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The Association between PDE5 Inhibitors and Aneurysm/Arterial Dissection: A Pharmacovigilance Study Using WHO Safety Database.

Authors :
Koji Miyata
Yuki Izawa-Ishizawa
Takahiro Niimura
Hirofumi Hamano
Fuka Aizawa
Kenta Yagi
Kei Kawada
Yoshito Zamami
Mitsuhiro Goda
Keisuke Ishizawa
Source :
Journal of Medical Investigation; 2024, Vol. 71 Issue 1/2, p134-140, 7p
Publication Year :
2024

Abstract

Aneurysm and arterial dissection have been reported as adverse drug events, associated with angiogenesis inhibitors and fluoroquinolones. Specifically, several cases of severe arterial disease following cGMP-specific phosphodiesterase type 5 (PDE5) inhibitors usage have recently been reported. It is necessary to ascertain the risks of serious adverse events caused by PDE5 inhibitors. We aimed to evaluate the association of aneurysm and artery dissection with PDE5 inhibitors using VigiBase, which is a World Health Organization database of spontaneously reported adverse events, for explorative hypothesis-generating analysis. We performed disproportionality analysis using a dataset from inception in 1967 to December 2022 and calculated reporting odds ratios (ROR) between PDE5 inhibitors and arterial diseases. We extracted 195,839 reports on PDE5 inhibitors with 254 reports of arterial disease as adverse events from VigiBase. Disproportionality analysis showed disproportional signals for PDE5 inhibitors (ROR, 2.30; 95% confidence intervals, 2.04-2.61); disproportional signals were detected in analyses restricting the lesion site to the aorta or cerebral arteries. From stratified analysis, disproportional signals were noted in females, as well as males, generally recognized as a risk factor for artery diseases. This real-world data analysis suggests that PDE5 inhibitors may play a role in the development of lethal arterial disease. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13431420
Volume :
71
Issue :
1/2
Database :
Complementary Index
Journal :
Journal of Medical Investigation
Publication Type :
Academic Journal
Accession number :
181001509
Full Text :
https://doi.org/10.2152/jmi.71.134