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
91721755	9172175	5	F	2004	20160711	20130319	20160714	PER		US-009507513-1303USA007566	MERCK		0.00			M	Y	122.45000	KG	20160714		CN	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
91721755	9172175	1	PS	PROPECIA	FINASTERIDE	1	Oral	1 MG, UNKNOWN			U				20788	1	MG	FILM-COATED TABLET

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
91721755	9172175	1	Androgenetic alopecia

Outcome of event

no results found

no results found

Reactions reported

Event ID	CASEID	PT
91721755	9172175	Back pain
91721755	9172175	Cognitive disorder
91721755	9172175	Dysuria
91721755	9172175	Erectile dysfunction
91721755	9172175	Genital hypoaesthesia
91721755	9172175	Haemorrhoids
91721755	9172175	Hand fracture
91721755	9172175	Hypogonadism male
91721755	9172175	Libido decreased
91721755	9172175	Lipids increased
91721755	9172175	Lung disorder
91721755	9172175	Orgasmic sensation decreased
91721755	9172175	Prostatitis
91721755	9172175	Sexual dysfunction

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
91721755	9172175	1	20030131	20101119	0