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
127094591	12709459	1	I	20160828	20160828	20160902	20160902	EXP		CN-ROCHE-1821878	ROCHE		14.00	MON		M	Y	9.20000	KG	20160902		MD	CN	CN

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
127094591	12709459	1	PS	ROCEPHIN	CEFTRIAXONE SODIUM	1	Intravenous drip	1G/50ML			Y		UNKNOWN		63239	.6	G
127094591	12709459	2	C	MUCOSOLVAN	AMBROXOL HYDROCHLORIDE	1	Intravenous drip								0	10	MG

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
127094591	12709459	1	Pneumonia
127094591	12709459	2	Pneumonia

Outcome of event

Event ID	CASEID	OUTC COD
127094591	12709459	LT

Reactions reported

Event ID	CASEID	PT
127094591	12709459	Blood pressure increased
127094591	12709459	Cyanosis
127094591	12709459	Erythema
127094591	12709459	Pallor
127094591	12709459	Rales
127094591	12709459	Tachycardia

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
127094591	12709459	1	20160828	20160828	0
127094591	12709459	2	20160828		0