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
123602705 12360270 5 F 20160701 20160512 20160713 PER US-PFIZER INC-2016246147 PFIZER 71.00 YR M Y 68.00000 KG 20160713 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
123602705 12360270 1 PS SUTENT SUNITINIB MALATE 1 50 MG, CYCLIC (28 DAYS ON/14 DAYS OFF) Y 21938 50 MG CAPSULE, HARD
123602705 12360270 2 C AMLODIPINE AMLODIPINE BESYLATE 1 UNK 0
123602705 12360270 3 C GLIPIZIDE. GLIPIZIDE 1 UNK 0
123602705 12360270 4 C LEXAPRO ESCITALOPRAM OXALATE 1 UNK 0
123602705 12360270 5 C METOPROLOL. METOPROLOL 1 UNK 0
123602705 12360270 6 C NORCO ACETAMINOPHENHYDROCODONE BITARTRATE 1 UNK 0
123602705 12360270 7 C LIPITOR ATORVASTATIN CALCIUM 1 UNK 0
123602705 12360270 8 C VITAMIN D CHOLECALCIFEROL 1 UNK 0
123602705 12360270 9 C NYSTATIN. NYSTATIN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123602705 12360270 1 Renal cancer stage IV

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123602705 12360270 Arthralgia
123602705 12360270 Asthenia
123602705 12360270 Disease progression
123602705 12360270 Fatigue
123602705 12360270 Gait disturbance
123602705 12360270 Hypersomnia
123602705 12360270 Hypophagia
123602705 12360270 Malaise
123602705 12360270 Renal cancer stage IV
123602705 12360270 Stomatitis
123602705 12360270 Weight decreased

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
123602705 12360270 1 20160426 20160523 0