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
124618333 12461833 3 F 2015 20160706 20160613 20160713 EXP US-SA-2016SA110553 AVENTIS 0.00 A F Y 0.00000 20160713 CN US 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
124618333 12461833 1 SS FLUOROURACIL. FLUOROURACIL 1 Unknown Y UNKNOWN 0
124618333 12461833 2 PS OXALIPLATIN. OXALIPLATIN 1 Unknown Y UNKNOWN 21759
124618333 12461833 3 SS CALCIUM FOLINATE LEUCOVORIN CALCIUM 1 Unknown Y UNKNOWN 0
124618333 12461833 4 C VALIUM DIAZEPAM 1 Oral 0 10 MG TABLET TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124618333 12461833 1 Hepatic cancer
124618333 12461833 2 Product used for unknown indication
124618333 12461833 3 Product used for unknown indication
124618333 12461833 4 Meniere's disease

Outcome of event

Event ID CASEID OUTC COD
124618333 12461833 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124618333 12461833 Alopecia
124618333 12461833 Memory impairment
124618333 12461833 Transient ischaemic attack

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
124618333 12461833 1 201505 0
124618333 12461833 2 201505 0
124618333 12461833 3 201505 0