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Evaluation of the quality and value of data sources for postmarket surveillance of the safety of cough and cold medications in children.
タグ:
FAERS
2018/12/24
Use of Spontaneous Reporting Systems to Detect Host-Medication Interactions: Sex Differences in Oral Anti-Diabetic Drug-Associated Myocardial Infarction.
タグ:
FAERS
2018/12/21
Evaluation of pregabalin-induced adverse events related to falls using the FDA adverse event reporting system and Japanese Adverse Drug Event Report databases.
タグ:
FAERS
JADER
2018/12/21
Evaluation of Postmarketing Reports from Industry-Sponsored Programs in Drug Safety Surveillance.
タグ:
FAERS
2018/12/21
Analysis of tolerance to antidepressant drug treatment in FDA Adverse Event Reporting System.
タグ:
FAERS
2018/12/19
Reply to Dr. Gentili’ “Analysis of tolerance to antidepressant drugs in FDA Adverse Event Reporting System”.
タグ:
FAERS
2018/12/19
Pharmacovigilance evaluation of the relationship between impaired glucose metabolism and BCR-ABL inhibitor use by using an adverse drug event reporting database.
タグ:
FAERS
JADER
2018/12/19
Association of Noninfectious Pneumonia With Ustekinumab Use.
タグ:
FAERS
2018/12/13
Risk of malignant lymphoma in patients with rheumatoid arthritis treated with biological disease-modifying antirheumatic drugs and methotrexate.
タグ:
FAERS
JADER
CVAR
CVARD
2018/12/12
PathFX provides mechanistic insights into drug efficacy and safety for regulatory review and therapeutic development.
タグ:
FAERS
2018/12/12
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