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
127163171 12716317 1 I 20160823 20160906 20160906 EXP US-ROCHE-1825832 ROCHE 75.00 YR M Y 64.10000 KG 20160906 MD 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
127163171 12716317 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) DATE OF MOST RECENT DOSE: 20/APR/2013 U 125085 15 MG/KG SOLUTION FOR INFUSION Q3W
127163171 12716317 2 SS IXABEPILONE IXABEPILONE 1 Intravenous (not otherwise specified) DATE OF MOST RECENT DOSE: 20/APR/2013 U 0 6 MG/M**2 INFUSION QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127163171 12716317 1 Clear cell renal cell carcinoma
127163171 12716317 2 Clear cell renal cell carcinoma

Outcome of event

Event ID CASEID OUTC COD
127163171 12716317 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127163171 12716317 Anaemia
127163171 12716317 Dyspnoea
127163171 12716317 Fatigue
127163171 12716317 Hypoalbuminaemia
127163171 12716317 Hypophosphataemia
127163171 12716317 Oesophageal haemorrhage

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
127163171 12716317 1 20130305 0