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
127907981 12790798 1 I 20160823 20160929 20160929 EXP US-ROCHE-1835398 ROCHE 64.00 YR F Y 48.00000 KG 20160929 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
127907981 12790798 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) OVER 30-90 MINUTES ON DAY1 AND DAY15 EVERY 28 DAYS U 125085 1080 MG
127907981 12790798 2 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) OVER 30-90 MINUTES ON DAY1, 8, 15 AND 22 EVERY 28 DAYS U 0 100 MG
127907981 12790798 3 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) OVER 30-90 MINUTES ON DAY1, 8, 15 AND 22 EVERY 28 DAYS U 0 75 MG
127907981 12790798 4 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) OVER 30-90 MINUTES ON DAY1, 8, 15 AND 22 EVERY 28 DAYS U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127907981 12790798 1 Carcinoid tumour
127907981 12790798 2 Carcinoid tumour

Outcome of event

Event ID CASEID OUTC COD
127907981 12790798 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127907981 12790798 Anal fistula
127907981 12790798 Blood bilirubin increased
127907981 12790798 Haemorrhoids

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
127907981 12790798 1 20101210 0
127907981 12790798 2 20101210 0
127907981 12790798 3 20110118 0
127907981 12790798 4 20110214 0