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
125792157 12579215 7 F 2016 20160818 20160721 20160822 EXP MX-BAYER-2016-137357 BAYER 67.00 YR E M Y 68.00000 KG 20160822 CN MX MX

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
125792157 12579215 1 PS NEXAVAR SORAFENIB 1 800 MG, QD 44800 MG 21923 800 MG FILM-COATED TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125792157 12579215 1 Hepatocellular carcinoma

Outcome of event

Event ID CASEID OUTC COD
125792157 12579215 OT
125792157 12579215 DE
125792157 12579215 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125792157 12579215 Ascites
125792157 12579215 Asthenia
125792157 12579215 Constipation
125792157 12579215 Death
125792157 12579215 Decreased appetite
125792157 12579215 Depressed mood
125792157 12579215 Diarrhoea
125792157 12579215 Dyspnoea
125792157 12579215 Fatigue
125792157 12579215 Gait disturbance
125792157 12579215 Gastrointestinal disorder
125792157 12579215 Mobility decreased
125792157 12579215 Muscle fatigue
125792157 12579215 Nausea
125792157 12579215 Oral candidiasis
125792157 12579215 Pain in extremity
125792157 12579215 Palmar-plantar erythrodysaesthesia syndrome
125792157 12579215 Parosmia
125792157 12579215 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
125792157 12579215 1 20160620 20160814 0