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
121735342 12173534 2 F 2014 20160919 20160311 20160927 EXP FR-ASTRAZENECA-2016SE26251 ASTRAZENECA 74.00 YR F Y 0.00000 20160927 MD FR FR

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
121735342 12173534 1 PS IRESSA GEFITINIB 1 Oral Y U 206995 TABLET
121735342 12173534 2 SS IRESSA GEFITINIB 1 Oral Y U 206995 250 MG TABLET QOD
121735342 12173534 3 SS IRESSA GEFITINIB 1 Oral Y U 206995 250 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121735342 12173534 1 Non-small cell lung cancer recurrent
121735342 12173534 2 Non-small cell lung cancer recurrent
121735342 12173534 3 Non-small cell lung cancer recurrent

Outcome of event

Event ID CASEID OUTC COD
121735342 12173534 OT
121735342 12173534 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
121735342 12173534 Diarrhoea
121735342 12173534 Hepatitis
121735342 12173534 Malignant neoplasm progression
121735342 12173534 Neuropathy peripheral
121735342 12173534 Off label use
121735342 12173534 Toxic skin eruption

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
121735342 12173534 1 201408 0
121735342 12173534 2 201602 0