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Safety of Biologics Approved for the Treatment of Rheumatoid Arthritis and Other Autoimmune Diseases: A Disproportionality Analysis from the FDA Adverse Event Reporting System (FAERS).
タグ:
FAERS
2018/6/7
Generation of an annotated reference standard for vaccine adverse event reports.
タグ:
VAERS
2018/6/9
Psoriasis and the risk of foot and ankle tendinopathy or enthesopathy in the absence of psoriatic arthritis: a population-based study.
タグ:
THIN
2018/6/5
Burden of herpes zoster in 16 selected immunocompromised populations in England: a cohort study in the Clinical Practice Research Datalink 2000-2012.
タグ:
CPRD
2018/6/9
Skin Hypersensitivity to Oral Budesonide: Case Report and Review of the FDA Adverse Event Reporting System Database.
タグ:
FAERS
2018/6/3
Safety Surveillance of Diphtheria and Tetanus Toxoids and Acellular Pertussis (DTaP) Vaccines.
タグ:
VAERS
2018/6/6
Drug-Associated Acute Kidney Injury Identified in the United States Food and Drug Administration Adverse Event Reporting System Database.
タグ:
FAERS
2018/6/9
An Information Enhanced Framework for Reporting Medication Events.
タグ:
FAERS
2018/6/3
Thirteen-year trend in the persistence with vitamin K antagonists for venous thromboembolism in the UK: a cohort study.
タグ:
CPRD
2018/5/26
Adverse events of smoking cessation treatments (nicotine replacement therapy and non-nicotine prescription medication) and electronic cigarettes in the Food and Drug Administration Adverse Event Reporting System, 2004-2016.
タグ:
FAERS
2018/5/31
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