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
125593671 12559367 1 I 20160628 20160706 20160715 20160715 EXP GB-MHRA-ADR 23542239 GB-ACCORD-042310 ACCORD 69.00 YR M Y 70.00000 KG 20160715 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
125593671 12559367 1 PS RAMIPRIL. RAMIPRIL 1 U 202392
125593671 12559367 2 C FINASTERIDE. FINASTERIDE 1 165.96 DF 0 1 DF QD
125593671 12559367 3 C SOLIFENACIN/SOLIFENACIN SUCCINATE 2 165.96 DF 0 1 DF QD
125593671 12559367 4 C TAMSULOSIN TAMSULOSIN 1 165.96 DF 0 1 DF QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125593671 12559367 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125593671 12559367 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125593671 12559367 Abdominal pain
125593671 12559367 Balance disorder
125593671 12559367 Chest pain
125593671 12559367 Confusional state
125593671 12559367 Muscle spasms
125593671 12559367 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
125593671 12559367 1 20160114 0
125593671 12559367 2 20160114 0
125593671 12559367 3 20160114 0
125593671 12559367 4 20160114 0