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
125615641 12561564 1 I 20160628 20160706 20160715 20160715 EXP GB-MHRA-TPP1504729C198044YC1467096108513 PHHY2016GB093358 SANDOZ 69.00 YR M Y 70.00000 KG 20160715 OT 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
125615641 12561564 1 PS RAMIPRIL. RAMIPRIL 1 Unknown U 77514
125615641 12561564 2 C FINASTERIDE. FINASTERIDE 1 Unknown 1 DF, QD 165.957993 DF U 0 1 DF QD
125615641 12561564 3 C SOLIFENACIN SOLIFENACIN 1 Unknown 1 DF, QD 165.957993 DF U 0 1 DF QD
125615641 12561564 4 C TAMSULOSIN HYDROCHLORIDE. TAMSULOSIN HYDROCHLORIDE 1 Unknown 1 DF, QD 165.957993 DF U 0 1 DF QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125615641 12561564 1 Product used for unknown indication
125615641 12561564 2 Product used for unknown indication
125615641 12561564 3 Product used for unknown indication
125615641 12561564 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125615641 12561564 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125615641 12561564 Abdominal pain
125615641 12561564 Balance disorder
125615641 12561564 Chest pain
125615641 12561564 Confusional state
125615641 12561564 Muscle spasms
125615641 12561564 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
125615641 12561564 1 20160114 0
125615641 12561564 2 20160114 0
125615641 12561564 3 20160114 0
125615641 12561564 4 20160114 0