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
114319193 11431919 3 F 20160913 20150828 20160919 PER US-PFIZER INC-2015274043 PFIZER 45.00 YR M Y 88.89000 KG 20160919 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
114319193 11431919 1 PS SUTENT SUNITINIB MALATE 1 Oral 50 MG, CYCLIC (FOR DAY 1 TO DAY 14 EVERY 21 DAYS) Y 21938 50 MG CAPSULE, HARD
114319193 11431919 2 SS SUTENT SUNITINIB MALATE 1 Oral 50 MG, CYCLIC (DAY 1-14 Q21 DAYS) Y 753CA 21938 50 MG CAPSULE, HARD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
114319193 11431919 1 Renal cell carcinoma

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
114319193 11431919 Diarrhoea
114319193 11431919 Emotional disorder
114319193 11431919 Fatigue
114319193 11431919 Feeling abnormal
114319193 11431919 Gastric disorder
114319193 11431919 Lethargy

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
114319193 11431919 1 20150817 0
114319193 11431919 2 20160617 0