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
126498311 12649831 1 I 20160803 20160812 20160812 EXP JP-ASTRAZENECA-2016SE85783 ASTRAZENECA 60.00 YR M Y 0.00000 20160813 MD JP JP

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
126498311 12649831 1 PS IRESSA GEFITINIB 1 Oral Y U 206995 250 MG TABLET QD
126498311 12649831 2 SS IRESSA GEFITINIB 1 Oral Y U 206995 250 MG TABLET QD
126498311 12649831 3 C ALIMTA PEMETREXED DISODIUM 1 Unknown DOSE UNKNOWN 0
126498311 12649831 4 C AVASTIN BEVACIZUMAB 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126498311 12649831 1 Non-small cell lung cancer
126498311 12649831 2 Non-small cell lung cancer
126498311 12649831 3 Non-small cell lung cancer
126498311 12649831 4 Non-small cell lung cancer

Outcome of event

Event ID CASEID OUTC COD
126498311 12649831 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126498311 12649831 Malignant neoplasm progression
126498311 12649831 Rash

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found