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
127303771 12730377 1 I 201607 20160901 20160909 20160909 EXP FR-ASTRAZENECA-2016SE95002 ASTRAZENECA 77.00 YR M Y 0.00000 20160909 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
127303771 12730377 1 PS IRESSA GEFITINIB 1 Oral 68750 MG N U 206995 250 MG TABLET QD
127303771 12730377 2 SS IRESSA GEFITINIB 1 Oral 68750 MG N U 206995 250 MG TABLET QD
127303771 12730377 3 SS TAGRISSO OSIMERTINIB 1 Oral 4880 MG N U 0 80 MG TABLET QD
127303771 12730377 4 C RADIOTHERAPY RADIATION THERAPY 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127303771 12730377 1 Bronchial carcinoma
127303771 12730377 2 Bronchial carcinoma
127303771 12730377 3 Bronchial carcinoma

Outcome of event

Event ID CASEID OUTC COD
127303771 12730377 HO
127303771 12730377 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127303771 12730377 Encephalopathy
127303771 12730377 Malignant neoplasm progression
127303771 12730377 Metastases to central nervous system
127303771 12730377 Radiation injury

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
127303771 12730377 1 201506 201507 0
127303771 12730377 2 20150910 201605 0
127303771 12730377 3 201605 201608 0