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
125651261 12565126 1 I 20100312 20100406 20160718 20160718 EXP US-ROCHE-697850 ROCHE 37.00 YR F Y 75.50000 KG 20160718 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
125651261 12565126 1 PS Erlotinib ERLOTINIB 1 Oral U 53728 75 MG
125651261 12565126 2 SS Vismodegib VISMODEGIB 1 Oral U 203388 150 MG
125651261 12565126 3 SS GEMCITABINE GEMCITABINEGEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) U 0 1000 MG/M**2

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125651261 12565126 1 Pancreatic carcinoma
125651261 12565126 2 Pancreatic carcinoma
125651261 12565126 3 Pancreatic carcinoma

Outcome of event

Event ID CASEID OUTC COD
125651261 12565126 OT
125651261 12565126 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125651261 12565126 Dyspnoea
125651261 12565126 Embolism
125651261 12565126 Hypoxia
125651261 12565126 Platelet count decreased
125651261 12565126 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
125651261 12565126 1 20100219 20100313 0
125651261 12565126 2 20100219 20100313 0
125651261 12565126 3 20100219 20100313 0