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
126262891	12626289	1	I	2012	20160728	20160805	20160805	EXP		US-AMGEN-USASP2016099148	AMGEN		34.00	YR	A	M	Y	0.00000		20160805		MD	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
126262891	12626289	1	PS	NEULASTA	PEGFILGRASTIM	1	Unknown	UNK							125031			SOLUTION FOR INJECTION

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
126262891	12626289	1	Product used for unknown indication

Outcome of event

Reactions reported

Event ID	CASEID	PT
126262891	12626289	Asthenia
126262891	12626289	Blood glucose decreased
126262891	12626289	Death
126262891	12626289	Dehydration
126262891	12626289	Metastases to liver
126262891	12626289	Pain
126262891	12626289	Seizure
126262891	12626289	Sickle cell anaemia with crisis

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
126262891	12626289	1	20121123	20121123	0