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
110447015 11044701 5 F 2003 20160708 20150417 20160712 EXP US-009507513-0907USA02883 MERCK 0.00 M Y 59.41000 KG 20160712 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
110447015 11044701 1 PS PROPECIA FINASTERIDE 1 Oral 1 MG, QD U 20788 1 MG FILM-COATED TABLET QD
110447015 11044701 2 SS FINASTERIDE. FINASTERIDE 1 Oral 1 MG, QD U 20788 1 MG FILM-COATED TABLET QD
110447015 11044701 3 SS FINASTERIDE. FINASTERIDE 1 Oral UNK U 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
110447015 11044701 1 Androgenetic alopecia
110447015 11044701 2 Androgenetic alopecia
110447015 11044701 3 Androgenetic alopecia

Outcome of event

Event ID CASEID OUTC COD
110447015 11044701 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
110447015 11044701 Alopecia
110447015 11044701 Anxiety
110447015 11044701 Brain injury
110447015 11044701 Depression
110447015 11044701 Drug ineffective
110447015 11044701 Endocrine disorder
110447015 11044701 Erectile dysfunction
110447015 11044701 Heart rate increased
110447015 11044701 Hormone level abnormal
110447015 11044701 Loss of libido
110447015 11044701 Painful ejaculation
110447015 11044701 Penis injury
110447015 11044701 Self esteem decreased
110447015 11044701 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
110447015 11044701 1 2001 201211 0
110447015 11044701 2 20031007 20090715 0
110447015 11044701 3 20130222 201311 0