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
126985812 12698581 2 F 201403 20160818 20160830 20160906 EXP CO-ASTRAZENECA-2016SE35998 ASTRAZENECA 819.00 MON F Y 50.00000 KG 20160906 CO CO

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
126985812 12698581 1 PS IRESSA GEFITINIB 1 Oral 0 250 MG TABLET QD
126985812 12698581 2 SS IRESSA GEFITINIB 1 Oral 0 250 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126985812 12698581 1 Lung neoplasm malignant
126985812 12698581 2 Lung neoplasm malignant

Outcome of event

Event ID CASEID OUTC COD
126985812 12698581 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126985812 12698581 Arthralgia
126985812 12698581 Chest pain
126985812 12698581 Decreased appetite
126985812 12698581 Depression
126985812 12698581 Drug dose omission
126985812 12698581 Dyspnoea
126985812 12698581 Malignant neoplasm progression
126985812 12698581 Soft tissue disorder
126985812 12698581 Urinary tract infection

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
126985812 12698581 1 20130401 0
126985812 12698581 2 201605 0