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
123049372 12304937 2 F 201508 20160624 20160426 20160706 EXP US-PFIZER INC-2015231705 PFIZER 73.00 YR M Y 70.31000 KG 20160706 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
123049372 12304937 1 PS SUTENT SUNITINIB MALATE 1 Oral 37.5 MG, 1X/DAY Y X731C 21938 37.5 MG CAPSULE, HARD QD
123049372 12304937 2 SS SUTENT SUNITINIB MALATE 1 Oral 37.5 MG, DAILY Y X731C 21938 37.5 MG CAPSULE, HARD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123049372 12304937 1 Chordoma

Outcome of event

Event ID CASEID OUTC COD
123049372 12304937 OT
123049372 12304937 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123049372 12304937 Ageusia
123049372 12304937 Atrial fibrillation
123049372 12304937 Chordoma
123049372 12304937 Disease progression
123049372 12304937 Dysphagia
123049372 12304937 Dyspnoea
123049372 12304937 Feeding disorder
123049372 12304937 Glossitis
123049372 12304937 Oral pain
123049372 12304937 Pharyngeal disorder
123049372 12304937 Pharyngeal inflammation
123049372 12304937 Pharyngeal ulceration
123049372 12304937 Product use issue
123049372 12304937 Pulmonary oedema
123049372 12304937 Stomatitis
123049372 12304937 Weight decreased

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
123049372 12304937 1 201507 20160401 0
123049372 12304937 2 20150720 20160404 0