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
124859212	12485921	2	F	20160617	20160805	20160621	20160810	EXP		PHJP2016JP017156	NOVARTIS		57.00	YR		F	Y	0.00000		20160810		MD	JP	JP

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	DOSE VBM	DECHAL	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FORM
124859212	12485921	1	PS	TEGRETOL	CARBAMAZEPINE	1	Oral	400 MG, UNK	Y	16608	400	MG	TABLET
124859212	12485921	2	C	DEPAS	ETIZOLAM	1	Oral	1.5 MG, UNK	Y	0	1.5	MG	TABLET
124859212	12485921	3	C	TELMISARTAN.	TELMISARTAN	1	Oral	80 MG, UNK	Y	0	80	MG	TABLET

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
124859212	12485921	1	Epilepsy
124859212	12485921	2	Product used for unknown indication
124859212	12485921	3	Product used for unknown indication

Outcome of event

Event ID	CASEID	OUTC COD
124859212	12485921	HO

Reactions reported

Event ID	CASEID	PT
124859212	12485921	Dizziness
124859212	12485921	Hyponatraemia
124859212	12485921	Inappropriate antidiuretic hormone secretion

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
124859212	12485921	1	20110317	20160614
124859212	12485921	2	20111026	20160614
124859212	12485921	3	20110831	20160614