Evidence map›Paper›PMID 35209830›Full record

ArticleCurrent drug safety2022

Event Monitoring and Evaluation by Community Pharmacists in Japan: A Pilot Study on Fenofibrate and Pemafibrate.

Masao Takahashi, Nobuhiro Ooba, Marina Nagamura, Makoto Ushida, Eiji Kawakami, Masaomi Kimura, Tsugumichi Sato, Yoshinori Takahashi, Junichi Tokuyoshi, Hajime Hashiba and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Current drug safety, 2022. 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
0.4field-weighted citation impact, top 44% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  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

13 authors at 6 institutions in 1 country.

Masao TakahashiDEM Committee, Japan Pharmaceutical Association, Tokyo, Japan.
Nobuhiro OobaDepartment of Clinical Pharmacy, Nihon University School of Pharmacy, Chiba, Japan.
Marina NagamuraDepartment of Clinical Pharmacy, Nihon University School of Pharmacy, Chiba, Japan.
Makoto UshidaFaculty of Pharmacy, Meijo University, Aichi, Japan.
Eiji KawakamiDEM Committee, Japan Pharmaceutical Association, Tokyo, Japan.
Masaomi KimuraDepartment of Computer Science and Engineering, Shibaura Institute of Technology, Tokyo, Japan.
Tsugumichi SatoDepartment of Pharmacy, Faculty of Pharmaceutical Sciences, Tokyo University of Science, Chiba, Japan.
Yoshinori TakahashiDEM Committee, Japan Pharmaceutical Association, Tokyo, Japan.
Junichi TokuyoshiDEM Committee, Japan Pharmaceutical Association, Tokyo, Japan.
Hajime HashibaDEM Committee, Japan Pharmaceutical Association, Tokyo, Japan.
Miwako KameiFaculty of Pharmaceutical Sciences, Teikyo Heisei University, Tokyo, Japan.
Choichiro MiyazakiDEM Committee, Japan Pharmaceutical Association, Tokyo, Japan.
Mitsuaki ShimadaDEM Committee, Japan Pharmaceutical Association, Tokyo, Japan.
Japan Chemical Industry Association · JPNihon University · JPMeijo University · JPShibaura Institute of Technology · JPTeikyo Heisei University · JPTokyo University of Science · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe Japan Pharmaceutical Association has conducted drug event monitoring to detect drug events related to pemafibrate. As there are a few studies on the safety of pemafibrate in clinical settings, a pilot study evaluating the association between drug use and detected events was performed in Japan.

aimsIn this study, the association between detected events and the use of pemafibrate, utilizing pharmacy records maintained by community pharmacists, was investigated. We identified the newuser cohort using a test and active comparison drug and collected the baseline information. An active comparison group comprising new users was used to assess the events.

methodsA retrospective cohort study using questionnaires regarding baseline and event data was conducted by community pharmacists belonging to the Japan Pharmaceutical Association. The incidence of event and estimated hazard ratio were calculated using the Cox proportional hazards model that was adjusted for confounding factors, such as age and sex.

resultsA total of 1294 patients using pemafibrate and 508 patients using fenofibrate were identified as new drug users. The most reported events involving suspected adverse reactions and add-on drugs were increased blood pressure and lipid-lowering effects with pemafibrate use, and nasopharyngitis, pruritus, dizziness, and lipid-lowering effects with fenofibrate use. No significant differences were found in commonly occurring events, except that an add-on anti-hypertensive drug has been used by pemafibrate users compared to fenofibrate users.

conclusionThis study conducted by pharmacists can facilitate the safety assessment of newly marketed drugs, as few drug use investigations with a comparator are carried out by the Japanese authority for pharmaceutical companies. However, further research is required.

Indexed as

FenofibrateBenzoxazolesButyratesHumansJapanPharmaceutical PreparationsPharmacistsPilot ProjectsRetrospective StudiesBenzoxazolesButyratesFenofibratePharmaceutical Preparations(R)-2-(3-((benzoxazol-2-yl-d4 (3-(4-methoxyphenoxy-d7)propyl)amino)methyl)phenoxy) butanoic acidcommunity pharmacistconcurrent controlevent monitoringnew-user designprimary data collectionRetrospective cohort study

Identifiers

PMID35209830
PMCPMC9720878
OpenAlexW4214754942

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.