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
103902877 10390287 7 F 201406 20160909 20140818 20160922 EXP US-PFIZER INC-2014224126 PFIZER 53.00 YR M Y 0.00000 20160922 CN 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
103902877 10390287 1 PS SUTENT SUNITINIB MALATE 1 Oral 50 MG, DAILY (10 DAYS ON; 7 DAYS OFF) Y 21938 50 MG CAPSULE, HARD
103902877 10390287 2 SS SUTENT SUNITINIB MALATE 1 UNK, 1 A DAY 4 WEEKS ON 2 WEEKS OFF Y 21938 CAPSULE, HARD
103902877 10390287 3 SS SUTENT SUNITINIB MALATE 1 UNK (2 WEEKS ON / 1 WEEK OFF) Y 21938 CAPSULE, HARD
103902877 10390287 4 SS SUTENT SUNITINIB MALATE 1 UNK (10DAYS ON / 7 DAYS OFF) Y 21938 CAPSULE, HARD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
103902877 10390287 1 Metastatic renal cell carcinoma

Outcome of event

Event ID CASEID OUTC COD
103902877 10390287 HO
103902877 10390287 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
103902877 10390287 Blister
103902877 10390287 Disease progression
103902877 10390287 Drug intolerance
103902877 10390287 Hair colour changes
103902877 10390287 Hyperkeratosis
103902877 10390287 Metastatic renal cell carcinoma
103902877 10390287 Pain in extremity
103902877 10390287 Pneumothorax
103902877 10390287 Skin exfoliation

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
103902877 10390287 1 20140228 20140924 0
103902877 10390287 3 201403 0