Evidence map›Paper›PMID 26660898›Full record

ArticleTherapeutic advances in respiratory disease2016

Pharmacokinetics of consecutive oral moxifloxacin (400 mg/day) in patients with respiratory tract infection.

Fumitaka Ito, Yasushi Ohno, Sayaka Toyoshi, Daizo Kaito, Yanase Koumei, Junki Endo, Fumihiko Kamamiya, Hidenori Mori, Masahiro Mori, Megumi Morishita and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Therapeutic advances in respiratory disease, 2016. 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
1.1field-weighted citation impact, top 20% 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

2 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  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

12 authors at 1 institution in 1 country.

Fumitaka ItoSecond Department of Internal Medicine, Gifu University Graduate School of Medicine, Gifu, Japan.
Yasushi OhnoSecond Department of Internal Medicine, Gifu University Graduate School of Medicine, 1-1 Yanagido, Gifu 501-1194, Japan yasusi@gifu-u.ac.jp.
Sayaka ToyoshiSecond Department of Internal Medicine, Gifu University Graduate School of Medicine, Gifu, Japan.
Daizo KaitoSecond Department of Internal Medicine, Gifu University Graduate School of Medicine, Gifu, Japan.
Yanase KoumeiSecond Department of Internal Medicine, Gifu University Graduate School of Medicine, Gifu, Japan.
Junki EndoSecond Department of Internal Medicine, Gifu University Graduate School of Medicine, Gifu, Japan.
Fumihiko KamamiyaSecond Department of Internal Medicine, Gifu University Graduate School of Medicine, Gifu, Japan.
Hidenori MoriSecond Department of Internal Medicine, Gifu University Graduate School of Medicine, Gifu, Japan.
Masahiro MoriSecond Department of Internal Medicine, Gifu University Graduate School of Medicine, Gifu, Japan.
Megumi MorishitaSecond Department of Internal Medicine, Gifu University Graduate School of Medicine, Gifu, Japan.
Norihiko FunaguchiSecond Department of Internal Medicine, Gifu University Graduate School of Medicine, Gifu, Japan.
Shinya MinatoguchiSecond Department of Internal Medicine, Gifu University Graduate School of Medicine, Gifu, Japan.
Gifu University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A population pharmacokinetic analysis was performed to investigate the pharmacokinetics of moxifloxacin (400 mg) following a once-daily oral administration in 28 patients with respiratory tract infection disease. The maximum plasma concentration and the area under the plasma concentration-time curve were 3.97 µg/ml and 51.74 µg·h/ml, respectively; these values were nearly equivalent to those of healthy adult men. Two adverse drug reactions (nausea, vomiting) occurred, but both reactions were mild and nonserious and the patients recovered without treatment. The pharmacokinetic profile of moxifloxacin in Japanese patients with respiratory tract infection and an underlying disease should thus be considered safe and comparable with that in healthy adult men, and adjustment of dose may do not need for age, sex, body weight, or renal function.

Indexed as

Administration, OralAgedAged, 80 and overAnti-Bacterial AgentsArea Under CurveFemaleFluoroquinolonesHumansJapanMaleMiddle AgedMoxifloxacinRespiratory Tract InfectionsAnti-Bacterial AgentsFluoroquinolonesMoxifloxacinmoxifloxacinpharmacokineticsrespiratory tract infection

Identifiers

PMID26660898
PMCPMC5933663
OpenAlexW2266377908

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.