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
125866101	12586610	1	I	20160624	0	20160722	20160722	DIR					74.00	YR		F	N	140.00000	LBS	20160718	Y		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
125866101	12586610	1	PS	PREMPRO	ESTROGENS, CONJUGATEDMEDROXYPROGESTERONE ACETATE	1	Oral				Y	Y	N34134,M26181	201709,2	0	1	DF	COATED TABLET	QD

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
125866101	12586610	1	Menopausal symptoms

Outcome of event

Event ID	CASEID	OUTC COD
125866101	12586610	OT

Reactions reported

Event ID	CASEID	PT
125866101	12586610	Asthenia
125866101	12586610	Haemoptysis
125866101	12586610	Headache
125866101	12586610	Influenza like illness
125866101	12586610	Lower respiratory tract infection
125866101	12586610	Oropharyngeal pain
125866101	12586610	Productive cough
125866101	12586610	Pyrexia
125866101	12586610	Sinusitis

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
125866101	12586610	1	20160624	201607	0