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
120006915 12000691 5 F 20160129 20160725 20160204 20160804 PER US-PFIZER INC-2016058064 PFIZER 85.00 YR M Y 82.00000 KG 20160804 OT 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
120006915 12000691 1 PS SUTENT SUNITINIB MALATE 1 Oral 37.5 MG, 1X/DAY Y X731C 21938 37.5 MG CAPSULE, HARD QD
120006915 12000691 2 SS SUTENT SUNITINIB MALATE 1 Oral 37.5 MG, 1X/DAY Y X731C 21938 37.5 MG CAPSULE, HARD QD
120006915 12000691 3 SS SUTENT SUNITINIB MALATE 1 Oral 25 MG, CYCLIC (DAY 1-28Q 28 DAYS) Y 684BA 21938 25 MG CAPSULE, HARD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120006915 12000691 1 Renal cancer

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
120006915 12000691 Abdominal discomfort
120006915 12000691 Ageusia
120006915 12000691 Asthenia
120006915 12000691 Constipation
120006915 12000691 Decreased appetite
120006915 12000691 Diarrhoea
120006915 12000691 Dysgeusia
120006915 12000691 Weight decreased

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
120006915 12000691 1 20151219 0
120006915 12000691 3 20160317 0