Evidence map›Paper›PMID 42023114›Full record

ArticleFrontiers in medicine2026

Biologics and biosimilars medication errors in Saudi Arabia: a nationwide retrospective observational real-world study.

Nouf T Alshammri, Wafa S Alluwaymi, Ghadah A Assiri, Thamir M Alshammari

Abstract read
In one paragraph

Article in Frontiers in medicine, 2026. 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
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  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

4 authors.

Nouf T AlshammriTherapeutic Affairs Deputyship, Ministry of Health, Riyadh, Saudi Arabia.
Wafa S AlluwaymiTherapeutic Affairs Deputyship, Ministry of Health, Riyadh, Saudi Arabia.
Ghadah A AssiriDepartment of Clinical Pharmacy, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.
Thamir M AlshammariDepartment of Pharmacy Practice, College of Pharmacy, Jazan University, Jazan, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: In Saudi Arabia, the Ministry of Health reported 71, 332 errors from 2018 to 2019. Biologics and biosimilars are safe treatment options for various medical conditions; however, safety concerns remain. Immunogenicity and unique brand names can cause adverse reactions, and the ability to predict immune responses is limited. This study aims to determine the number and characteristics of medication errors associated with biological and biosimilar medications in Saudi Arabia from 2020 to 2023. Methods: A retrospective observational real-world study was conducted to analyze the number of biologic and biosimilar medication errors reported to the MOH, Saudi Arabia, from 2020 to 2023 using an electronic database as a data source. Categorical data were summarized as frequency and percentage. All analyses were performed using Microsoft Excel. Results: A total of 63,817 medication error reports related to biologics and biosimilars were identified. The majority occurred during the prescribing phase (76-79%) and were classified as non-harmful (Category B, ≈70%). Pharmacists were the leading reporters (87%), underlining their central role in patient safety. Adults (>18 years) represented the most affected demographic group (≈70%). Insulin and anticoagulants (enoxaparin and heparin) together accounted for the highest proportion of errors, highlighting these agents as key targets for safety interventions. Conclusion: This study offers a comprehensive national evaluation of medication errors associated with biologic and biosimilar products reported to the Saudi Ministry of Health between 2020 and 2023. High-alert medications, particularly insulin and anticoagulants, consistently ranked among the top error-related agents, highlighting the need for targeted interventions.

Indexed as

biologicalsbiosimilarshealthcare professionalsmedication errorpharmacovigilanceSaudi Arabia

Identifiers

PMID42023114
PMCPMC13096075

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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.