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
107588297 10758829 7 F 20140721 20160719 20150203 20160805 PER US-PFIZER INC-2015035591 PFIZER 74.00 YR M Y 81.63000 KG 20160805 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
107588297 10758829 1 PS SUTENT SUNITINIB MALATE 1 Oral 37.5 MG DAILY FOR 4 WEEKS ON/ 2 WEEKS OFF N X731B 21938 37.5 MG CAPSULE, HARD
107588297 10758829 2 SS SUTENT SUNITINIB MALATE 1 Oral 37.5 MG, DAILY N 258CA 21938 37.5 MG CAPSULE, HARD
107588297 10758829 3 SS SUTENT SUNITINIB MALATE 1 Oral 37.5 MG, CYCLIC (DAYS 1-28 Q42 DAYS) N 258CA 21938 37.5 MG CAPSULE, HARD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
107588297 10758829 1 Gastrointestinal stromal tumour

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
107588297 10758829 Arthralgia
107588297 10758829 Diarrhoea
107588297 10758829 Disease progression
107588297 10758829 Drug dose omission
107588297 10758829 Dry mouth
107588297 10758829 Dry skin
107588297 10758829 Fatigue
107588297 10758829 Gastrointestinal stromal tumour
107588297 10758829 Paranasal sinus hypersecretion
107588297 10758829 Sinus congestion

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
107588297 10758829 1 20140620 0
107588297 10758829 2 20140611 0
107588297 10758829 3 20140611 0