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
126794171 12679417 1 I 20040302 20160824 20160824 PER US-ASTRAZENECA-2004UW03846 ASTRAZENECA 40.00 YR F Y 72.60000 KG 20160824 CN US US

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
126794171 12679417 1 PS IRESSA GEFITINIB 1 Oral 206995 250 MG TABLET QD
126794171 12679417 2 C COUMADIN WARFARIN SODIUM 1 0
126794171 12679417 3 C PREVACID LANSOPRAZOLE 1 0
126794171 12679417 4 C OXYCONTIN OXYCODONE HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126794171 12679417 1 Non-small cell lung cancer

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126794171 12679417 Dermatitis acneiform
126794171 12679417 Diarrhoea
126794171 12679417 Dizziness
126794171 12679417 Gastrooesophageal reflux disease
126794171 12679417 Hepatic enzyme increased
126794171 12679417 Nausea

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
126794171 12679417 1 200305 0