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An investigation into drug products withdrawn from the EU market between 2002 and 2011 for safety reasons and the evidence used to support the decision-making.
タグ:
EudraVigilance
2014/1/18
Traceability of biopharmaceuticals in spontaneous reporting systems: a cross-sectional study in the FDA Adverse Event Reporting System (FAERS) and EudraVigilance databases.
タグ:
FAERS
EudraVigilance
2013/6/19
Adverse drug reactions reported by consumers for nervous system medications in Europe 2007 to 2011.
タグ:
EudraVigilance
2013/6/15
Choosing thresholds for statistical signal detection with the proportional reporting ratio.
タグ:
EudraVigilance
2013/6/12
Side effects reported by European consumers for medications for erectile dysfunction.
タグ:
EudraVigilance
2013/4/1
Adverse drug reactions in children reported by European consumers from 2007 to 2011.
タグ:
EudraVigilance
2013/11/6
Assessing the extent and impact of the masking effect of disproportionality analyses on two spontaneous reporting systems databases.
タグ:
EudraVigilance
2013/11/19
Acute disseminated encephalomyelitis onset: evaluation based on vaccine adverse events reporting systems.
タグ:
EudraVigilance
VAERS
2013/10/23
Side effects of antineoplastic and immunomodulating medications reported by European consumers.
タグ:
EudraVigilance
2013/1/1
Are non-serious adverse reactions to psychiatric drugs really non-serious?
タグ:
EudraVigilance
2013/08/21
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