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
92257313 9225731 3 F 2000 20160711 20130411 20160713 EXP US-009507513-1304USA002506 MERCK 0.00 M Y 0.00000 20160713 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
92257313 9225731 1 PS PROPECIA FINASTERIDE 1 Oral 1 MG QD 20788 1 MG FILM-COATED TABLET QD
92257313 9225731 2 SS PROPECIA FINASTERIDE 1 20788 FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
92257313 9225731 1 Androgenetic alopecia
92257313 9225731 2 Alopecia

Outcome of event

Event ID CASEID OUTC COD
92257313 9225731 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
92257313 9225731 Anxiety
92257313 9225731 Cognitive disorder
92257313 9225731 Erectile dysfunction
92257313 9225731 Hernia
92257313 9225731 Insomnia
92257313 9225731 Loss of libido
92257313 9225731 Oropharyngeal pain
92257313 9225731 Sexual dysfunction
92257313 9225731 Upper-airway cough syndrome

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
92257313 9225731 1 20000911 200911 0