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Liver injury associated with endothelin receptor antagonists: a pharmacovigilance study based on FDA adverse event reporting system data.
タグ:
FAERS
2024/6/21
Safety profile of lasmiditan: a retrospective post-marketing pharmacovigilance study based on the real-world data of FAERS database.
タグ:
FAERS
2024/6/20
Severe anaphylaxis after chimeric antigen receptor T-cell injection: a case report.
タグ:
FAERS
2024/6/19
Adverse events of direct factor Xa inhibitors: a disproportionality analysis of the FAERS database.
タグ:
FAERS
2024/6/18
Adverse events in different administration routes of semaglutide: a pharmacovigilance study based on the FDA adverse event reporting system.
タグ:
FAERS
2024/6/18
The association between ketamine and esketamine and suicidality: reports to the Food And Drug Administration Adverse Event Reporting System (FAERS).
タグ:
FAERS
2024/6/17
A retrospective pharmacovigilance study of post-marketing safety concerns with cefuroxime.
タグ:
FAERS
2024/6/17
Postmarketing Safety Concerns of Teprotumumab: A Real-World Pharmacovigilance Assessment.
タグ:
FAERS
2024/6/16
Relationship between Anaplastic Lymphoma Kinase Inhibitors and Epileptic Seizure Disorder: A Post-Marketing Surveillance Study.
タグ:
FAERS
2024/5/21
Adverse drug reactions in neonates: a brief analysis of the FDA adverse event reporting system.
タグ:
FAERS
2024/6/21
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