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
126471151 12647115 1 I 20160731 0 20160811 20160811 DIR 72.00 YR F N 196.00000 LBS 20160809 N PH US

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
126471151 12647115 1 PS AUGMENTIN AMOXICILLINCLAVULANATE POTASSIUM 1 Oral D D 0 1 DF BID
126471151 12647115 2 SS ZOSYN PIPERACILLIN SODIUMTAZOBACTAM SODIUM 1 Intravenous (not otherwise specified) D D 0 50 ML Q8H

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126471151 12647115 1 Urinary tract infection
126471151 12647115 2 Sepsis
126471151 12647115 2 Urinary tract infection

Outcome of event

Event ID CASEID OUTC COD
126471151 12647115 OT
126471151 12647115 RI

Reactions reported

Event ID CASEID DRUG REC ACT PT
126471151 12647115 Acute hepatic failure

Reporting Sources (this data is often not reported and may therefore be missing here)

Event ID CASEID RPSR COD
126471151 12647115 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126471151 12647115 1 20160718 20160729 0
126471151 12647115 2 20160729 20160731 0