The Safety Rates Drug Report

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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
127972741 12797274 1 I 20160823 20160930 20160930 EXP CA-ROCHE-1833049 ROCHE 73.00 YR M Y 64.40000 KG 20160930 MD CA CA

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
127972741 12797274 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) OVER 30-90 MINUTES ON DAY 1 AND DAY 15 IN 28 DAYS CYCLE?ALSO RECEIVED ON 24/AUG/2010, 21/SEP/2010, 1 U 125085 1476 MG
127972741 12797274 2 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) OVER 30-90 MINUTES ON DAY 1 AND DAY 15 IN 28 DAYS CYCLE?ALSO RECIEVED ON 08/FEB/2011 U 125085 644 MG
127972741 12797274 3 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) OVER 30-90 MINUTES ON DAY 1 AND DAY 15 IN 28 DAYS CYCLE?ALSO RECEIVED ON 11/JAN/2011 U 125085 1288 MG
127972741 12797274 4 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) ON DAYS 1, 8, 15 AND 22 EVERY 28 DAYS?ALSO RECEIVED ON 24/AUG/2010, 21/SEP/2010 U 0 100 MG
127972741 12797274 5 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) ON DAYS 1, 8, 15 AND 22 EVERY 28 DAYS U 0 80 MG
127972741 12797274 6 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) ON DAYS 1, 8, 15 AND 22 EVERY 28 DAYS U 0 35 MG
127972741 12797274 7 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) ON DAYS 1, 8, 15 AND 22 EVERY 28 DAYS U 0 45 MG
127972741 12797274 8 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) ON DAYS 1, 8, 15 AND 22 EVERY 28 DAYS U 0 40 MG
127972741 12797274 9 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) ON DAYS 1, 8, 15 AND 22 EVERY 28 DAYS U 0 20 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127972741 12797274 1 Hepatocellular carcinoma
127972741 12797274 4 Hepatocellular carcinoma

Outcome of event

Event ID CASEID OUTC COD
127972741 12797274 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127972741 12797274 Anaemia

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
127972741 12797274 1 20100727 0
127972741 12797274 2 20101116 0
127972741 12797274 3 20101214 0
127972741 12797274 4 20100727 0
127972741 12797274 5 20101019 0
127972741 12797274 6 20101116 0
127972741 12797274 7 20101214 0
127972741 12797274 8 20110111 0
127972741 12797274 9 20110208 0