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
126027401 12602740 1 I 2015 20150820 20160728 20160728 EXP IN-PFIZER INC-2015281178 PFIZER 72.00 YR M Y 0.00000 20160728 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
126027401 12602740 1 PS SUTENT SUNITINIB MALATE 1 Oral 25 MG, 1X/DAY Y 21938 25 MG CAPSULE, HARD QD
126027401 12602740 2 SS SUTENT SUNITINIB MALATE 1 UNK Y 21938 CAPSULE, HARD
126027401 12602740 3 SS SUTENT SUNITINIB MALATE 1 Oral 25 UNK, UNK Y 21938 25 MG CAPSULE, HARD QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126027401 12602740 1 Metastatic renal cell carcinoma

Outcome of event

Event ID CASEID OUTC COD
126027401 12602740 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126027401 12602740 Abdominal pain
126027401 12602740 Anaemia
126027401 12602740 Asthenia
126027401 12602740 Blister
126027401 12602740 Burning sensation
126027401 12602740 Disease progression
126027401 12602740 Dizziness
126027401 12602740 Dry skin
126027401 12602740 Frequent bowel movements
126027401 12602740 Hypoalbuminaemia
126027401 12602740 Lacrimation increased
126027401 12602740 Metastatic renal cell carcinoma
126027401 12602740 Oedema
126027401 12602740 Skin discolouration
126027401 12602740 Skin exfoliation
126027401 12602740 Vertigo

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
126027401 12602740 1 20150405 20150903 0
126027401 12602740 2 20150914 20151113 0
126027401 12602740 3 20160606 0