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
126101201 12610120 1 I 20160727 0 20160729 20160729 DIR 39.00 YR M N 140.00000 LBS 20160728 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
126101201 12610120 1 PS FINASTERIDE. FINASTERIDE 1 Oral N Y 20171001 0 QD
126101201 12610120 3 C KLONOPIN CLONAZEPAM 1 0
126101201 12610120 5 C PROZAC FLUOXETINE HYDROCHLORIDE 1 0
126101201 12610120 7 C RODHIOLA ROSEA 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126101201 12610120 1 Alopecia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126101201 12610120 Alopecia
126101201 12610120 Drug ineffective
126101201 12610120 Product substitution issue

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
126101201 12610120 1 20160701 20160727 0