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
127539711	12753971	1	I	2016	20160823	20160915	20160915	EXP		US-UCBSA-2016032914	UCB		60.45	YR		F	Y	0.00000		20160915		OT	US	US

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	DOSE VBM	DECHAL	RECHAL	LOT NUM	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FORM	DOSE FREQ
127539711	12753971	1	PS	CIMZIA	CERTOLIZUMAB PEGOL	1	Subcutaneous	200 MG, EV 2 WEEKS(QOW) (EXPIRY DATE: 30-NOV-2017 00:00)	U		902023, 902721	125160	200	MG	SOLUTION FOR INJECTION	QOW
127539711	12753971	2	C	Tamsulosin	TAMSULOSIN	1		UNK		U		0
127539711	12753971	3	C	LYRICA	PREGABALIN	1		UNK		U		0
127539711	12753971	4	C	CARISOPRODOL.	CARISOPRODOL	1				U		0
127539711	12753971	5	C	TRAMADOL.	TRAMADOL	1				U		0
127539711	12753971	6	C	OMEPRAZOLE.	OMEPRAZOLE	1				U		0
127539711	12753971	7	C	PREMARIN	ESTROGENS, CONJUGATED	1				U		0
127539711	12753971	8	C	Cyclobenzaprine	CYCLOBENZAPRINE	1				U		0
127539711	12753971	9	C	FLOMAX	TAMSULOSIN HYDROCHLORIDE	1		UNK		U		0
127539711	12753971	10	C	BACTRIM	SULFAMETHOXAZOLETRIMETHOPRIM	1		UNK		U		0

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
127539711	12753971	1	Product used for unknown indication
127539711	12753971	2	Product used for unknown indication
127539711	12753971	3	Product used for unknown indication
127539711	12753971	4	Product used for unknown indication
127539711	12753971	5	Product used for unknown indication
127539711	12753971	6	Product used for unknown indication
127539711	12753971	7	Product used for unknown indication
127539711	12753971	8	Product used for unknown indication
127539711	12753971	9	Nephrolithiasis
127539711	12753971	10	Nephrolithiasis

Outcome of event

Event ID	CASEID	OUTC COD
127539711	12753971	OT

Reactions reported

Event ID	CASEID	PT
127539711	12753971	Diarrhoea
127539711	12753971	Drug dose omission
127539711	12753971	Nephrolithiasis
127539711	12753971	Pain
127539711	12753971	Renal disorder

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
127539711	12753971	1	201604	2016
127539711	12753971	9	2016
127539711	12753971	10	2016