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
127524131 12752413 1 I 20100412 20110721 20160915 20160915 EXP US-ROCHE-792283 ROCHE 54.00 YR F Y 43.00000 KG 20160916 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
127524131 12752413 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) 10 MG/KG IV OVER 30-90 MIN ON DAY 1 AND 15, LAST DOSE ADMINISTERED: 12 APRIL 2010, TOTAL DOSE:549 MG 125085 10 MG/KG SOLUTION FOR INFUSION
127524131 12752413 2 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) 25 MG IV ON DAYS 1,8, 15, 22, LAST DOSE ADMINISTERED:12 APRIL 2010, TOTAL DOSE: 20 MG?DATE OF LAST T 0 25 MG
127524131 12752413 3 C Granisetron GRANISETRON 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127524131 12752413 1 Malignant neoplasm of islets of Langerhans
127524131 12752413 2 Malignant neoplasm of islets of Langerhans

Outcome of event

Event ID CASEID OUTC COD
127524131 12752413 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127524131 12752413 Abdominal pain
127524131 12752413 Acute kidney injury
127524131 12752413 Anaemia
127524131 12752413 Asthenia
127524131 12752413 Fatigue
127524131 12752413 Hyperkalaemia
127524131 12752413 Pain

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

no results found

Therapies reported

no results found