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
118050682 11805068 2 F 20160711 20151206 20160902 PER US-ASTRAZENECA-2015SF19043 ASTRAZENECA 0.00 M Y 109.80000 KG 20160902 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
118050682 11805068 1 PS IRESSA GEFITINIB 1 Oral 206995 250 MG TABLET QD
118050682 11805068 2 SS IRESSA GEFITINIB 1 Oral 206995 250 MG TABLET QD
118050682 11805068 3 SS IRESSA GEFITINIB 1 Oral 206995 250 MG TABLET QOD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118050682 11805068 1 Lung neoplasm malignant
118050682 11805068 2 Lung neoplasm malignant
118050682 11805068 3 Lung neoplasm malignant

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
118050682 11805068 Acne
118050682 11805068 Alopecia
118050682 11805068 Epistaxis
118050682 11805068 Hair texture abnormal
118050682 11805068 Rash pruritic

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
118050682 11805068 1 20151010 0
118050682 11805068 2 20151016 201511 0
118050682 11805068 3 201511 0