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
127888191 12788819 1 I 20151127 20160928 20160928 EXP CA-PFIZER INC-2015421215 PFIZER 0.00 Y 0.00000 20160928 MD CA CA

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
127888191 12788819 1 PS SUNITINIB MALATE. SUNITINIB MALATE 1 25 MG, CYCLIC (4/2 SCHEDULE) Y 21938 25 MG
127888191 12788819 2 SS SUNITINIB MALATE. SUNITINIB MALATE 1 25 MG, CYCLIC (2 WEEKS ON/ 7-10 DAYS OFF) Y 21938 25 MG
127888191 12788819 3 SS SUNITINIB MALATE. SUNITINIB MALATE 1 25 MG, CYCLIC (10-14 DAYS ON/ 7-10 DAYS OFF) Y 21938 25 MG
127888191 12788819 4 C THYROXINE LEVOTHYROXINE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127888191 12788819 1 Metastatic renal cell carcinoma
127888191 12788819 4 Hormone replacement therapy

Outcome of event

Event ID CASEID OUTC COD
127888191 12788819 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127888191 12788819 Bone marrow failure
127888191 12788819 Diarrhoea
127888191 12788819 Hypothyroidism
127888191 12788819 Palmar-plantar erythrodysaesthesia syndrome
127888191 12788819 Stomatitis

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
127888191 12788819 1 2010 0
127888191 12788819 2 2010 201301 0
127888191 12788819 3 201310 0