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
127555931 12755593 1 I 20110711 20110809 20160916 20160916 EXP US-ROCHE-796198 ROCHE 61.00 YR F Y 61.00000 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
127555931 12755593 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) D 125085 1273 MG
127555931 12755593 2 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) 0 85 MG
127555931 12755593 3 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) REDUCED DOSE 0 15 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127555931 12755593 1 Carcinoid tumour
127555931 12755593 2 Carcinoid tumour

Outcome of event

Event ID CASEID OUTC COD
127555931 12755593 OT
127555931 12755593 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127555931 12755593 Acute kidney injury
127555931 12755593 Anaemia
127555931 12755593 Clostridium difficile infection
127555931 12755593 Dehydration
127555931 12755593 Haematochezia
127555931 12755593 Haematuria
127555931 12755593 Hypertension
127555931 12755593 Hypophosphataemia
127555931 12755593 Small intestinal obstruction
127555931 12755593 Stoma site ulcer
127555931 12755593 Wound dehiscence

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
127555931 12755593 1 20100430 20121109 0
127555931 12755593 3 20100618 20121109 0