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
126227911	12622791	1	I	2009	20150825	20160804	20160804	EXP		US-JNJFOC-20150821850	JANSSEN		0.00		A	F	Y	77.11000	KG	20160804		CN	US	US

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
126227911	12622791	1	SS	LEVAQUIN	LEVOFLOXACIN	1	Unknown				U	U			0	750	MG	UNSPECIFIED
126227911	12622791	2	PS	LEVAQUIN	LEVOFLOXACIN	1	Unknown				U	U			20634	750	MG	UNSPECIFIED

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
126227911	12622791	1	Sinusitis
126227911	12622791	2	Ear infection

Outcome of event

Event ID	CASEID	OUTC COD
126227911	12622791	DS
126227911	12622791	OT

Reactions reported

Event ID	CASEID	PT
126227911	12622791	Anxiety disorder
126227911	12622791	Depression
126227911	12622791	Insomnia
126227911	12622791	Neuropathy peripheral
126227911	12622791	Pain
126227911	12622791	Synovial cyst
126227911	12622791	Tendonitis
126227911	12622791	Tenosynovitis stenosans

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
126227911	12622791	1	20090208	20090218	0
126227911	12622791	2	20090208	20090218	0