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
118372597 11837259 7 F 20160705 20151215 20160714 PER US-PFIZER INC-2015422222 PFIZER 70.00 YR M Y 99.77000 KG 20160714 OT 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
118372597 11837259 1 PS SUTENT SUNITINIB MALATE 1 Oral 50 MG, CYCLIC (2 WEEKS ON, 1 WEEK OFF) U 090BA, 421BA 21938 50 MG CAPSULE, HARD
118372597 11837259 2 SS SUTENT SUNITINIB MALATE 1 Oral 37.5 MG, 1X/DAY U X731C 21938 37.5 MG CAPSULE, HARD QD
118372597 11837259 3 SS SUTENT SUNITINIB MALATE 1 Oral 37.5 MG, CYCLIC (DAYS 1-14 EVERY 21 DAYS) U X731B 21938 37.5 MG CAPSULE, HARD
118372597 11837259 4 SS SUTENT SUNITINIB MALATE 1 Oral 37.5 MG, CYCLIC (DAYS 1-14 EVERY 21 DAYS) U 258CA 21938 37.5 MG CAPSULE, HARD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118372597 11837259 1 Metastatic renal cell carcinoma

Outcome of event

Event ID CASEID OUTC COD
118372597 11837259 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
118372597 11837259 Constipation
118372597 11837259 Cough
118372597 11837259 Dry skin
118372597 11837259 Dysgeusia
118372597 11837259 Fatigue
118372597 11837259 Hyperthyroidism
118372597 11837259 Nasopharyngitis
118372597 11837259 Pain in extremity
118372597 11837259 Pruritus

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
118372597 11837259 1 20151023 0
118372597 11837259 2 20160209 0
118372597 11837259 4 20151023 0