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
108870163 10887016 3 F 20160627 20150304 20160707 PER US-PFIZER INC-2015076555 PFIZER 67.00 YR M Y 0.00000 20160707 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
108870163 10887016 1 PS SUTENT SUNITINIB MALATE 1 50 MG, UNK 21938 50 MG CAPSULE, HARD
108870163 10887016 2 SS SUTENT SUNITINIB MALATE 1 37.5 MG, UNK 21938 37.5 MG CAPSULE, HARD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
108870163 10887016 1 Gastric cancer

Outcome of event

Event ID CASEID OUTC COD
108870163 10887016 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
108870163 10887016 Abdominal discomfort
108870163 10887016 Asthenia
108870163 10887016 Cough
108870163 10887016 Decreased appetite
108870163 10887016 Diarrhoea
108870163 10887016 Dysgeusia
108870163 10887016 Dyspnoea
108870163 10887016 Epistaxis
108870163 10887016 Fatigue
108870163 10887016 Flatulence
108870163 10887016 Nausea
108870163 10887016 Peripheral swelling
108870163 10887016 Rash
108870163 10887016 Renal impairment
108870163 10887016 Retching
108870163 10887016 Skin irritation
108870163 10887016 Stomatitis

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
108870163 10887016 1 2007 0
108870163 10887016 2 2007 201501 0