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
127964361 12796436 1 I 20150309 20160921 20160929 20160929 EXP IT-SA-2016SA176983 AVENTIS 0.00 A F Y 0.00000 20160929 PH IT IT

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
127964361 12796436 1 PS CLEXANE ENOXAPARIN SODIUM 1 Subcutaneous Y UNKNOWN 20164 SOLUTION FOR INJECTION QD
127964361 12796436 2 SS TAZOCIN PIPERACILLIN SODIUMTAZOBACTAM SODIUM 1 Intravenous (not otherwise specified) Y UNKNOWN 0 4.5 G SOLUTION FOR INJECTION QD
127964361 12796436 3 SS VANCOMYCIN VANCOMYCIN 1 Intravenous (not otherwise specified) Y UNKNOWN 0 2 G POWDER FOR SOLUTION FOR INJECTION QD
127964361 12796436 4 C PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Oral 0 200 MG FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127964361 12796436 1 Thrombosis prophylaxis
127964361 12796436 2 Enterococcal sepsis
127964361 12796436 3 Enterococcal sepsis
127964361 12796436 4 Systemic lupus erythematosus

Outcome of event

Event ID CASEID OUTC COD
127964361 12796436 OT
127964361 12796436 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127964361 12796436 Diarrhoea
127964361 12796436 Platelet count decreased
127964361 12796436 Rash 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
127964361 12796436 1 20150109 20150113 0
127964361 12796436 2 20150308 20150313 0
127964361 12796436 3 20150307 20150310 0