSafety

Identifiers

PMID35728952
PMCPMC10086733
OpenAlexW4283207949

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.