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Safety of BRAF+MEK Inhibitor Combinations: Severe Adverse Event Evaluation.
タグ:
FAERS
2020/6/26
Serious adverse events with tocilizumab: Pharmacovigilance as an aid to prioritize monitoring in COVID-19.
タグ:
FAERS
2020/7/9
Facial Paralysis Following Influenza Vaccination: A Disproportionality Analysis Using the Vaccine Adverse Event Reporting System Database.
タグ:
VAERS
2020/7/23
A real-world disproportionality analysis of FDA Adverse Event Reporting System (FAERS) events for baricitinib.
タグ:
FAERS
2020/7/23
Ovary and uterus related adverse events associated with statin use: an analysis of the FDA Adverse Event Reporting System.
タグ:
FAERS
2020/7/21
Differences in safety profiles of newly approved medications for multiple myeloma in real-world settings versus randomized controlled trials.
タグ:
FAERS
2020/7/21
Indications and postoperative outcomes of surgery for laryngotracheal stenosis: A descriptive study.
タグ:
DPC
2020/7/20
A descriptive analysis of medicines safety advisories issued by national medicines regulators in Australia, Canada, the United Kingdom and the United States – 2007 to 2016.
タグ:
Pharmacoepidemiology
2020/07/23
Using Data from the Canadian Post-marketing Spontaneous Pharmacovigilance System for Drug Safety Research: A Feasibility Study.
タグ:
CVAR
2020/7/17
Using Data from the Canadian Post-marketing Spontaneous Pharmacovigilance System for Drug Safety Research: A Feasibility Study.
タグ:
CVAR
2020/7/17
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