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Disproportionality Analysis of Safety with Nafcillin and Oxacillin with the FDA Adverse Event Reporting System (FAERS).
タグ:
FAERS
2019/12/18
Adverse Events Due to Insomnia Drugs Reported in a Regulatory Database and Online Patient Reviews: Comparative Study.
タグ:
FAERS
2019/11/9
Opioids and frequency counts in the US Food and Drug Administration Adverse Event Reporting System (FAERS) database: a quantitative view of the epidemic.
タグ:
FAERS
2019/11/7
Endocrine toxicity of immune checkpoint inhibitors: a real-world study leveraging US Food and Drug Administration adverse events reporting system.
タグ:
FAERS
2019/11/7
Comparing Acute Kidney Injury Reports Among Antibiotics: A Pharmacovigilance Study of the FDA Adverse Event Reporting System (FAERS).
タグ:
FAERS
2019/11/7
Ischemic and Thrombotic Events Associated with Concomitant Xa-inhibiting Direct Oral Anticoagulants and Antiepileptic Drugs: Analysis of the FDA Adverse Event Reporting System (FAERS).
タグ:
FAERS
2019/11/7
Evaluation of the Expression Time of Ganciclovir-Induced Adverse Events Using JADER and FAERS.
タグ:
FAERS
JADER
2019/11/7
Proton-pump inhibitor use is associated with a broad spectrum of neurological adverse events including impaired hearing, vision, and memory.
タグ:
FAERS
2019/11/23
Safety of the 9-Valent Human Papillomavirus Vaccine.
タグ:
FAERS
VAERS
2019/11/20
Rhabdomyolysis Associations with Antibiotics: A Pharmacovigilance Study of the FDA Adverse Event Reporting System (FAERS).
タグ:
FAERS
2019/11/2
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