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
127708141 12770814 1 I 20160807 20160907 20160922 20160922 EXP IT-CELGENEUS-ITA-2016091442 CELGENE 45.00 YR F Y 48.00000 KG 20160922 OT IT IT

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
127708141 12770814 1 PS ABRAXANE PACLITAXEL 1 Intravenous drip Y U L01CD01 21660 150 MG INJECTION FOR INFUSION
127708141 12770814 2 SS ABRAXANE PACLITAXEL 1 Intravenous drip Y U L01CD01 21660 185 MG INJECTION FOR INFUSION
127708141 12770814 3 SS GEMCITABINE GEMCITABINEGEMCITABINE HYDROCHLORIDE 1 Intravenous drip Y U L01BC05 55974 1200 MG SOLUTION
127708141 12770814 4 SS GEMCITABINE GEMCITABINEGEMCITABINE HYDROCHLORIDE 1 Intravenous drip Y U L01BC05 55974 1480 MG SOLUTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127708141 12770814 1 Pancreatic carcinoma
127708141 12770814 3 Pancreatic carcinoma

Outcome of event

Event ID CASEID OUTC COD
127708141 12770814 HO
127708141 12770814 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127708141 12770814 Enteritis
127708141 12770814 Haematotoxicity
127708141 12770814 Pancytopenia

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
127708141 12770814 1 20160826 0
127708141 12770814 2 20160601 20160811 0
127708141 12770814 3 20160826 0
127708141 12770814 4 20160601 20160811 0