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
127323741	12732374	1	I	20160620	20160906	20160912	20160912	EXP		PHHO2016FR013123	NOVARTIS		64.47	YR		M	Y	0.00000		20160912		MD	FR	FR

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	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FREQ
127323741	12732374	1	PS	CERTICAN	EVEROLIMUS	1	Oral	9.5 MG, BID	209	MG	N	21560	9.5	MG	BID
127323741	12732374	2	SS	SOLU-MEDROL	METHYLPREDNISOLONE SODIUM SUCCINATE	1	Unknown	250 MG, QD				0	250	MG	QD
127323741	12732374	3	C	TACROLIMUS.	TACROLIMUS	1	Unknown	9 MG, QD				0	9	MG	QD

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
127323741	12732374	1	Renal transplant
127323741	12732374	2	Renal transplant
127323741	12732374	3	Renal transplant

Outcome of event

Event ID	CASEID	OUTC COD
127323741	12732374	LT
127323741	12732374	HO

Reactions reported

Event ID	CASEID	PT
127323741	12732374	Acute kidney injury
127323741	12732374	Acute pulmonary oedema
127323741	12732374	Kidney transplant rejection
127323741	12732374	Septic shock

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
127323741	12732374	1	20160614	20160624
127323741	12732374	2	20160614
127323741	12732374	3	20160614