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
126015681 12601568 1 I 20160321 0 20160727 20160727 DIR 28.00 YR M N 140.00000 LBS 20160726 N 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
126015681 12601568 1 PS FINASTERIDE. FINASTERIDE 1 Oral N D 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126015681 12601568 1 Alopecia

Outcome of event

Event ID CASEID OUTC COD
126015681 12601568 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126015681 12601568 Appetite disorder
126015681 12601568 Asthenia
126015681 12601568 Balanoposthitis
126015681 12601568 Dry skin
126015681 12601568 Erectile dysfunction
126015681 12601568 Exercise tolerance decreased
126015681 12601568 Impaired healing
126015681 12601568 Insomnia
126015681 12601568 Libido decreased
126015681 12601568 Middle insomnia
126015681 12601568 Muscular weakness
126015681 12601568 Palpitations
126015681 12601568 Pollakiuria
126015681 12601568 Sleep disorder
126015681 12601568 Stress
126015681 12601568 Thirst decreased

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
126015681 12601568 1 20160110 20160111 0