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
125561342 12556134 2 F 201607 20160708 20160714 20160715 EXP US-BAYER-2016-133239 BAYER 77.00 YR E F Y 0.00000 20160715 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
125561342 12556134 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
125561342 12556134 1 Hepatocellular carcinoma

Outcome of event

Event ID CASEID OUTC COD
125561342 12556134 OT
125561342 12556134 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125561342 12556134 Abdominal pain
125561342 12556134 Asthenia
125561342 12556134 Blood pressure increased
125561342 12556134 Decreased appetite
125561342 12556134 Dehydration
125561342 12556134 Diarrhoea
125561342 12556134 Fatigue
125561342 12556134 Incontinence
125561342 12556134 Lethargy
125561342 12556134 Slow response to stimuli

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
125561342 12556134 1 20160701 201607 0