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
116766116 11676611 6 F 2015 20160816 20151028 20160826 EXP US-PFIZER INC-2015309073 PFIZER 55.00 YR M Y 75.28000 KG 20160826 OT 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
116766116 11676611 1 PS SUTENT SUNITINIB MALATE 1 Oral 37.5 MG ONCE DAILY, CYCLIC (DAYS 1-28 Q 28 DAYS) N X731C 21938 37.5 MG CAPSULE, HARD
116766116 11676611 2 SS SUTENT SUNITINIB MALATE 1 UNK N 440CB 21938 CAPSULE, HARD
116766116 11676611 3 SS SUTENT SUNITINIB MALATE 1 UNK N X731B 21938 CAPSULE, HARD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116766116 11676611 1 Carcinoid tumour

Outcome of event

Event ID CASEID OUTC COD
116766116 11676611 OT
116766116 11676611 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
116766116 11676611 Abdominal pain
116766116 11676611 Blood pressure increased
116766116 11676611 Carcinoid tumour
116766116 11676611 Cholecystitis
116766116 11676611 Disease progression
116766116 11676611 Insomnia
116766116 11676611 Malaise
116766116 11676611 Nausea
116766116 11676611 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
116766116 11676611 1 20150811 0