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
124411593 12441159 3 F 20140704 20160708 20160607 20160711 EXP DE-ROCHE-1482337 ROCHE 50.00 YR F Y 83.70000 KG 20160711 MD DE DE

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
124411593 12441159 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) LAST DOSE PRIOR TOSAE: 04/JUL/2014 Y 125085 847 MG QOW
124411593 12441159 2 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) LAST DOSE PRIOR TO SAE: 15/AUG/2014 Y 125085 820 MG QOW
124411593 12441159 3 SS PACLITAXEL. PACLITAXEL 1 Intravenous (not otherwise specified) LAST DOSE PRIOR TO SAE: 04/JUL/2014 U 0 176 MG /wk
124411593 12441159 4 SS PACLITAXEL. PACLITAXEL 1 Intravenous (not otherwise specified) ALSO RECEIVED ON 22/AUG/2014 U 0 174 MG /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124411593 12441159 1 Breast cancer
124411593 12441159 3 Breast cancer

Outcome of event

Event ID CASEID OUTC COD
124411593 12441159 LT
124411593 12441159 HO
124411593 12441159 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124411593 12441159 Diverticulum intestinal
124411593 12441159 Hypertension
124411593 12441159 Intestinal perforation
124411593 12441159 Large intestinal stenosis

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
124411593 12441159 1 20140327 0
124411593 12441159 2 20140815 20140815 0
124411593 12441159 3 20140327 20140801 0
124411593 12441159 4 20140815 0