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
127767391	12776739	1	I		20100203	20160923	20160923	EXP		US-ASTRAZENECA-2016SF01000	ASTRAZENECA		0.00			F	Y	0.00000		20160923		MD	DE	DE

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	DECHAL	RECHAL	LOT NUM	DOSE AMT	DOSE UNIT	DOSE FORM
127767391	12776739	1	PS	SYNAGIS	PALIVIZUMAB	1	Intramuscular	U	U	UNKNOWN	87	MG	INJECTION
127767391	12776739	2	SS	SYNAGIS	PALIVIZUMAB	1	Intramuscular	U	U	UNKNOWN	91	MG	INJECTION
127767391	12776739	3	SS	SYNAGIS	PALIVIZUMAB	1	Intramuscular	U	U	UNKNOWN	95	MG	INJECTION

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
127767391	12776739	1	Antiviral prophylaxis
127767391	12776739	2	Antiviral prophylaxis
127767391	12776739	3	Antiviral prophylaxis

Outcome of event

Event ID	CASEID	OUTC COD
127767391	12776739	HO

Reactions reported

Event ID	CASEID	DRUG REC ACT	PT
127767391	12776739		Gastroenteritis
127767391	12776739		Nosocomial infection

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
127767391	12776739	1	20081009	20081009
127767391	12776739	2	20081108	20081108
127767391	12776739	3	20090204	20090204