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
89235192 8923519 2 F 20130125 20121123 20160921 EXP IE-PFIZER INC-2012290578 PFIZER 0.00 M Y 0.00000 20160921 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
89235192 8923519 1 PS SUTENT SUNITINIB MALATE 1 50 MG, CYCLIC (ON 4/2 SCHEDULE) Y 21938 50 MG CAPSULE, HARD
89235192 8923519 2 SS SUTENT SUNITINIB MALATE 1 37.5 MG, CYCLIC (1X/DAY,4 WEEKS ON 2 WEEKS OFF ) Y 21938 37.5 MG CAPSULE, HARD
89235192 8923519 3 C DEXAMETHASONE. DEXAMETHASONE 1 8 MG, DAILY 0 8 MG
89235192 8923519 4 C DEXAMETHASONE. DEXAMETHASONE 1 2 MG, DAILY 0 2 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
89235192 8923519 1 Renal cancer metastatic

Outcome of event

Event ID CASEID OUTC COD
89235192 8923519 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
89235192 8923519 Anaemia
89235192 8923519 Disease progression
89235192 8923519 Dyspnoea
89235192 8923519 Excoriation
89235192 8923519 Fatigue
89235192 8923519 Haemorrhoidal haemorrhage
89235192 8923519 Hypertension
89235192 8923519 Influenza
89235192 8923519 Oral pain
89235192 8923519 Proteinuria
89235192 8923519 Renal cancer metastatic
89235192 8923519 Sepsis
89235192 8923519 Tumour pain

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
89235192 8923519 1 20120910 0
89235192 8923519 2 20130125 0