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
113711514 11371151 4 F 2012 20160826 20150812 20160906 EXP US-PFIZER INC-2015256015 PFIZER 62.00 YR M Y 115.20000 KG 20160906 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
113711514 11371151 1 PS SUTENT SUNITINIB MALATE 1 Oral 20 OR 25 MG, CYCLIC (21 DAYS ON 14 DAYS OFF) Y 21938 CAPSULE, HARD
113711514 11371151 2 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 40 MG, UNK 0 40 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113711514 11371151 1 Renal cell carcinoma

Outcome of event

Event ID CASEID OUTC COD
113711514 11371151 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
113711514 11371151 Cough
113711514 11371151 Dehydration
113711514 11371151 Diarrhoea
113711514 11371151 Disease progression
113711514 11371151 Oral pain
113711514 11371151 Pharyngeal disorder
113711514 11371151 Renal cell carcinoma
113711514 11371151 Thrombosis

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
113711514 11371151 1 201112 2013 0