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
127525201 12752520 1 I 20101106 20150710 20160916 20160916 EXP US-ROCHE-1670552 ROCHE 52.00 YR M Y 78.90000 KG 20160916 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
127525201 12752520 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) OVER 30-90 MIN ON DAYS 1 AND 15?28 DAYS CYCLE?DATE OF LAST DOSE PRIOR TO SAE: 29/OCT/2010 U 125085 10 MG/KG SOLUTION FOR INFUSION
127525201 12752520 2 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) ON DAYS 1, 8, 15, 22?28 DAYS CYCLE?DATE OF LAST DOSE PRIOR TO SAE: 05/NOV/2010 U 0 25 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127525201 12752520 1 Carcinoid tumour
127525201 12752520 2 Carcinoid tumour

Outcome of event

Event ID CASEID OUTC COD
127525201 12752520 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127525201 12752520 Diarrhoea
127525201 12752520 Epistaxis
127525201 12752520 Gout
127525201 12752520 Hypertension
127525201 12752520 Pulmonary haemorrhage
127525201 12752520 Sinus disorder

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
127525201 12752520 1 20100528 0
127525201 12752520 2 20100528 0