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
112613222 11261322 2 F 20150630 20160923 20150710 20160930 EXP ES-ASTELLAS-2015US024261 ASTELLAS 49.92 YR F Y 0.00000 20160930 CN GB ES

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
112613222 11261322 1 PS Erlotinib ERLOTINIB 1 Oral U 21743 150 MG TABLET QD
112613222 11261322 2 SS Erlotinib ERLOTINIB 1 Oral U 21743 100 MG TABLET QD
112613222 11261322 3 SS Erlotinib ERLOTINIB 1 Oral U 21743 100 MG TABLET QD
112613222 11261322 4 SS BEVACIZUMAB BEVACIZUMAB 1 Intravenous (not otherwise specified) 1218 MG, ON DAY 1 OF 21 DAY CYCLE Y 0 1218 MG FORMULATION UNKNOWN
112613222 11261322 5 C SUTRIL /01036501/ TORSEMIDE 1 Oral D U 0 5 MG FORMULATION UNKNOWN
112613222 11261322 6 C ENALAPRIL ENALAPRIL 1 Oral 10, UNKNOWN FREQ. D U 0 FORMULATION UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
112613222 11261322 1 Non-small cell lung cancer
112613222 11261322 4 Non-small cell lung cancer
112613222 11261322 5 Product used for unknown indication
112613222 11261322 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
112613222 11261322 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
112613222 11261322 Hypertension

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
112613222 11261322 1 20130613 0
112613222 11261322 2 20150629 0
112613222 11261322 3 20160830 0
112613222 11261322 4 20130613 0
112613222 11261322 5 20150630 0
112613222 11261322 6 20160831 0