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
94107093 9410709 3 F 2000 20160823 20130719 20160826 EXP US-009507513-1307USA008321 MERCK 0.00 M Y 0.00000 20160826 MD 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
94107093 9410709 1 PS PROPECIA FINASTERIDE 1 Oral 1 MG, UNK 20788 1 MG FILM-COATED TABLET QD
94107093 9410709 2 SS FINASTERIDE. FINASTERIDE 1 Oral UNK, UNKNOWN U 0 FILM-COATED TABLET
94107093 9410709 3 SS FINASTERIDE. FINASTERIDE 1 Oral 5 MG, UNKNOWN U 0 5 MG TABLET
94107093 9410709 4 C AMLODIPINE AMLODIPINE BESYLATE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
94107093 9410709 1 Androgenetic alopecia
94107093 9410709 2 Product used for unknown indication
94107093 9410709 3 Product used for unknown indication
94107093 9410709 4 Hypertension

Outcome of event

Event ID CASEID OUTC COD
94107093 9410709 DS
94107093 9410709 OT
94107093 9410709 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
94107093 9410709 Anxiety
94107093 9410709 Cardiac disorder
94107093 9410709 Cardiac failure congestive
94107093 9410709 Cognitive disorder
94107093 9410709 Depression
94107093 9410709 Erectile dysfunction
94107093 9410709 Heart transplant
94107093 9410709 Libido decreased
94107093 9410709 Prostatomegaly
94107093 9410709 Rash
94107093 9410709 Renal transplant
94107093 9410709 Sexual dysfunction

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
94107093 9410709 1 1998 20130712 0
94107093 9410709 3 201506 201607 0