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Post-licensure surveillance of 13-valent pneumococcal conjugate vaccine (PCV13) in adults aged ⩾19years old in the United States, Vaccine Adverse Event Reporting System (VAERS), June 1, 2012-December 31, 2015.
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VAERS
FAERS
2016/11/12
Exploiting heterogeneous publicly available data sources for drug safety surveillance: computational framework and case studies.
タグ:
FAERS
2016/11/5
A remarkable case of rhabdomyolysis associated with ingestion of energy drink ‘neon volt’.
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FAERS
2016/11/3
Clinical characteristics of adverse events associated with therapeutic monoclonal antibodies in Korea.
タグ:
KAERS
FAERS
2016/11/3
Carboplatin-induced hematotoxicity among patients with non-small cell lung cancer: Analysis on clinical adverse events and drug-gene interactions.
タグ:
FAERS
2016/11/02
Tocilizumab-induced pancreatitis: case report and review of data from the FDA Adverse Event Reporting System.
タグ:
FAERS
2016/10/28
Is GERD a Factor in Osteonecrosis of the Jaw? Evidence of Pathology Linked to G6PD Deficiency and Sulfomucins.
タグ:
FAERS
2016/10/25
Seasonal and Geographic Variation in Adverse Event Reporting.
タグ:
FAERS
2016/10/18
Chemical Leukoderma Associated with Methylphenidate Transdermal System: Data From the US Food and Drug Administration Adverse Event Reporting System.
タグ:
FAERS
2016/10/18
Differences in reproductive toxicology between alopecia drugs: an analysis on adverse events among female and male cases.
タグ:
FAERS
2016/10/16
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