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
127453071 12745307 1 I 20091110 20110621 20160915 20160915 EXP US-ROCHE-785836 ROCHE 56.00 YR F Y 108.60000 KG 20160915 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
127453071 12745307 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) CYCLE-28 DAYS-GIVEN OVER 30-90 MIN ON DAYS 1 AND 15, TOTAL DOSE:1130 MG, LAST DOSE:05 JAN 2010 U 125085 10 MG/KG SOLUTION FOR INFUSION
127453071 12745307 2 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) CYCLE-28 DAYS-GIVEN ON DAYS 1, 8, 15, 22, TOTAL DOSE:40 MG, LAST DOSE:12 JAN 2010 U 0 25 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127453071 12745307 1 Ovarian neoplasm
127453071 12745307 2 Neoplasm malignant

Outcome of event

Event ID CASEID OUTC COD
127453071 12745307 OT
127453071 12745307 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127453071 12745307 Blood bilirubin increased
127453071 12745307 Chills
127453071 12745307 Hyponatraemia
127453071 12745307 Lymphocyte count decreased
127453071 12745307 Neutrophil count decreased
127453071 12745307 Platelet count decreased
127453071 12745307 Pyrexia
127453071 12745307 Skin infection
127453071 12745307 White blood cell count decreased

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

no results found

Therapies reported

no results found