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
123976414 12397641 4 F 20160415 20160811 20160524 20160816 EXP PHHY2016PH070378 NOVARTIS 52.26 YR F Y 0.00000 20160816 MD PH PH

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
123976414 12397641 1 PS AFINITOR EVEROLIMUS 1 Oral 10 MG, QD 120 MG 22334 10 MG QD
123976414 12397641 2 SS AFINITOR EVEROLIMUS 1 Oral 5 MG, QOD 120 MG 22334 5 MG
123976414 12397641 3 SS AFINITOR EVEROLIMUS 1 Oral 10 MG, QD 120 MG 22334 10 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123976414 12397641 1 Breast cancer

Outcome of event

Event ID CASEID OUTC COD
123976414 12397641 OT
123976414 12397641 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123976414 12397641 Acute kidney injury
123976414 12397641 Asthenia
123976414 12397641 Chest discomfort
123976414 12397641 Cough
123976414 12397641 Decreased appetite
123976414 12397641 Dysuria
123976414 12397641 Fatigue
123976414 12397641 Nausea
123976414 12397641 Pleural effusion
123976414 12397641 Pulmonary oedema
123976414 12397641 Urinary tract infection

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
123976414 12397641 1 20160405 20160416 0
123976414 12397641 2 20160515 20160612 0
123976414 12397641 3 20160612 0