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
127882961 12788296 1 I 20160826 20160914 20160928 20160928 EXP IT-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-124500 RANBAXY 45.63 YR F Y 48.00000 KG 20160928 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
127882961 12788296 1 PS GEMCITABINE GEMCITABINEGEMCITABINE HYDROCHLORIDE 1 Intravenous drip 1480 MG CYCLICAL U U 78433 1480 MG
127882961 12788296 2 SS ABRAXANE PACLITAXEL 1 Intravenous drip 185 MG CYCLICAL U U 0 185 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127882961 12788296 1 Pancreatic carcinoma
127882961 12788296 2 Pancreatic carcinoma

Outcome of event

Event ID CASEID OUTC COD
127882961 12788296 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127882961 12788296 Enteritis
127882961 12788296 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
127882961 12788296 1 20160601 0
127882961 12788296 2 20160601 0