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
90576133 9057613 3 F 20130114 20130204 20160902 EXP IE-PFIZER INC-2013043743 PFIZER 0.00 M Y 0.00000 20160902 CN IE IE

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
90576133 9057613 1 PS SUTENT SUNITINIB MALATE 1 50 MG, 1X/DAY U 21938 50 MG CAPSULE, HARD QD
90576133 9057613 2 SS SUTENT SUNITINIB MALATE 1 50, CYCLIC (4/2 AS PRODUCT SCHEDULE ) U 21938 CAPSULE, HARD
90576133 9057613 3 SS SUTENT SUNITINIB MALATE 1 37.5, CYCLIC (4/2 AS PRODUCT SCHEDULE ) U 21938 CAPSULE, HARD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
90576133 9057613 1 Metastatic renal cell carcinoma

Outcome of event

Event ID CASEID OUTC COD
90576133 9057613 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
90576133 9057613 Decreased appetite
90576133 9057613 Decubitus ulcer
90576133 9057613 Fatigue
90576133 9057613 Lethargy
90576133 9057613 Oedema peripheral
90576133 9057613 Pallor
90576133 9057613 Palmar-plantar erythrodysaesthesia syndrome
90576133 9057613 Retching
90576133 9057613 Stomatitis
90576133 9057613 Vomiting

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
90576133 9057613 1 20120107 0
90576133 9057613 2 20130107 0
90576133 9057613 3 20130424 0