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
122065368 12206536 8 F 2016 20160906 20160324 20160915 PER US-PFIZER INC-2016149440 PFIZER 56.00 YR F Y 73.00000 KG 20160915 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
122065368 12206536 1 PS SUTENT SUNITINIB MALATE 1 50 MG, CYCLIC (28 DAYS ON/14 DAYS OFF) U 21938 50 MG CAPSULE, HARD
122065368 12206536 2 C BABY ASPIRIN ASPIRIN 1 UNK 0
122065368 12206536 3 C CALCIUM CALCIUM 1 UNK 0
122065368 12206536 4 C FERROUS SULFATE. FERROUS SULFATE 1 UNK 0
122065368 12206536 5 C TYLENOL ACETAMINOPHEN 1 UNK 0
122065368 12206536 6 C STOOL SOFTENER DOCUSATE CALCIUM 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122065368 12206536 1 Metastatic renal cell carcinoma

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
122065368 12206536 Abdominal pain
122065368 12206536 Acne
122065368 12206536 Diarrhoea
122065368 12206536 Dysgeusia
122065368 12206536 Dyspepsia
122065368 12206536 Eye swelling
122065368 12206536 Fatigue
122065368 12206536 Feeling abnormal
122065368 12206536 Flatulence
122065368 12206536 Hypotonia
122065368 12206536 Lacrimation increased
122065368 12206536 Oral pain
122065368 12206536 Skin disorder
122065368 12206536 Sleep disorder
122065368 12206536 Stomatitis
122065368 12206536 Swelling face
122065368 12206536 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
122065368 12206536 1 20160223 0