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
122377226	12237722	6	F	20150807	20160801	20160405	20160812	EXP		US-009507513-1604USA001867	MERCK		60.00	YR		F	Y	0.00000		20160812		OT	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
122377226	12237722	1	PS	PRIMAXIN IV	CILASTATIN SODIUMIMIPENEM	1		500 MG, 6-HOURLY AT DAY 4			Y	Y			50587	500	MG	INJECTION	Q6H
122377226	12237722	2	SS	PRIMAXIN IV	CILASTATIN SODIUMIMIPENEM	1		UNK			Y	Y			50587			INJECTION

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
122377226	12237722	1	Pneumonia escherichia

Outcome of event

Event ID	CASEID	OUTC COD
122377226	12237722	OT
122377226	12237722	LT

Reactions reported

Event ID	CASEID	DRUG REC ACT	PT
122377226	12237722		Acute respiratory distress syndrome
122377226	12237722	Eosinophilic pneumonia acute	Eosinophilic pneumonia acute
122377226	12237722		Respiratory failure

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
122377226	12237722	1	20150806	201508	0
122377226	12237722	2	20150827		0