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
127829001 12782900 1 I 20160823 20160927 20160927 EXP US-ROCHE-1833840 ROCHE 60.00 YR F Y 58.80000 KG 20160927 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
127829001 12782900 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) CYCLE 1 U 125085
127829001 12782900 2 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) CYCLE 2 U 125085 969 MG
127829001 12782900 3 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) CYCLE 3 U 125085
127829001 12782900 4 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) CYCLE 4 U 125085
127829001 12782900 5 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) CYCLE 5 U 125085
127829001 12782900 6 SS IXABEPILONE IXABEPILONE 1 Intravenous (not otherwise specified) CYCLE 1 U 0 52.8 MG
127829001 12782900 7 SS IXABEPILONE IXABEPILONE 1 Intravenous (not otherwise specified) CYCLE 2 U 0 54.6 MG
127829001 12782900 8 SS IXABEPILONE IXABEPILONE 1 Intravenous (not otherwise specified) CYCLE 3 U 0 54.6 MG
127829001 12782900 9 SS IXABEPILONE IXABEPILONE 1 Intravenous (not otherwise specified) CYCLE 4 U 0 54.6 MG
127829001 12782900 10 SS IXABEPILONE IXABEPILONE 1 Intravenous (not otherwise specified) CYCLE 5 U 0 54.6 MG
127829001 12782900 11 SS CARBOPLATIN. CARBOPLATIN 1 Intravenous (not otherwise specified) U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127829001 12782900 1 Papillary serous endometrial carcinoma
127829001 12782900 6 Papillary serous endometrial carcinoma
127829001 12782900 11 Papillary serous endometrial carcinoma

Outcome of event

Event ID CASEID OUTC COD
127829001 12782900 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127829001 12782900 Anaemia
127829001 12782900 Neutrophil count decreased
127829001 12782900 Platelet count decreased
127829001 12782900 Urinary anastomotic leak
127829001 12782900 Vaginal fistula
127829001 12782900 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
127829001 12782900 1 20101104 0
127829001 12782900 2 20101129 0
127829001 12782900 3 20110106 0
127829001 12782900 4 20110127 0
127829001 12782900 5 20110309 0
127829001 12782900 6 20101104 0
127829001 12782900 7 20101129 0
127829001 12782900 8 20110106 0
127829001 12782900 9 20110127 0
127829001 12782900 10 20110309 0