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
127413191 12741319 1 I 20100202 20150710 20160914 20160914 EXP US-ROCHE-1665949 ROCHE 72.00 YR M Y 65.10000 KG 20160914 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
127413191 12741319 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) OVER 30-90 MINUTES ON DAY 1. U 125085 15 MG/KG
127413191 12741319 2 SS LENALIDOMIDE LENALIDOMIDE 1 Oral U 0 QD
127413191 12741319 3 SS DOCETAXEL. DOCETAXEL 1 Intravenous (not otherwise specified) OVER 60 MINUTES ON DAY 1 U 0 75 MG/M**2
127413191 12741319 4 SS PREDNISONE. PREDNISONE 1 Oral U 0 5 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127413191 12741319 1 Prostate cancer
127413191 12741319 2 Prostate cancer
127413191 12741319 3 Prostate cancer
127413191 12741319 4 Prostate cancer

Outcome of event

Event ID CASEID OUTC COD
127413191 12741319 HO
127413191 12741319 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127413191 12741319 Anaemia
127413191 12741319 Dehydration
127413191 12741319 Febrile neutropenia
127413191 12741319 Neutrophil count decreased

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
127413191 12741319 1 20100125 0
127413191 12741319 2 20100125 0
127413191 12741319 3 20100125 0
127413191 12741319 4 20100125 0