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
122472862 12247286 2 F 2016 20160727 20160407 20160809 EXP US-PFIZER INC-2016179779 PFIZER 61.00 YR M Y 86.00000 KG 20160809 PH 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
122472862 12247286 1 PS SUTENT SUNITINIB MALATE 1 Oral 50 MG, CYCLIC (DAILY D1-D25 Q42 D) Y 21938 50 MG CAPSULE, HARD
122472862 12247286 2 SS SUTENT SUNITINIB MALATE 1 Oral 50 MG, CYCLIC (DAILY X 4 WKS THEN 2 WKS) Y 595BA 21938 50 MG CAPSULE, HARD
122472862 12247286 3 SS SUTENT SUNITINIB MALATE 1 Oral 50 MG, CYCLIC (D1-D28 Q42 D) Y 595BA 21938 50 MG CAPSULE, HARD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122472862 12247286 1 Renal cancer

Outcome of event

Event ID CASEID OUTC COD
122472862 12247286 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
122472862 12247286 Abdominal discomfort
122472862 12247286 Abdominal distension
122472862 12247286 Abdominal pain upper
122472862 12247286 Ageusia
122472862 12247286 Asthenia
122472862 12247286 Blood pressure increased
122472862 12247286 Diarrhoea
122472862 12247286 Dysgeusia
122472862 12247286 Dyspepsia
122472862 12247286 Fatigue
122472862 12247286 Headache
122472862 12247286 Pleural effusion
122472862 12247286 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
122472862 12247286 1 20160212 0
122472862 12247286 2 20160323 20160726 0
122472862 12247286 3 20160212 20160629 0