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
113262052 11326205 2 F 20140911 20160706 20150731 20160713 EXP PHHY2014JP148707 NOVARTIS 68.19 YR F Y 38.00000 KG 20160713 OT 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
113262052 11326205 1 PS AFINITOR EVEROLIMUS 1 Oral 10 MG, QD 500 MG 22334 10 MG QD
113262052 11326205 2 C AROMASIN EXEMESTANE 1 Oral 25 MG, QD 0 25 MG QD
113262052 11326205 3 C EXEMESTANE. EXEMESTANE 1 Oral 25 MG, QD 0 25 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113262052 11326205 1 Breast cancer recurrent
113262052 11326205 2 Product used for unknown indication
113262052 11326205 3 Breast cancer recurrent

Outcome of event

Event ID CASEID OUTC COD
113262052 11326205 OT
113262052 11326205 LT
113262052 11326205 HO
113262052 11326205 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
113262052 11326205 Anaemia
113262052 11326205 Cough
113262052 11326205 Dysphonia
113262052 11326205 Dyspnoea
113262052 11326205 Interstitial lung disease
113262052 11326205 Platelet count decreased
113262052 11326205 Pleural effusion
113262052 11326205 Productive cough
113262052 11326205 Respiratory failure
113262052 11326205 Stomatitis
113262052 11326205 Suffocation feeling

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
113262052 11326205 1 20140908 20141027 0
113262052 11326205 2 20141027 0
113262052 11326205 3 20140908 0