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Subgroup disproportionality analysis of dementia-related adverse events with sacubitril/valsartan across geographical regions.
タグ:
KAERS
FAERS
2024/9/4
Drugs Associated with Urinary Retention Adverse Reactions: A Joint Analysis of FDA Adverse Event Reporting System and Mendelian Randomization.
タグ:
FAERS
2024/9/3
Comparative analysis of adverse event risks in breast cancer patients receiving pembrolizumab combined with paclitaxel versus paclitaxel monotherapy: insights from the FAERS database.
タグ:
FAERS
2024/9/5
CAR-T therapy pulmonary adverse event profile: a pharmacovigilance study based on FAERS database (2017-2023).
タグ:
FAERS
2024/9/5
Ocular adverse events associated with antibody-drug conjugates in oncology: a pharmacovigilance study based on FDA adverse event reporting system (FAERS).
タグ:
FAERS
2024/9/4
Adverse events associated with Atogepant: a FAERS-based pharmacovigilance analysis.
タグ:
FAERS
2024/9/7
Syncope after live attenuated influenza vaccine: Reports to the Vaccine Adverse Event Reporting System (2003-2024).
タグ:
VAERS
FAERS
2024/9/7
Analysis of publicly available adverse events reported for pediatric patients treated with Janus kinase inhibitors.
タグ:
CVAR
FAERS
2024/9/5
A real-world disproportionality analysis of baloxavir marboxil: post-marketing pharmacovigilance data.
タグ:
FAERS
2024/9/5
Therapeutic failure reported with HIV long-acting injectables: An analysis of the FDA Adverse Event Reporting System from 2021 to 2024.
タグ:
FAERS
2024/9/5
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