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
120472528 12047252 8 F 20160228 20160719 20160209 20160727 EXP US-ASTRAZENECA-2015SE78238 ASTRAZENECA 26660.00 DY F Y 55.20000 KG 20160727 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
120472528 12047252 1 PS IRESSA GEFITINIB 1 Oral Y U 206995 TABLET
120472528 12047252 2 SS TAGRISSO OSIMERTINIB 1 Oral U U FN0072 0 80 MG TABLET QD
120472528 12047252 3 C ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 0
120472528 12047252 4 C PROAIR HFA ALBUTEROL SULFATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120472528 12047252 1 Metastases to lung
120472528 12047252 2 Lung carcinoma cell type unspecified stage 0

Outcome of event

Event ID CASEID OUTC COD
120472528 12047252 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
120472528 12047252 Decreased appetite
120472528 12047252 Diarrhoea
120472528 12047252 Disease progression
120472528 12047252 Drug dose omission
120472528 12047252 Dyspnoea
120472528 12047252 Fatigue
120472528 12047252 Muscle spasms
120472528 12047252 Nasopharyngitis
120472528 12047252 Nausea
120472528 12047252 Pruritus
120472528 12047252 Skin burning sensation
120472528 12047252 Skin exfoliation

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
120472528 12047252 2 20160205 0