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Exploring the Cardiovascular Safety Profile of Ibuprofen: Insights from EudraVigilance Database
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Background: Ibuprofen is one of the most accessible non-steroidal anti-inflammatory drugs (NSADs), exhibiting non-selective reversible inhibition on COX-1 and COX-2. A series of common adverse reactions have been mentioned through the years: gastrointestinal (gastritis, ulceration, hemorrhage, or perforation), renal, hematologic, and cardiovascular. Objective: The aim of this study was to assess the real-world impact of ibuprofen regarding cardiovascular safety, utilizing an established pharmacovigilance database. Methods: Descriptive and disproportionality-based methods were used. Forty specific descriptors of cardiovascular effects were selected. Eight other NSADs and the combination of ibuprofen and pseudoephedrine were used as comparators. Results: A total of 58,760 cases were identified as being associated with ibuprofen in EudraVigilance. Stroke was reported for ibuprofen with a lower probability compared with etoricoxib (ROR: 0.34; 95% CI: 0.21–0.55), celecoxib (ROR: 0.07; 95% CI: 0.06–0.10), meloxicam (ROR: 0.25; 95% CI: 0.14–0.43), acetylsalicylic acid (ROR: 0.07; 95% CI: 0.05–0.09), and ibuprofen/pseudoephedrine (ROR: 0.11; 95% CI: 0.05–0.25). Thrombosis was reported for ibuprofen with a higher probability only relative to ketoprofen (ROR: 2.95; 95% CI: 1.71–5.09). Hypertension was reported for ibuprofen as being more probable than for acetylsalicylic acid (ROR: 1.58; 95% CI: 1.43–1.76). Myocardial infarction was reported as being more probable for ibuprofen than ketoprofen (ROR: 2.31; 95% CI: 1.57–3.40) or nimesulide (ROR: 2.43; 95% CI: 1.25–4.73). Conclusions: Overall, according to our study, the probability of reported cardiovascular adverse reactions is lower than those determined for the rest of the NSAIDs; however, taking into consideration the inherent limitations of the study, further clinical investigations would contribute to a better understanding of the cardiovascular safety of ibuprofen.
Title: Exploring the Cardiovascular Safety Profile of Ibuprofen: Insights from EudraVigilance Database
Description:
Background: Ibuprofen is one of the most accessible non-steroidal anti-inflammatory drugs (NSADs), exhibiting non-selective reversible inhibition on COX-1 and COX-2.
A series of common adverse reactions have been mentioned through the years: gastrointestinal (gastritis, ulceration, hemorrhage, or perforation), renal, hematologic, and cardiovascular.
Objective: The aim of this study was to assess the real-world impact of ibuprofen regarding cardiovascular safety, utilizing an established pharmacovigilance database.
Methods: Descriptive and disproportionality-based methods were used.
Forty specific descriptors of cardiovascular effects were selected.
Eight other NSADs and the combination of ibuprofen and pseudoephedrine were used as comparators.
Results: A total of 58,760 cases were identified as being associated with ibuprofen in EudraVigilance.
Stroke was reported for ibuprofen with a lower probability compared with etoricoxib (ROR: 0.
34; 95% CI: 0.
21–0.
55), celecoxib (ROR: 0.
07; 95% CI: 0.
06–0.
10), meloxicam (ROR: 0.
25; 95% CI: 0.
14–0.
43), acetylsalicylic acid (ROR: 0.
07; 95% CI: 0.
05–0.
09), and ibuprofen/pseudoephedrine (ROR: 0.
11; 95% CI: 0.
05–0.
25).
Thrombosis was reported for ibuprofen with a higher probability only relative to ketoprofen (ROR: 2.
95; 95% CI: 1.
71–5.
09).
Hypertension was reported for ibuprofen as being more probable than for acetylsalicylic acid (ROR: 1.
58; 95% CI: 1.
43–1.
76).
Myocardial infarction was reported as being more probable for ibuprofen than ketoprofen (ROR: 2.
31; 95% CI: 1.
57–3.
40) or nimesulide (ROR: 2.
43; 95% CI: 1.
25–4.
73).
Conclusions: Overall, according to our study, the probability of reported cardiovascular adverse reactions is lower than those determined for the rest of the NSAIDs; however, taking into consideration the inherent limitations of the study, further clinical investigations would contribute to a better understanding of the cardiovascular safety of ibuprofen.
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