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
127907631 12790763 1 I 20160823 20160929 20160929 EXP US-ROCHE-1835021 ROCHE 73.00 YR F Y 73.60000 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
127907631 12790763 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) LAST TREATMENT RECEIVED ON 02/MAY/2012 U 125085 1105 MG
127907631 12790763 2 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) U 125085 1105 MG
127907631 12790763 3 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) U 125085 1105 MG
127907631 12790763 4 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) U 125085 1105 MG
127907631 12790763 5 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) U 125085 1105 MG
127907631 12790763 6 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) U 125085 965 MG
127907631 12790763 7 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) U 125085 965 MG
127907631 12790763 8 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) U 125085 965 MG
127907631 12790763 9 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) U 125085 965 MG
127907631 12790763 10 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) U 125085 835 MG
127907631 12790763 11 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) U 125085 835 MG
127907631 12790763 12 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) U 125085 835 MG
127907631 12790763 13 SS PACLITAXEL. PACLITAXEL 1 Intravenous (not otherwise specified) U 0
127907631 12790763 14 SS CARBOPLATIN. CARBOPLATIN 1 Intravenous (not otherwise specified) U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127907631 12790763 1 Endometrial cancer
127907631 12790763 13 Endometrial cancer
127907631 12790763 14 Endometrial cancer

Outcome of event

Event ID CASEID OUTC COD
127907631 12790763 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127907631 12790763 Blood bilirubin increased
127907631 12790763 Neutrophil count decreased
127907631 12790763 Peripheral motor neuropathy
127907631 12790763 Peripheral sensory neuropathy
127907631 12790763 Platelet count decreased
127907631 12790763 Weight decreased
127907631 12790763 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
127907631 12790763 1 20110823 0
127907631 12790763 2 20110913 0
127907631 12790763 3 20111004 0
127907631 12790763 4 20111101 0
127907631 12790763 5 20111128 0
127907631 12790763 6 20111228 0
127907631 12790763 7 20120117 0
127907631 12790763 8 20120207 0
127907631 12790763 9 20120228 0
127907631 12790763 10 20120320 0
127907631 12790763 11 20120410 0
127907631 12790763 12 20120502 0