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
113648694 11364869 4 F 20150715 20160629 20150811 20160711 EXP CN-PFIZER INC-2015250823 PFIZER 69.00 YR M Y 0.00000 20160711 CN CN CN

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
113648694 11364869 1 PS SUTENT SUNITINIB MALATE 1 UNK 21938 CAPSULE, HARD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113648694 11364869 1 Gastrointestinal stromal tumour

Outcome of event

Event ID CASEID OUTC COD
113648694 11364869 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
113648694 11364869 Anal ulcer
113648694 11364869 Disease progression
113648694 11364869 Gastrointestinal stromal tumour
113648694 11364869 Mouth ulceration
113648694 11364869 Oedema peripheral

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found