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
112876067 11287606 7 F 20151119 20160912 20150721 20160913 PER US-PFIZER INC-2015238042 PFIZER 77.00 YR M Y 79.38000 KG 20160913 MD 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
112876067 11287606 1 PS SUTENT SUNITINIB MALATE 1 50 MG, CYCLIC (FOR 4 WEEKS THEN OFF FOR 2 WEEKS) Y X731C 21938 50 MG CAPSULE, HARD
112876067 11287606 2 SS SUTENT SUNITINIB MALATE 1 37.5 MG, UNK Y 21938 37.5 MG CAPSULE, HARD
112876067 11287606 3 SS SUTENT SUNITINIB MALATE 1 Oral 37.5 MG, 1X/DAY Y 21938 37.5 MG CAPSULE, HARD QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
112876067 11287606 1 Renal cancer stage IV

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
112876067 11287606 Activities of daily living impaired
112876067 11287606 Anxiety
112876067 11287606 Bladder disorder
112876067 11287606 Blood pressure increased
112876067 11287606 Disease progression
112876067 11287606 Fatigue
112876067 11287606 Gait disturbance
112876067 11287606 Hypokinesia
112876067 11287606 Movement disorder
112876067 11287606 Mucosal inflammation
112876067 11287606 Oropharyngeal pain
112876067 11287606 Renal cancer stage IV
112876067 11287606 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
112876067 11287606 1 20150430 0
112876067 11287606 2 20150901 0
112876067 11287606 3 201506 20160822 0