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
123320353 12332035 3 F 20160718 20160504 20160729 PER US-PFIZER INC-2016239135 PFIZER 63.00 YR F Y 58.20000 KG 20160729 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
123320353 12332035 1 PS SUTENT SUNITINIB MALATE 1 Oral 50 MG, DAILY Y 21938 50 MG CAPSULE, HARD
123320353 12332035 2 SS SUTENT SUNITINIB MALATE 1 Oral 25 MG, CYCLIC (DAILY FOR 21 OUT OF 28 DAYS) Y 21938 25 MG CAPSULE, HARD
123320353 12332035 3 C TRAMADIN 2 UNK 0
123320353 12332035 4 C WARFARIN WARFARIN 1 UNK 0
123320353 12332035 5 C ZOFRAN ONDANSETRON HYDROCHLORIDE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123320353 12332035 1 Gastrointestinal stromal tumour

Outcome of event

Event ID CASEID OUTC COD
123320353 12332035 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123320353 12332035 Ageusia
123320353 12332035 Decreased appetite
123320353 12332035 Diarrhoea
123320353 12332035 Fatigue
123320353 12332035 Feeling abnormal
123320353 12332035 Headache
123320353 12332035 Leukopenia
123320353 12332035 Nausea
123320353 12332035 Tongue discomfort

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
123320353 12332035 1 201601 0
123320353 12332035 2 20160315 0