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
126109521	12610952	1	I	201008	20160623	20160801	20160801	EXP		CA-BAYER-2016-124361	BAYER		60.00	YR	A	M	Y	90.72000	KG	20160801		CN	CA	CA

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
126109521	12610952	1	PS	AVELOX	MOXIFLOXACIN HYDROCHLORIDE	1	Oral	400 MG, QD					DIN 02242965		21085	400	MG	FILM-COATED TABLET	QD
126109521	12610952	2	C	PARIET	RABEPRAZOLE SODIUM	1		10 MG, UNK							0	10	MG

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
126109521	12610952	1	Chronic sinusitis
126109521	12610952	2	Gastrooesophageal reflux disease

Outcome of event

Event ID	CASEID	OUTC COD
126109521	12610952	OT
126109521	12610952	HO

Reactions reported

Event ID	CASEID	PT
126109521	12610952	Arthralgia
126109521	12610952	Arthritis
126109521	12610952	Formication
126109521	12610952	Muscle spasms
126109521	12610952	Neuropathy peripheral
126109521	12610952	Pain in extremity
126109521	12610952	Sensory loss
126109521	12610952	Stiff person syndrome
126109521	12610952	Tendon rupture
126109521	12610952	Tendonitis
126109521	12610952	Toxicity to various agents

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
126109521	12610952	1	20100815	20100820	0
126109521	12610952	2	200006		0