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
124473903 12447390 3 F 20160621 20160608 20160705 EXP US-PFIZER INC-2016285550 PFIZER 60.00 YR M Y 0.00000 20160705 MD 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
124473903 12447390 1 PS SUTENT SUNITINIB MALATE 1 Oral 50 MG, CYCLIC (TAKE 1 CAPSULE BY MOUTH DAILY FOR 4 WEEKS THEN 2 WEEKS OFF) U 21938 50 MG CAPSULE, HARD
124473903 12447390 2 SS SUTENT SUNITINIB MALATE 1 50 MG, CYCLIC (28 DAYS ON/14 DAYS OFF) U 21938 50 MG CAPSULE, HARD
124473903 12447390 3 C COUMADIN WARFARIN SODIUM 1 UNK 0
124473903 12447390 4 C METOPROLOL. METOPROLOL 1 UNK 0
124473903 12447390 5 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 UNK 0
124473903 12447390 6 C LISINOPRIL. LISINOPRIL 1 UNK 0
124473903 12447390 7 C FLOMAX TAMSULOSIN HYDROCHLORIDE 1 UNK 0
124473903 12447390 8 C DOCUSATE DOCUSATE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124473903 12447390 1 Renal cell carcinoma

Outcome of event

Event ID CASEID OUTC COD
124473903 12447390 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124473903 12447390 Haemorrhagic cyst
124473903 12447390 Mobility decreased
124473903 12447390 Pain
124473903 12447390 Pain in extremity
124473903 12447390 Penile pain
124473903 12447390 Proctalgia
124473903 12447390 Testicular pain

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
124473903 12447390 1 20160429 0
124473903 12447390 2 20160506 0