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
119101197 11910119 7 F 2015 20160615 20160112 20160711 PER PR-PFIZER INC-2015349732 PFIZER 64.00 YR M Y 0.00000 20160711 CN PR PR

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
119101197 11910119 1 PS SUTENT SUNITINIB MALATE 1 Oral 50 MG, CYCLIC (DAILY X 4 WEEKS, THEN 2 WEEKS OFF) 21938 50 MG CAPSULE, HARD
119101197 11910119 2 SS SUTENT SUNITINIB MALATE 1 50 MG, CYCLIC (28 DAYS ON/14 DAYS OFF) 21938 50 MG CAPSULE, HARD
119101197 11910119 3 C AVAPRO IRBESARTAN 1 150 MG, UNK 0 150 MG
119101197 11910119 4 C OMEPRAZOLE. OMEPRAZOLE 1 20 MG, UNK 0 20 MG
119101197 11910119 5 C PREPARATION H NOS COCOA BUTTERPETROLATUMPHENYLEPHRINE HYDROCHLORIDEPHENYLEPHRINE HYDROCHLORIDE OR MINERAL OIL 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119101197 11910119 1 Renal cancer stage IV
119101197 11910119 2 Renal cancer

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
119101197 11910119 Abdominal discomfort
119101197 11910119 Anorectal discomfort
119101197 11910119 Asthenia
119101197 11910119 Back pain
119101197 11910119 Decreased appetite
119101197 11910119 Diarrhoea
119101197 11910119 Dry skin
119101197 11910119 Dysgeusia
119101197 11910119 Gingival discomfort
119101197 11910119 Oral discomfort
119101197 11910119 Oral pain
119101197 11910119 Pain in extremity
119101197 11910119 Palmar-plantar erythrodysaesthesia syndrome
119101197 11910119 Skin disorder
119101197 11910119 Skin hypertrophy
119101197 11910119 Temperature intolerance
119101197 11910119 Throat irritation
119101197 11910119 Tongue discomfort
119101197 11910119 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
119101197 11910119 1 20151120 0
119101197 11910119 2 20151120 0