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
73762433 7376243 3 F 20100330 20160823 20100504 20160914 EXP US-ROCHE-700747 ROCHE 58.00 YR F Y 74.00000 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
73762433 7376243 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) LAST DOSE OF BEVACIZUMAB ON 16 MARCH 2010, OVER 30-90 MINUTES ON DAYS 1 AND 15?DATE OF LAST TREATMEN Y 125085 10 MG/KG SOLUTION FOR INFUSION
73762433 7376243 2 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) TEMSIROLIMUS 25 MG ON DAY 1,8,15 AND 22, LAST DOSE OF DRUG WAS ON 23 MARCH 2010 (CYCLE 4. DAY8).?DAT 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
73762433 7376243 1 Carcinoid tumour
73762433 7376243 2 Carcinoid tumour

Outcome of event

Event ID CASEID OUTC COD
73762433 7376243 OT
73762433 7376243 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
73762433 7376243 Blood bilirubin increased
73762433 7376243 Cardiac failure congestive
73762433 7376243 Hypertension
73762433 7376243 Hypoxia
73762433 7376243 Left ventricular dysfunction
73762433 7376243 Platelet count decreased
73762433 7376243 Pneumonitis
73762433 7376243 Wound dehiscence

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

no results found

Therapies reported

no results found