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
123224316 12322431 6 F 2016 20160719 20160502 20160729 EXP US-BAYER-2016-078510 BAYER 55.00 YR A M Y 0.00000 20160729 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
123224316 12322431 1 PS NEXAVAR SORAFENIB 1 Oral 400 MG, BID 21923 400 MG FILM-COATED TABLET BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123224316 12322431 1 Hepatocellular carcinoma

Outcome of event

Event ID CASEID OUTC COD
123224316 12322431 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123224316 12322431 Balance disorder
123224316 12322431 Blister
123224316 12322431 Blood bilirubin increased
123224316 12322431 Blood pressure increased
123224316 12322431 Constipation
123224316 12322431 Decreased appetite
123224316 12322431 Diarrhoea
123224316 12322431 Fatigue
123224316 12322431 Headache
123224316 12322431 Heart rate abnormal
123224316 12322431 Heart rate decreased
123224316 12322431 Nasal congestion
123224316 12322431 Nausea
123224316 12322431 Pain in extremity
123224316 12322431 Pain of skin
123224316 12322431 Rash papular
123224316 12322431 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
123224316 12322431 1 20160413 0