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
123318982 12331898 2 F 20160420 20160726 20160504 20160808 EXP US-PFIZER INC-2016127943 PFIZER 67.00 YR M Y 0.00000 20160808 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
123318982 12331898 1 PS SUTENT SUNITINIB MALATE 1 Oral 50 MG, 1X/DAY 21938 50 MG CAPSULE, HARD QD
123318982 12331898 2 C FLUTICASONE FLUTICASONEFLUTICASONE PROPIONATE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123318982 12331898 1 Metastatic renal cell carcinoma

Outcome of event

Event ID CASEID OUTC COD
123318982 12331898 DE
123318982 12331898 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123318982 12331898 Deafness
123318982 12331898 Death
123318982 12331898 Ear disorder

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
123318982 12331898 1 201603 0
123318982 12331898 2 20160420 20160509 0