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
126641951 12664195 1 I 20100618 20100707 20160818 20160818 EXP US-ASTELLAS-2010002766 ASTELLAS 66.97 YR M Y 0.00000 20160818 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
126641951 12664195 1 PS Erlotinib ERLOTINIB 1 Oral U 21743 100 MG TABLET QD
126641951 12664195 2 SS Erlotinib ERLOTINIB 1 Oral 21743 75 MG TABLET QD
126641951 12664195 3 SS VISMODEGIB VISMODEGIB 1 Oral U 0 150 MG CAPSULE QD
126641951 12664195 4 SS VISMODEGIB VISMODEGIB 1 0 CAPSULE
126641951 12664195 5 SS GEMCITABINE GEMCITABINEGEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) 1000 MG/M2, DAYS 1, 8, 15 (3 IN I CYCLE) U 0 1000 MG/M**2 FORMULATION UNKNOWN
126641951 12664195 6 C DILTIAZEM. DILTIAZEM 1 Unknown UNK, UNKNOWN FREQ. U 0 FORMULATION UNKNOWN
126641951 12664195 7 C LOVASTATIN. LOVASTATIN 1 Unknown UNK, UNKNOWN FREQ. U 0 FORMULATION UNKNOWN
126641951 12664195 8 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Unknown UNK, UNKNOWN FREQ. U 0 FORMULATION UNKNOWN
126641951 12664195 9 C PROPAFENONE. PROPAFENONE 1 Unknown UNK, UNKNOWN FREQ. U 0 FORMULATION UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126641951 12664195 1 Pancreatic carcinoma
126641951 12664195 2 Adenocarcinoma pancreas
126641951 12664195 3 Pancreatic carcinoma
126641951 12664195 4 Adenocarcinoma pancreas
126641951 12664195 5 Pancreatic carcinoma
126641951 12664195 6 Product used for unknown indication
126641951 12664195 7 Product used for unknown indication
126641951 12664195 8 Product used for unknown indication
126641951 12664195 9 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126641951 12664195 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126641951 12664195 Decreased appetite
126641951 12664195 Dehydration
126641951 12664195 Diarrhoea
126641951 12664195 Fatigue
126641951 12664195 Hypokalaemia
126641951 12664195 Hyponatraemia
126641951 12664195 Lung infection
126641951 12664195 Nausea
126641951 12664195 Non-cardiac chest pain
126641951 12664195 Pneumonia
126641951 12664195 Pyrexia

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
126641951 12664195 1 20100511 0
126641951 12664195 3 20100511 0
126641951 12664195 5 20100511 0