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
124254322	12425432	2	F	20160308	20160705	20160601	20160707	EXP		JP-PFIZER INC-2016282188	PFIZER		78.00	YR		M	Y	47.50000	KG	20160707		MD	JP	JP

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	DOSE VBM	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FORM	DOSE FREQ
124254322	12425432	1	PS	RHEUMATREX	METHOTREXATE SODIUM	1	Oral	6 MG, WEEKLY	11719	6	MG	CAPSULE	/wk
124254322	12425432	2	SS	RHEUMATREX	METHOTREXATE SODIUM	1	Oral	8 MG, WEEKLY	11719	8	MG	CAPSULE	/wk
124254322	12425432	3	SS	RHEUMATREX	METHOTREXATE SODIUM	1	Oral	10 MG, WEEKLY	11719	10	MG	CAPSULE	/wk

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
124254322	12425432	1	Rheumatoid arthritis

Outcome of event

Reactions reported

Event ID	CASEID	PT
124254322	12425432	Arthralgia
124254322	12425432	Cardiac failure
124254322	12425432	Headache
124254322	12425432	Interstitial lung disease
124254322	12425432	Pyrexia

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
124254322	12425432	1	20141015	20141111
124254322	12425432	2	20141112	20150325
124254322	12425432	3	20150326	20160308