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

Drug Injury Quarter

Person who experienced the adverse event (patient)

Event ID	CASEID	CASEVERSION	I F COD	EVENT DT	MFR DT	INIT FDA DT	FDA DT	REPT COD	AUTH NUM	MFR NUM	MFR SNDR	LIT REF	AGE	AGE COD	AGE GRP	GNDR COD	E SUB	WT	WT COD	REPT DT	TO MFR	OCCP COD	REPORTER COUNTRY	OCCR COUNTRY
127557301	12755730	1	I	20100205	20110330	20160916	20160916	EXP		US-ASTRAZENECA-2016SE98517	ASTRAZENECA		12.13	MON		M	Y	0.00000		20160916		MD	DE	DE

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	DOSE VBM	LOT NUM	DOSE FORM
127557301	12755730	1	PS	SYNAGIS	PALIVIZUMAB	1	Intramuscular	89 MG	UNKNOWN	INJECTION
127557301	12755730	2	SS	SYNAGIS	PALIVIZUMAB	1	Intramuscular	89 MG	UNKNOWN	INJECTION
127557301	12755730	3	SS	SYNAGIS	PALIVIZUMAB	1	Intramuscular	89 MG	UNKNOWN	INJECTION
127557301	12755730	4	SS	SYNAGIS	PALIVIZUMAB	1	Intramuscular	89 MG	UNKNOWN	INJECTION

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
127557301	12755730	1	Neuromyopathy
127557301	12755730	2	Neuromyopathy
127557301	12755730	3	Neuromyopathy
127557301	12755730	4	Neuromyopathy

Outcome of event

Event ID	CASEID	OUTC COD
127557301	12755730	HO

Reactions reported

Event ID	CASEID	DRUG REC ACT	PT
127557301	12755730		Pneumonia

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

no results found

Therapies reported

Event ID	CASEID	DSG DRUG SEQ	START DT	END DT
127557301	12755730	1	20091027	20091027
127557301	12755730	2	20091125	20091125
127557301	12755730	3	20091223	20091223
127557301	12755730	4	20100120	20100120