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
127408001 12740800 1 I 20100727 20110607 20160914 20160914 EXP US-ROCHE-783389 ROCHE 68.57 YR F Y 87.70000 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
127408001 12740800 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) OVER 30-90 MIN ON DAYS 1 AND 15, LAST ADMINISTRATION DATE OF IND: 08/JUL/2010 125085 1824 MG SOLUTION FOR INFUSION
127408001 12740800 2 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) ON DAYS 1,8, 15, 22, LAST ADMINISTRATION DATE OF IND: 08 APRIL 2010 0 50 MG
127408001 12740800 3 C ALLOPURINOL. ALLOPURINOL 1 Unknown 0
127408001 12740800 4 C K CITRATE 2 0
127408001 12740800 5 C ZOLOFT SERTRALINE HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127408001 12740800 1 Carcinoid tumour
127408001 12740800 2 Carcinoid tumour

Outcome of event

Event ID CASEID OUTC COD
127408001 12740800 HO
127408001 12740800 DE
127408001 12740800 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127408001 12740800 Fatigue
127408001 12740800 Large intestine perforation
127408001 12740800 Rash maculo-papular

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
127408001 12740800 1 20100401 0