Post-marketing safety signal profile of mavacamten in the FDA adverse event reporting system (FAERS): a disproportionality analysis

Juan Wu, Chi Chen, Tao Zheng

Open source

DOI: 10.3389/fphar.2026.1906371
Published: 2026-09-09
Container: Frontiers in Pharmacology
Publisher: Frontiers Media SA
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.3389/fphar.2026.1906371,
  title = {Post-marketing safety signal profile of mavacamten in the FDA adverse event reporting system (FAERS): a disproportionality analysis},
  author = {Juan Wu and Chi Chen and Tao Zheng},
  year = {2026},
  journal = {Frontiers in Pharmacology},
  doi = {10.3389/fphar.2026.1906371},
  url = {https://doi.org/10.3389/fphar.2026.1906371}
}

RIS

TY  - JOUR
TI  - Post-marketing safety signal profile of mavacamten in the FDA adverse event reporting system (FAERS): a disproportionality analysis
AU  - Juan Wu
AU  - Chi Chen
AU  - Tao Zheng
PY  - 2026
JO  - Frontiers in Pharmacology
DO  - 10.3389/fphar.2026.1906371
UR  - https://doi.org/10.3389/fphar.2026.1906371
ER  -

APA

Wu, J., Chen, C., & Zheng, T. (2026). Post-marketing safety signal profile of mavacamten in the FDA adverse event reporting system (FAERS): a disproportionality analysis. Frontiers in Pharmacology. https://doi.org/10.3389/fphar.2026.1906371

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crossref · retrieved 2026-09-25T09:08:54.517Z