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
127406931 12740693 1 I 20160823 20160914 20160914 EXP US-ROCHE-1828658 ROCHE 67.00 YR M Y 61.80000 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
127406931 12740693 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) COURSE 1 U 125085 1350 MG SOLUTION FOR INFUSION
127406931 12740693 2 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) COURSE 2 U 125085 1360 MG SOLUTION FOR INFUSION
127406931 12740693 3 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) COURSE 3 U 125085 1360 MG SOLUTION FOR INFUSION
127406931 12740693 4 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) COURSE 4 U 125085 1260 MG SOLUTION FOR INFUSION
127406931 12740693 5 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) COURSE 5 U 125085 1240 MG SOLUTION FOR INFUSION
127406931 12740693 6 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) COURSE 6 U 125085 1270 MG SOLUTION FOR INFUSION
127406931 12740693 7 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) COURSE 7 U 125085 1250 MG SOLUTION FOR INFUSION
127406931 12740693 8 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) COURSE 8 U 125085 1250 MG SOLUTION FOR INFUSION
127406931 12740693 9 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) COURSE 9 U 125085 1240 MG SOLUTION FOR INFUSION
127406931 12740693 10 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) COURSE 1 U 0 100 MG
127406931 12740693 11 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) COURSE 2 U 0 100 MG
127406931 12740693 12 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) COURSE 3 U 0 100 MG
127406931 12740693 13 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) COURSE 4 U 0 80 MG
127406931 12740693 14 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) COURSE 5 U 0 80 MG
127406931 12740693 15 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) COURSE 6 U 0 80 MG
127406931 12740693 16 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) COURSE 7 U 0 70 MG
127406931 12740693 17 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) COURSE 8 U 0 80 MG
127406931 12740693 18 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) COURSE 9 U 0 80 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127406931 12740693 1 Carcinoid tumour
127406931 12740693 10 Carcinoid tumour

Outcome of event

Event ID CASEID OUTC COD
127406931 12740693 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127406931 12740693 Blood bilirubin increased

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
127406931 12740693 1 20100118 0
127406931 12740693 2 20100215 0
127406931 12740693 3 20100315 0
127406931 12740693 4 20100412 0
127406931 12740693 5 20100510 0
127406931 12740693 6 20100607 0
127406931 12740693 7 20100706 0
127406931 12740693 8 20100803 0
127406931 12740693 9 20100831 0
127406931 12740693 10 20100118 0
127406931 12740693 11 20100215 0
127406931 12740693 12 20100315 0
127406931 12740693 13 20100412 0
127406931 12740693 14 20100510 0
127406931 12740693 15 20100607 0
127406931 12740693 16 20100706 0
127406931 12740693 17 20100803 0
127406931 12740693 18 20100831 0