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
127413111 12741311 1 I 20101025 20110607 20160914 20160914 EXP US-ROCHE-782398 ROCHE 65.23 YR M Y 51.90000 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
127413111 12741311 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) ON DAY 1, AND 15 DATE OF LAST ADMINISTRATION WAS 19 OCTOBER 2010 U 125085 10 MG/KG SOLUTION FOR INFUSION
127413111 12741311 2 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) DAY 1, 8, 15 AND 22, LAST DOSE ADMINISTERED ON 19 OCTOBER 2010, CYCLE 28 U 0 25 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127413111 12741311 1 Carcinoid tumour
127413111 12741311 2 Carcinoid tumour

Outcome of event

Event ID CASEID OUTC COD
127413111 12741311 DE
127413111 12741311 HO
127413111 12741311 LT
127413111 12741311 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127413111 12741311 Abdominal pain
127413111 12741311 Anaemia
127413111 12741311 Disseminated intravascular coagulation
127413111 12741311 Gastrointestinal perforation
127413111 12741311 Haematoma
127413111 12741311 Haematuria
127413111 12741311 Hypokalaemia
127413111 12741311 Hypoxia
127413111 12741311 Lower gastrointestinal haemorrhage
127413111 12741311 Small intestinal obstruction

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found