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
127892942 12789294 2 F 20160826 20160920 20160928 20160930 EXP IT-MINISAL02-374645 IT-TEVA-694725ACC TEVA 45.63 YR F Y 48.00000 KG 20160930 PH 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
127892942 12789294 1 PS GEMCITABINE GEMCITABINEGEMCITABINE HYDROCHLORIDE 1 Intravenous drip 1480 MG CYCLICAL U 0 1480 MG SOLUTION FOR INFUSION
127892942 12789294 2 SS ABRAXANE PACLITAXEL 1 Intravenous drip 185 MG CYCLICAL U 0 185 MG SOLUTION FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127892942 12789294 1 Pancreatic carcinoma
127892942 12789294 2 Pancreatic carcinoma

Outcome of event

Event ID CASEID OUTC COD
127892942 12789294 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127892942 12789294 Enteritis
127892942 12789294 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
127892942 12789294 1 20160601 0
127892942 12789294 2 20160601 0