Evidence map›Paper›PMID 29063992›Full record

ReviewJournal of assisted reproduction and genetics2018

FDA-approved drugs that are spermatotoxic in animals and the utility of animal testing for human risk prediction.

Elizabeth R Rayburn, Liang Gao, Jiayi Ding, Hongxia Ding, Jun Shao, Haibo Li

Open access · greenAbstract readReview
In one paragraph

Review in Journal of assisted reproduction and genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 21% 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

4 citing papers in PubMed, 14 citations in OpenAlex.

  1. Ameliorative effects of vitamin C and garlic (Frontiers in veterinary science · 2025
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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

6 authors at 3 institutions in 1 country.

Elizabeth R RayburnCLIA Laboratory Director, Birmingham, AL, 35242, USA.
Liang GaoDepartment of Clinical Laboratory Sciences, Nantong Maternity and Child Health Hospital, Nantong, 226018, China.
Jiayi DingDepartment of Reproductive Medicine, Nantong Maternity and Child Health Hospital, Nantong, 226018, China.
Hongxia DingPharmacodia (Beijing) Co., Ltd, Beijing, 100085, China.
Jun ShaoDepartment of Reproductive Medicine, Nantong Maternity and Child Health Hospital, Nantong, 226018, China.
Haibo LiDepartment of Clinical Laboratory Sciences, Nantong Maternity and Child Health Hospital, Nantong, 226018, China. ntlihaibo2015@163.com.
Nantong Maternity and Child Health Hospital · CNAstellas Pharma (China) · CNNantong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThis study reviews FDA-approved drugs that negatively impact spermatozoa in animals, as well as how these findings reflect on observations in human male gametes.

methodsThe FDA drug warning labels included in the DailyMed database and the peer-reviewed literature in the PubMed database were searched for information to identify single-ingredient, FDA-approved prescription drugs with spermatotoxic effects.

resultsA total of 235 unique, single-ingredient, FDA-approved drugs reported to be spermatotoxic in animals were identified in the drug labels. Forty-nine of these had documented negative effects on humans in either the drug label or literature, while 31 had no effect or a positive impact on human sperm. For the other 155 drugs that were spermatotoxic in animals, no human data was available.

conclusionThe current animal models are not very effective for predicting human spermatotoxicity, and there is limited information available about the impact of many drugs on human spermatozoa. New approaches should be designed that more accurately reflect the findings in men, including more studies on human sperm in vitro and studies using other systems (ex vivo tissue culture, xenograft models, in silico studies, etc.). In addition, the present data is often incomplete or reported in a manner that prevents interpretation of their clinical relevance. Changes should be made to the requirements for pre-clinical testing, drug surveillance, and the warning labels of drugs to ensure that the potential risks to human fertility are clearly indicated.

Indexed as

AnimalsDrug ApprovalDrug LabelingHumansMalePubMedSpermatogenesisSpermatozoaToxicity TestsUnited StatesUnited States Food and Drug AdministrationDrug warning labelsInfertilityReproductive toxicologySpermatotoxicity

Identifiers

PMID29063992
PMCPMC5845034
OpenAlexW2767161839

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.