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
124412352 12441235 2 F 20160520 20160627 20160607 20160705 EXP IN-PFIZER INC-2016025777 PFIZER 59.00 YR M Y 0.00000 20160705 CN IN IN

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
124412352 12441235 1 PS SUTENT SUNITINIB MALATE 1 Oral 50 MG, 1X/DAY 21938 50 MG CAPSULE, HARD QD
124412352 12441235 2 SS SUTENT SUNITINIB MALATE 1 Oral 50 MG, 1X/DAY 21938 50 MG CAPSULE, HARD QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124412352 12441235 1 Gastrointestinal stromal tumour

Outcome of event

Event ID CASEID OUTC COD
124412352 12441235 DE
124412352 12441235 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124412352 12441235 Asthenia
124412352 12441235 Blood pressure abnormal
124412352 12441235 Body temperature decreased
124412352 12441235 Death
124412352 12441235 Dysarthria
124412352 12441235 Fall
124412352 12441235 Haemoglobin decreased
124412352 12441235 Heart rate decreased
124412352 12441235 Liver function test abnormal
124412352 12441235 Skin disorder
124412352 12441235 Urinary retention

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
124412352 12441235 1 20120312 201407 0
124412352 12441235 2 201601 20160526 0