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Evaluating Ubrogepant-related adverse events using the FDA adverse event reporting system.
Author: CaoBing, ChenHang, GuShanshan, ShenYiming, ShenZhisen, ZhangYuna
Original Abstract of the Article :
Migraine has a high prevalence in the population and accounts for 12% of primary headaches. Ubrogepant is used for the treatment of acute migraine, and although some clinical trials have demonstrated the safety of Ubrogepant, its long-term safety in a large sample of the population remains to be inv...See full text at original site
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引用元:
https://doi.org/10.1080/14740338.2023.2251390
データ提供:米国国立医学図書館(NLM)
Ubrogepant: Evaluating Safety Through the FDA Adverse Event Reporting System
Ubrogepant, a medication used for the treatment of acute migraine, has shown promising results in clinical trials. However, the long-term safety of Ubrogepant in a larger population remains an area of ongoing investigation. This research utilizes the FDA Adverse Event Reporting System (FAERS) to assess the potential adverse events associated with Ubrogepant use. The study analyzes a large database of adverse event reports to identify potential safety concerns associated with this migraine medication.
Ubrogepant Safety: A Comprehensive Assessment
The study examines the safety profile of Ubrogepant through the FAERS database, providing valuable insights into potential adverse events. While the analysis reveals that Ubrogepant appears to be generally safe, the study emphasizes the importance of continued monitoring and further research to fully understand the long-term safety profile of this medication. The findings highlight the importance of ongoing pharmacovigilance to ensure the safety of medications used for migraine treatment.
Ensuring Medication Safety: A Continuous Process
This research emphasizes the importance of ongoing pharmacovigilance to ensure the safety of medications used for migraine treatment. The study utilizes the FAERS database to assess the potential adverse events associated with Ubrogepant, providing valuable insights into the safety profile of this medication. The findings underscore the need for continued monitoring and further research to fully understand the long-term safety of Ubrogepant in a larger population.
Dr. Camel's Conclusion
Just as a camel navigates the vast desert, seeking safe passage through treacherous terrain, we must navigate the complex world of medication safety. This research utilizes the FDA Adverse Event Reporting System to assess the potential safety of Ubrogepant, highlighting the importance of ongoing pharmacovigilance to ensure the well-being of migraine patients.
Date :
- Date Completed n.d.
- Date Revised 2023-08-24
Further Info :
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