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Testing the technology acceptance model for evaluating healthcare professionals’ intention to use an adverse event reporting system.
タグ:
FAERS
2008/01/29
Rotavirus live, oral, pentavalent vaccine.
タグ:
VAERS
2008/1/19
Inactivated influenza vaccine (IIV) in children <2 years of age: examination of selected adverse events reported to the Vaccine Adverse Event Reporting System (VAERS) after thimerosal-free or thimerosal-containing vaccine.
タグ:
VAERS
2007/12/21
Rhabdomyolysis reports show interaction between simvastatin and CYP3A4 inhibitors.
タグ:
FAERS
2009/2/12
Hallucinations and other psychotic symptoms associated with the use of attention-deficit/hyperactivity disorder drugs in children.
タグ:
FAERS
2009/01/28
Cardiac and noncardiac fibrotic reactions caused by ergot-and nonergot-derived dopamine agonists.
タグ:
FAERS
2009/01/27
Human papillomavirus vaccine safety in pediatric patients: an evaluation of the Vaccine Adverse Event Reporting System.
タグ:
VAERS
2009/1/22
Babesia infection through blood transfusions: reports received by the US Food and Drug Administration, 1997-2007.
タグ:
FAERS
2008/11/28
Intracranial hemorrhage and liver-associated deaths associated with tipranavir/ritonavir: review of cases from the FDA’s Adverse Event Reporting System.
タグ:
FAERS
2008/11/26
Pediatric drug surveillance and the Food and Drug Administration’s adverse event reporting system: an overview of reports, 2003-2007.
タグ:
FAERS
2008/11/15
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