Evidence map›Paper›PMID 28117319›Full record

ArticleScientia pharmaceutica2016

Investigation of the Bioequivalence of Rosuvastatin 20 mg Tablets after a Single Oral Administration in Mediterranean Arabs Using a Validated LC-MS/MS Method.

Abdel Naser Zaid, Rowa Al Ramahi, Rita Cortesi, Ayman Mousa, Nidal Jaradat, Nadia Ghazal, Rana Bustami

Open access · goldAbstract read
In one paragraph

Article in Scientia pharmaceutica, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 26% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
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 2 institutions in 2 countries.

Abdel Naser ZaidDepartment of Pharmacy, Faculty of Medicine & health Sciences, An-Najah National University, 44859 Nablus, P.O. Box 7, Palestine. anzaid@najah.edu.
Rowa Al RamahiDepartment of Pharmacy, Faculty of Medicine & health Sciences, An-Najah National University, 44859 Nablus, P.O. Box 7, Palestine. rawa_ramahi@najah.edu.
Rita CortesiDepartment of Life Sciences and Biotechnology, University of Ferrara, 44121 Ferrara, Italy. crt@unife.it.
Ayman MousaR&D department Avalon Pharma (Middle East Pharmaceutical Industries Co. Ltd), 11372 Riyadh, Kingdom of Saudi Arabia. ayman@avalon.com.sa.
Nidal JaradatDepartment of Pharmacy, Faculty of Medicine & health Sciences, An-Najah National University, 44859 Nablus, P.O. Box 7, Palestine. nidaljaradat@najah.edu.
Nadia GhazalNaratech Pharma Consultancy, 11814 Amman, Jordan. nadia@naratech.net.
Rana BustamiPharmaceutical Research Unit, Complex No 19, Yajouz St 19, 11910 Amman, Jordan. rtbustami@pru.com.jo.
An-Najah National University · PSUniversity of Ferrara · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is a wide inter-individual response to statin therapy including rosuvastatin calcium (RC), and it has been hypothesized that genetic differences may contribute to these variations. In fact, several studies have shown that pharmacokinetic (PK) parameters for RC are affected by race. The aim of this study is to demonstrate the interchangeability between two generic RC 20 mg film-coated tablets under fasting conditions among Mediterranean Arabs and to compare the pharmacokinetic results with Asian and Caucasian subjects from other studies. A single oral RC 20 mg dose, randomized, open-label, two-way crossover design study was conducted in 30 healthy Mediterranean Arab volunteers. Blood samples were collected prior to dosing and over a 72-h period. Concentrations in plasma were quantified using a validated liquid chromatography tandem mass spectrometry method. Twenty-six volunteers completed the study. Statistical comparison of the main PK parameters showed no significant difference between the generic and branded products. The point estimates (ratios of geometric mean %) were 107.73 (96.57-120.17), 103.61 (94.03-114.16), and 104.23 (94.84-114.54) for peak plasma concentration (C

Indexed as

bioequivalenceefficacyin vitro releaserosuvastatin calciumsafety

Identifiers

PMID28117319
PMCPMC5064244
OpenAlexW2529208837

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.