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
127538811 12753881 1 I 20160823 20160916 20160916 EXP US-ROCHE-1829208 ROCHE 56.00 YR M Y 77.00000 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
127538811 12753881 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) COURSE 1 125085 1892 MG
127538811 12753881 2 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) COURSE 2 125085 866 MG
127538811 12753881 3 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) COURSE 1 0 100 MG
127538811 12753881 4 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) COURSE 2 0 100 MG
127538811 12753881 5 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) COURSE 3 0 100 MG
127538811 12753881 6 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) COURSE 4 0 75 MG
127538811 12753881 7 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) COURSE 5 0 75 MG
127538811 12753881 8 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) COURSE 6 0 100 MG
127538811 12753881 9 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) COURSE 7 0 100 MG
127538811 12753881 10 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) COURSE 8 0 100 MG
127538811 12753881 11 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) COURSE 9 0 100 MG
127538811 12753881 12 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) COURSE 10, LAST TREATMENT DATE: 26/OCT/2010 0 100 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127538811 12753881 1 Carcinoid tumour
127538811 12753881 3 Carcinoid tumour

Outcome of event

Event ID CASEID OUTC COD
127538811 12753881 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127538811 12753881 Hyperglycaemia
127538811 12753881 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
127538811 12753881 1 20100112 0
127538811 12753881 2 20100209 0
127538811 12753881 3 20100112 0
127538811 12753881 4 20100209 0
127538811 12753881 5 20100316 0
127538811 12753881 6 20100413 0
127538811 12753881 7 20100518 0
127538811 12753881 8 20100615 0
127538811 12753881 9 20100713 0
127538811 12753881 10 20100810 0
127538811 12753881 11 20100907 0
127538811 12753881 12 20101005 0