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
93544742 9354474 2 F 2012 20130625 20130618 20130630 EXP FR-TEVA-413066ISR TEVA 0.00 M Y 0.00000 20130630 MD 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
93544742 9354474 1 PS FUROSEMIDE TEVA 40mg 1 ORAL 165 MILLIGRAM DAILY; 125MG IN THE MORNING AND 40MG AT NOON D Y176 18413 TABLET
93544742 9354474 2 SS FUROSEMIDE TEVA 40mg 1 ORAL 80 MILLIGRAM DAILY; D Y176 18413
93544742 9354474 3 C Sevikar 40/10 2 D 0
93544742 9354474 4 C Esidrex 1 D 0
93544742 9354474 5 C Zyloric 1 D 0
93544742 9354474 6 C DIFFU K 1 D 0
93544742 9354474 7 C Novonorm 1 D 0
93544742 9354474 8 C Previscan 1 D 0
93544742 9354474 9 C Fluoxetine 1 D 0
93544742 9354474 10 C LASILIX 500 2 .25 TABLET DAILY; D 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
93544742 9354474 1 Cardiac disorder

Outcome of event

Event ID CASEID OUTC COD
93544742 9354474 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
93544742 9354474 Polyuria
93544742 9354474 Somnolence
93544742 9354474 Weight increased

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
93544742 9354474 1 20130609 0
93544742 9354474 2 20130609 0