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
126737331 12673733 1 I 20160630 20160811 20160822 20160822 EXP FR-SA-2016SA149380 AVENTIS 72.00 YR E F Y 0.00000 20160822 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
126737331 12673733 1 PS LOVENOX ENOXAPARIN SODIUM 1 Subcutaneous U UNKNOWN 20164
126737331 12673733 2 SS CIPROFLOXACIN HYDROCHLORIDE. CIPROFLOXACIN HYDROCHLORIDE 1 Intravenous (not otherwise specified) N UNKNOWN 0
126737331 12673733 3 SS PIPERACILLIN PIPERACILLIN 1 Intravenous (not otherwise specified) N UNKNOWN 0 4 G TID
126737331 12673733 4 SS PIPERACILLIN PIPERACILLIN 1 Intravenous (not otherwise specified) N UNKNOWN 0
126737331 12673733 5 SS COLCHICINE. COLCHICINE 1 Oral U UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126737331 12673733 1 Circulating anticoagulant
126737331 12673733 2 Infection
126737331 12673733 3 Infection
126737331 12673733 4 Infection
126737331 12673733 5 Gout

Outcome of event

Event ID CASEID OUTC COD
126737331 12673733 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126737331 12673733 Rash maculo-papular

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
126737331 12673733 1 20160625 0
126737331 12673733 2 20160617 20160630 0
126737331 12673733 3 20160606 0
126737331 12673733 4 20160628 20160630 0
126737331 12673733 5 20160624 0