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
126396962 12639696 2 F 2016 20160808 20160810 20160816 EXP RU-ASTRAZENECA-2016SE85274 ASTRAZENECA 72.00 YR F Y 0.00000 20160817 MD RU RU

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
126396962 12639696 1 PS IRESSA GEFITINIB 1 Oral 164550 MG N U 206995 150 MG TABLET QD
126396962 12639696 2 SS IRESSA GEFITINIB 1 Oral 164550 MG N U 206995 250 MG TABLET QD
126396962 12639696 3 C BIPHOSPHONATE 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126396962 12639696 1 Lung adenocarcinoma
126396962 12639696 2 Lung adenocarcinoma

Outcome of event

Event ID CASEID OUTC COD
126396962 12639696 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126396962 12639696 Malignant neoplasm progression
126396962 12639696 Metastases to bone
126396962 12639696 Metastases to lung

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
126396962 12639696 1 20150319 201607 0
126396962 12639696 2 20150318 201607 0