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Systematic analysis of the adverse effects of commonly used clinical tetracycline drugs based on the FAERS database.
タグ:
FAERS
2024/8/14
Cardiovascular toxicities of selective ret-specific tyrosine kinase inhibitors: a pharmacovigilance study based on the United States Food and Drug Administration Adverse Event Reporting System database.
タグ:
FAERS
2024/8/14
Amiodarone-Induced Anaphylaxis.
タグ:
FAERS
2024/8/13
Ocular adverse events associated with platins: a disproportionality analysis of pharmacovigilance data and extensive systematic review of case reports.
タグ:
FAERS
2024/8/13
Real-world study of adverse events associated with gepant use in migraine treatment based on the VigiAccess and U.S. Food and Drug Administration’s adverse event reporting system databases.
タグ:
FAERS
2024/8/15
Safety assessment of neurokinin-1 receptor antagonist: real-world adverse event analysis from the FAERS database.
タグ:
FAERS
2024/8/15
A Biologic With Otologic Consequences: Analysis of Hearing Loss and Teprotumumab Using the FDA Adverse Event Reporting System.
タグ:
FAERS
2024/8/15
Adverse events associated with teriparatide: a real-world disproportionality analysis of the FDA adverse event reporting system (FAERS).
タグ:
FAERS
2024/8/14
The real-world safety profile of tirzepatide: pharmacovigilance analysis of the FDA Adverse Event Reporting System (FAERS) database.
タグ:
FAERS
2024/8/14
Pharmacovigilance analysis of orlistat adverse events based on the FDA adverse event reporting system (FAERS) database.
タグ:
FAERS
2024/8/16
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