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
124697182 12469718 2 F 2015 20160629 20160615 20160707 EXP CN-ASTRAZENECA-2016SE64463 ASTRAZENECA 78.00 YR F Y 0.00000 20160707 CN CN CN

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
124697182 12469718 1 PS IRESSA GEFITINIB 1 Oral 518 DF Y U 206995 1 DF TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124697182 12469718 1 Small cell lung cancer

Outcome of event

Event ID CASEID OUTC COD
124697182 12469718 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124697182 12469718 Cerebral atrophy
124697182 12469718 Cerebral calcification
124697182 12469718 Chest discomfort
124697182 12469718 Decreased appetite
124697182 12469718 Dizziness
124697182 12469718 Gait disturbance
124697182 12469718 Head discomfort
124697182 12469718 Hiccups
124697182 12469718 Language disorder
124697182 12469718 Loss of consciousness
124697182 12469718 Rash pruritic
124697182 12469718 Tension headache
124697182 12469718 Vomiting

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
124697182 12469718 1 201411 201604 0