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
127297121	12729712	1	I	20160821	20160905	20160909	20160909	EXP		PHHY2016IT123647	NOVARTIS		30.63	YR		M	Y	80.00000	KG	20160909		OT	IT	IT

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	DOSE VBM	NDA NUM	DOSE AMT	DOSE UNIT
127297121	12729712	1	PS	VOLTAREN	DICLOFENAC SODIUM	1	Intramuscular	75 MG, TOTAL	19201	75	MG
127297121	12729712	2	SS	BACTRIM	SULFAMETHOXAZOLETRIMETHOPRIM	1	Oral	160 MG, TOTAL	0	160	MG
127297121	12729712	3	SS	TACHIPIRINA	ACETAMINOPHEN	1	Oral	1000 MG, TOTAL	0	1000	MG

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
127297121	12729712	1	Back pain
127297121	12729712	2	Meningitis
127297121	12729712	3	Pyrexia

Outcome of event

Event ID	CASEID	OUTC COD
127297121	12729712	HO

Reactions reported

Event ID	CASEID	PT
127297121	12729712	Epistaxis
127297121	12729712	Gingival bleeding
127297121	12729712	Petechiae
127297121	12729712	Thrombocytopenia

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
127297121	12729712	1	20160820	20160820
127297121	12729712	2	20160820	20160820
127297121	12729712	3	20160820	20160820