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
124246354 12424635 4 F 201605 20160902 20160601 20160902 EXP IE-BAYER-2016-098875 BAYER 68.00 YR E M Y 0.00000 20160902 CN IE IE

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
124246354 12424635 1 PS NEXAVAR SORAFENIB 1 Oral 200 MG, BID G88133 21923 200 MG FILM-COATED TABLET BID
124246354 12424635 2 SS NEXAVAR SORAFENIB 1 21923 FILM-COATED TABLET
124246354 12424635 3 C INSULIN INSULIN NOS 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124246354 12424635 1 Hepatocellular carcinoma
124246354 12424635 2 Hepatic cancer
124246354 12424635 3 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
124246354 12424635 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124246354 12424635 Abdominal pain
124246354 12424635 Aspiration
124246354 12424635 Blood glucose decreased
124246354 12424635 Blood pressure increased
124246354 12424635 Decreased appetite
124246354 12424635 Disorientation
124246354 12424635 Dizziness
124246354 12424635 Dysarthria
124246354 12424635 Dysphagia
124246354 12424635 Dyspnoea
124246354 12424635 Flatulence
124246354 12424635 Gastrooesophageal reflux disease
124246354 12424635 Infection
124246354 12424635 Malaise
124246354 12424635 Nausea
124246354 12424635 Oesophageal food impaction

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
124246354 12424635 1 20160511 20160521 0