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
125478582 12547858 2 F 20160606 20160708 20160712 20160716 EXP JP-ASTRAZENECA-2016SE65058 ASTRAZENECA 70.00 YR F Y 59.00000 KG 20160716 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
125478582 12547858 1 PS TAGRISSO OSIMERTINIB 1 Oral Y U 0 80 MG TABLET QD
125478582 12547858 2 SS TAGRISSO OSIMERTINIB 1 Oral Y U 0 80 MG TABLET QD
125478582 12547858 3 SS CARBOCISTEINE CARBOCYSTEINE 1 Unknown 7500 MG U U 0 1500 MG QD
125478582 12547858 4 SS AMBROXOL HYDROCHLORIDE AMBROXOL HYDROCHLORIDE 1 Unknown 225 MG U U 0 45 MG QD
125478582 12547858 5 SS LOXONIN LOXOPROFEN SODIUM 1 Unknown 6540 MG U U 0 60 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125478582 12547858 1 Non-small cell lung cancer
125478582 12547858 2 Non-small cell lung cancer
125478582 12547858 3 Productive cough
125478582 12547858 4 Productive cough
125478582 12547858 5 Analgesic therapy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125478582 12547858 Adjustment disorder
125478582 12547858 Diarrhoea
125478582 12547858 Erythema
125478582 12547858 Nausea
125478582 12547858 Pruritus
125478582 12547858 Rash

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
125478582 12547858 1 20160603 20160630 0
125478582 12547858 2 20160705 0
125478582 12547858 3 20160602 0
125478582 12547858 4 20160602 0
125478582 12547858 5 20160219 0