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
80082862 8008286 2 F 20110426 20160823 20110624 20160930 EXP US-ROCHE-782838 ROCHE 59.00 YR F Y 102.00000 KG 20160930 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
80082862 8008286 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) LAST ADMINISTERED DATE:12/APR/2011,TOTAL DOSE THIS COURSE:1020 MG, OVER 30-90MIN ON DAY 1 AND 15. 125085 10 MG/KG SOLUTION FOR INFUSION
80082862 8008286 2 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) FREQUENCY: ON DAY 1,8,15 AND 22. LAST ADMINISTERED DATE: 19/APR/2011 0 25 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
80082862 8008286 1 Neoplasm malignant
80082862 8008286 2 Neoplasm malignant

Outcome of event

Event ID CASEID OUTC COD
80082862 8008286 OT
80082862 8008286 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
80082862 8008286 Acute kidney injury
80082862 8008286 Blood creatinine increased
80082862 8008286 Haematuria
80082862 8008286 Hypophosphataemia
80082862 8008286 Rectal haemorrhage

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found