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
127905511 12790551 1 I 20160823 20160929 20160929 EXP US-ROCHE-1834233 ROCHE 74.00 YR F Y 78.60000 KG 20160929 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
127905511 12790551 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) LAST TREATMENT RECIEVED ON 31/AUG/2011 U 125085 SOLUTION FOR INFUSION
127905511 12790551 2 SS PACLITAXEL. PACLITAXEL 1 Intravenous (not otherwise specified) U 0
127905511 12790551 3 SS CARBOPLATIN. CARBOPLATIN 1 Intravenous (not otherwise specified) U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127905511 12790551 1 Endometrial cancer
127905511 12790551 2 Endometrial cancer
127905511 12790551 3 Endometrial cancer

Outcome of event

Event ID CASEID OUTC COD
127905511 12790551 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127905511 12790551 Anaemia
127905511 12790551 Blood bilirubin increased
127905511 12790551 Neutrophil count decreased
127905511 12790551 Proteinuria
127905511 12790551 White blood cell count decreased

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
127905511 12790551 1 20100202 0