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
98045538 9804553 8 F 2009 20160728 20140108 20160805 EXP US-009507513-1109USA02522 MERCK 0.00 M Y 97.51000 KG 20160805 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
98045538 9804553 1 PS PROPECIA FINASTERIDE 1 Oral UNK UNK, UNKNOWN U 20788 FILM-COATED TABLET
98045538 9804553 2 SS PROPECIA FINASTERIDE 1 Oral UNK, UNKNOWN U 20788 1 MG FILM-COATED TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
98045538 9804553 1 Alopecia

Outcome of event

Event ID CASEID OUTC COD
98045538 9804553 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
98045538 9804553 Anxiety
98045538 9804553 Emotional distress
98045538 9804553 Erectile dysfunction
98045538 9804553 High risk sexual behaviour
98045538 9804553 Loss of libido
98045538 9804553 Nasal polyps
98045538 9804553 Orgasmic sensation decreased
98045538 9804553 Semen analysis abnormal
98045538 9804553 Sexual dysfunction
98045538 9804553 Testicular pain
98045538 9804553 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
98045538 9804553 1 2005 0
98045538 9804553 2 20050301 201005 0