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
127395212	12739521	2	F	201606	20160912	20160913	20160915	EXP		BR-JNJFOC-20160909295	JANSSEN		17.03	YR	T	M	Y	60.00000	KG	20160915		CN	BR	BR

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	DOSE VBM	CUM DOSE CHR	CUM DOSE UNIT	DECHAL	RECHAL	LOT NUM	EXP DT	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FORM	DOSE FREQ
127395212	12739521	1	SS	CONCERTA	METHYLPHENIDATE HYDROCHLORIDE	1	Unknown					U	5IE322		0	54	MG	SUSTAINED RELEASE TABLETS
127395212	12739521	2	PS	CONCERTA	METHYLPHENIDATE HYDROCHLORIDE	1	Unknown					U	5IE322		21121	36	MG	SUSTAINED RELEASE TABLETS

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
127395212	12739521	1	Attention deficit/hyperactivity disorder
127395212	12739521	2	Attention deficit/hyperactivity disorder

Outcome of event

Event ID	CASEID	OUTC COD
127395212	12739521	OT

Reactions reported

Event ID	CASEID	PT
127395212	12739521	Drug ineffective
127395212	12739521	Social problem
127395212	12739521	Treatment noncompliance

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	DUR	DUR COD
127395212	12739521	1	2013		0
127395212	12739521	2	201606		0