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
125797421 12579742 1 I 20100312 20100406 20160721 20160721 EXP US-ASTELLAS-2010001262 ASTELLAS 37.00 YR F Y 0.00000 20160721 OT 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
125797421 12579742 1 PS Erlotinib ERLOTINIB 1 Oral U 21743 75 MG TABLET QD
125797421 12579742 2 SS VISMODEGIB VISMODEGIB 1 Oral U 0 150 MG FORMULATION UNKNOWN QD
125797421 12579742 3 SS GEMCITABINE GEMCITABINEGEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) U 0 1000 MG/M**2 FORMULATION UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125797421 12579742 1 Pancreatic carcinoma
125797421 12579742 2 Pancreatic carcinoma
125797421 12579742 3 Pancreatic carcinoma

Outcome of event

Event ID CASEID OUTC COD
125797421 12579742 OT
125797421 12579742 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125797421 12579742 Dyspnoea
125797421 12579742 Embolism
125797421 12579742 Hypoxia
125797421 12579742 Platelet count decreased
125797421 12579742 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
125797421 12579742 1 20100219 20100313 0
125797421 12579742 2 20100219 20100313 0
125797421 12579742 3 20100219 20100313 0