Abstract | AIM: METHODS: We performed a quantitative risk analysis of central nervous system (CNS) adverse events of rufinamide from all randomized, double-blind, add-on, placebo-controlled trials. The meta-analysis was undertaken with fixed effects models. RESULTS: Of the 886 publications reviewed, 99 papers were retrieved and five articles met the inclusion criteria. One thousand two hundred and fifty-two patients were included. Our study showed that exposure to rufinamide was associated with a significant increase in risk of somnolence [relative ratio (RR) 1.87; 95% confidence interval (CI) 1.33, 2.62; P = 0.0003], dizziness (RR 2.66; 95% CI 2.00, 3.55; P = 0.00001), fatigue (RR 2.14; 95% CI 1.57, 2.91; P = 0.01) and headache (RR 1.28; 95% CI 1.02, 1.59, P = 0.03). In addition, exposure to rufinamide was associated with higher treatment discontinuation rates as compared with placebo (RR 2.65; 95% CI 1.74, 4.03; P = 0.00001). CONCLUSIONS: The risk of CNS adverse events appears to be increased in patients exposed to rufinamide as well as the treatment discontinuation rates. However, although statistical associations were significant, additional long term safety studies are required to confirm the clinical significance of these findings, as most reports described only mild and moderate adverse events.
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Authors | Abdulaziz M S Alsaad, Gideon Koren |
Journal | British journal of clinical pharmacology
(Br J Clin Pharmacol)
Vol. 78
Issue 6
Pg. 1264-71
(Dec 2014)
ISSN: 1365-2125 [Electronic] England |
PMID | 25132372
(Publication Type: Journal Article, Meta-Analysis)
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Copyright | © 2014 The British Pharmacological Society. |
Chemical References |
- Anticonvulsants
- Triazoles
- rufinamide
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Topics |
- Anticonvulsants
(adverse effects)
- Central Nervous System Diseases
(chemically induced)
- Disorders of Excessive Somnolence
(chemically induced)
- Dizziness
(chemically induced)
- Drug Resistance
- Epilepsy
(drug therapy)
- Fatigue
(chemically induced)
- Headache
(chemically induced)
- Humans
- Randomized Controlled Trials as Topic
- Risk
- Triazoles
(adverse effects)
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