The Safety Rates Drug Report

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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
110260634 11026063 4 F 1998 20160802 20150414 20160808 EXP US-009507513-1504USA010771 MERCK 0.00 M Y 0.00000 20160808 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
110260634 11026063 1 PS PROPECIA FINASTERIDE 1 Oral 1 MG, QD 20788 1 MG FILM-COATED TABLET QD
110260634 11026063 2 SS PROPECIA FINASTERIDE 1 Oral 1 MG, UNK 20788 1 MG FILM-COATED TABLET
110260634 11026063 3 C LIPITOR ATORVASTATIN CALCIUM 1 Unknown UNK U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
110260634 11026063 1 Alopecia
110260634 11026063 3 Blood cholesterol increased

Outcome of event

Event ID CASEID OUTC COD
110260634 11026063 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
110260634 11026063 Anxiety
110260634 11026063 Brain injury
110260634 11026063 Depression
110260634 11026063 Ejaculation disorder
110260634 11026063 Endocrine disorder
110260634 11026063 Erectile dysfunction
110260634 11026063 Lactose intolerance
110260634 11026063 Loss of libido
110260634 11026063 Painful ejaculation
110260634 11026063 Penile size reduced
110260634 11026063 Sexual dysfunction
110260634 11026063 Soft tissue injury
110260634 11026063 Testicular atrophy

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
110260634 11026063 1 1998 200502 0
110260634 11026063 2 2006 0
110260634 11026063 3 1995 2001 0