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
127728091 12772809 1 I 201512 20160914 20160922 20160922 EXP PHHY2016FR128107 SANDOZ 82.69 YR M Y 0.00000 20160922 OT FR FR

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
127728091 12772809 1 SS TAREG VALSARTAN 1 Oral 160 MG, QD Y 0 160 MG QD
127728091 12772809 2 PS BISOPROLOL FUMARATE. BISOPROLOL FUMARATE 1 Oral 1.25 MG, QD Y U 75643 1.25 MG QD
127728091 12772809 3 SS ZOPICLONE ZOPICLONE 1 Oral 15 MG, QD Y U 0 15 MG TABLET QD
127728091 12772809 4 SS LASILIX FUROSEMIDE 1 Oral 20 MG, QD Y U 0 20 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127728091 12772809 1 Cardiac failure
127728091 12772809 2 Cardiac failure
127728091 12772809 3 Insomnia
127728091 12772809 4 Cardiac failure

Outcome of event

Event ID CASEID OUTC COD
127728091 12772809 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127728091 12772809 Diarrhoea
127728091 12772809 Renal failure

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
127728091 12772809 1 2013 20160826 0
127728091 12772809 2 201512 20160326 0
127728091 12772809 3 20160826 0
127728091 12772809 4 201512 20160826 0