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
127525761 12752576 1 I 20100908 20110607 20160916 20160916 EXP US-ROCHE-783504 ROCHE 80.00 YR F Y 0.00000 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
127525761 12752576 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) 10 MG/KG?OVER 30 TO 90 MIN ON DAYS 1 AND 15 (28 DAYS CYCLE)?LAST DOSE PRIOR TO SAE: 31 AUGUST 2010 U 125085 1400 MG SOLUTION FOR INFUSION
127525761 12752576 2 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) U 125085 610 MG
127525761 12752576 3 SS Bevacizumab BEVACIZUMAB 1 U 125085
127525761 12752576 4 SS Bevacizumab BEVACIZUMAB 1 U 125085
127525761 12752576 5 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) 25 MG?DAYS 1, 8, 15, 22 (28 DAY CYCLE)?LAST DOSE PRIOR TO SAE: 31 AUGUST 2010 U 0 100 MG
127525761 12752576 6 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) U 0 25 MG
127525761 12752576 7 SS TEMSIROLIMUS TEMSIROLIMUS 1 U 0
127525761 12752576 8 SS TEMSIROLIMUS TEMSIROLIMUS 1 U 0
127525761 12752576 9 SS PERCOCET ACETAMINOPHENOXYCODONE HYDROCHLORIDE 1 Unknown U 0
127525761 12752576 10 C COMPAZINE PROCHLORPERAZINE MALEATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127525761 12752576 1 Endometrial cancer
127525761 12752576 2 Ovarian cancer
127525761 12752576 3 Malignant neoplasm of islets of Langerhans
127525761 12752576 4 Hepatocellular carcinoma
127525761 12752576 5 Endometrial cancer
127525761 12752576 6 Hepatocellular carcinoma
127525761 12752576 7 Malignant neoplasm of islets of Langerhans
127525761 12752576 8 Ovarian cancer
127525761 12752576 9 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127525761 12752576 OT
127525761 12752576 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127525761 12752576 Anaemia
127525761 12752576 Ileus
127525761 12752576 Infection
127525761 12752576 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