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
125730041 12573004 1 I 20160628 20160706 20160720 20160720 EXP GB-AUROBINDO-AUR-APL-2016-08940 AUROBINDO 69.00 YR M Y 70.00000 KG 20160720 MD GB GB

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
125730041 12573004 1 PS RAMIPRIL. RAMIPRIL 1 Unknown U U 91604
125730041 12573004 2 C FINASTERIDE. FINASTERIDE 1 Unknown 1 DF, ONCE A DAY 165.957993 DF U 0 1 DF QD
125730041 12573004 3 C SOLIFENACIN SOLIFENACIN 1 Unknown 1 DF, ONCE A DAY 165.957993 DF U 0 1 DF QD
125730041 12573004 4 C TAMSULOSIN HYDROCHLORIDE. TAMSULOSIN HYDROCHLORIDE 1 165.957993 DF U 0 1 DF QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125730041 12573004 1 Product used for unknown indication
125730041 12573004 2 Product used for unknown indication
125730041 12573004 3 Product used for unknown indication
125730041 12573004 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125730041 12573004 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125730041 12573004 Abdominal pain
125730041 12573004 Balance disorder
125730041 12573004 Chest pain
125730041 12573004 Confusional state
125730041 12573004 Muscle spasms
125730041 12573004 Myalgia

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
125730041 12573004 1 20160114 0
125730041 12573004 2 20160114 0
125730041 12573004 3 20160114 0
125730041 12573004 4 20160114 0