Safety Rates Drug Report: ARIXTRA Acute generalised exanthematous pustulosis adverse events in 2016 Q3 - FDA prescription drugs adverse events in an open, searchable, online, public database

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Drug Injury Quarter

Drug: ARIXTRA Injury: Acute generalised exanthematous pustulosis Quarter: 2016Q3

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Event ID	DRUGNAME	PT	Drug Manufacturer	Patient Age	Sex	Weight	Date (YYYYMMDD)	Country
127209752	ARIXTRA	Acute generalised exanthematous pustulosis	AVENTIS	87.00 YR	F	0	20160908	FR

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