# A disproportionality analysis of FDA adverse event reporting system (FAERS) events for methimazole and propylthiouracil

**Authors:** Yun Li, Hang Li, Qiong Sun, Qin Long, Vijayalakshmi Kakulapati, Vijayalakshmi Kakulapati, Vijayalakshmi Kakulapati

PMC · DOI: 10.1371/journal.pone.0328889 · PLOS One · 2025-08-14

## TL;DR

This study analyzes adverse events linked to methimazole and propylthiouracil using FDA safety data to improve their safe clinical use.

## Contribution

The study provides a detailed safety profile of methimazole and propylthiouracil using FAERS data from 2004 to 2023.

## Key findings

- Methimazole was associated with 8 adverse event categories reported ≥30 times.
- Propylthiouracil had 12 adverse event categories reported ≥10 times.
- Adverse events for methimazole occurred faster (median 31 days) than for propylthiouracil (median 90 days).

## Abstract

Methimazole and propylthiouracil are the most common antithyroid drugs. We assessed the safety signals associated with methimazole and propylthiouracil by data mining the FDA pharmacovigilance database.

Data were retrieved from the FAERS database from the 1st quarter of 2004 through the 4th quarter of 2023. A disproportionate analysis of reporting advantage ratios was used to assess potential associations between adverse events and methimazole/propylthiouracil.

A total of 17,379,609 reports were extracted, of which 5,317 cases of methimazole and 1,761 cases of propylthiouracil were classified as primary suspect reports. After combining the same primary ID, 1586 patients with methimazole and 446 patients with propylthiouracil were retained. We observed 8 categories of SOCs with a reported number ≥ 30 for methimazole and 12 categories of SOCs with a reported number ≥ 10 for propylthiouracil. The median time to adverse events in patients with methimazole was 31 days, with an interquartile range of 31–74 days. The median time to adverse events in patients with propylthiouracil was 90 days, with an interquartile range was 20–388.5 days.

Our study provided a more in-depth and extensive understanding of adverse events that may be associated with methimazole and propylthiouracil, which will help to reduce the risk of adverse events in the clinical treatment of methimazole and propylthiouracil.

## Linked entities

- **Chemicals:** methimazole (PubChem CID 1349907), propylthiouracil (PubChem CID 657298)

## Full-text entities

- **Genes:** TPO (thyroid peroxidase) [NCBI Gene 7173] {aka MSA, TDH2A, TPX}, CYP19A1 (cytochrome P450 family 19 subfamily A member 1) [NCBI Gene 1588] {aka ARO, ARO1, CPV1, CYAR, CYP19, CYPXIX}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}, TG (thyroglobulin) [NCBI Gene 7038] {aka AITD3, TGN}, LINC-ROR (long intergenic non-protein coding RNA, regulator of reprogramming) [NCBI Gene 100885779] {aka ROR, lincRNA-RoR, lincRNA-ST8SIA3}
- **Diseases:** respiratory, thoracic and mediastinal disorder (MESH:D008480), cancers of the (MESH:D009369), hepatic encephalopathy (MESH:D006501), acute hepatic failure (MESH:D017114), , familial (MESH:D000073376), Thyroiditis (MESH:D013966), Hepatobiliary disorders (MESH:D004066), systemic, small-vessel vasculitis (MESH:C565222), PTU (OMIM:171200), thyroid disease (MESH:D013959), AEs (MESH:D064420), jaundice (MESH:D007565), haemorrhage (MESH:D006470), multiple organ dysfunction syndrome (MESH:D009102), pleural effusion (MESH:D010996), musculoskeletal and connective tissue disorders (MESH:D003240), polyarthritis (MESH:D001168), ORCID iD (MESH:C535742), damage (MESH:D020263), poisoning (MESH:D011041), PT (MESH:D006526), injury (MESH:D014947), Vitreoretinal Traction Syndrome (MESH:D058499), respiratory failure (MESH:D012131), immune system (MESH:D007154), oropharyngeal pain (MESH:D009959), Agranulocytosis (MESH:D000380), disorders (MESH:D009358), ATDs (MESH:D000081015), endocrine disorders (MESH:D004700), systemic diseases (MESH:D034721), AAV (MESH:D014657), blood and lymphatic system disorders (MESH:D006425), acute pancreatitis (MESH:D010195), ANCA-associated vasculitis (MESH:D056648), hyperthyroidism (MESH:D006980), congenital, familial and genetic disorders (MESH:D030342), dysmorphism (MESH:D057215), premature baby (MESH:C536271), gastrointestinal distress (MESH:D012128), Graves' disease (MESH:D006111), diarrhea (MESH:D003967), gastrointestinal disorders (MESH:D005767), system (MESH:D015619), rhabdomyolysis (MESH:D012206), Cutaneous vasculitis (MESH:D018366), FAERS (MESH:D002318), hepatic failure (MESH:D017093), goitre (MESH:D006042), cholestasis (MESH:D002779), fever (MESH:D005334), Thyrotoxicosis (MESH:C566386), angioedema (MESH:D000799), ear and labyrinth disorders (MESH:D007762), nervous system disorders (MESH:D009422), digestive system cancers (MESH:D004067), toxic nodular goiter (MESH:D006044), vascular disorders (MESH:D002561), death (MESH:D003643), pruritus (MESH:D011537)
- **Chemicals:** acetylsalicylic acid (MESH:D001241), Everolimus (MESH:D000068338), sildenafil (MESH:D000068677), vinorelbine (MESH:D000077235), vinca alkaloids (MESH:D014748), -D-24- (-), Anastrozole (MESH:D000077384), tyrosine (MESH:D014443), SOC (MESH:C001599), Methimazole (MESH:D008713), PTU (MESH:D011441), Vincristine (MESH:D014750), iodine (MESH:D007455), topotecan (MESH:D019772)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** -D-24-51574A — Homo sapiens (Human), Melanoma, Cancer cell line (CVCL_W871)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12352670/full.md

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12352670/full.md

## References

47 references — full list in the complete paper: https://tomesphere.com/paper/PMC12352670/full.md

---
Source: https://tomesphere.com/paper/PMC12352670