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
124679663 12467966 3 F 20120705 20160916 20160615 20160927 EXP JP-PFIZER INC-2016295796 PFIZER 81.00 YR M Y 54.70000 KG 20160927 PH JP JP

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
124679663 12467966 1 PS SUTENT SUNITINIB MALATE 1 Oral 50 MG, DAILY Y 21938 50 MG CAPSULE, HARD
124679663 12467966 2 SS SUTENT SUNITINIB MALATE 1 Oral 50 MG, DAILY Y 21938 50 MG CAPSULE, HARD
124679663 12467966 3 SS SUTENT SUNITINIB MALATE 1 Oral 25 MG, DAILY Y 21938 25 MG CAPSULE, HARD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124679663 12467966 1 Renal cell carcinoma

Outcome of event

Event ID CASEID OUTC COD
124679663 12467966 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124679663 12467966 Bone marrow failure
124679663 12467966 Liver disorder
124679663 12467966 Nausea
124679663 12467966 Palmar-plantar erythrodysaesthesia syndrome

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
124679663 12467966 1 20120607 0
124679663 12467966 2 20120830 0
124679663 12467966 3 20160813 0