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
127375001 12737500 1 I 2016 20160811 20160913 20160913 EXP BR-BAYER-2016-156854 BAYER 0.00 E F Y 0.00000 20160913 CN BR BR

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
127375001 12737500 1 PS NEXAVAR SORAFENIB 1 Oral 4 DF, QD Y 21923 4 DF FILM-COATED TABLET QD
127375001 12737500 2 SS NEXAVAR SORAFENIB 1 Oral 2 DF, QD Y 21923 2 DF FILM-COATED TABLET QD

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127375001 12737500 OT
127375001 12737500 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127375001 12737500 Adverse event
127375001 12737500 Chapped lips
127375001 12737500 Decreased appetite
127375001 12737500 Delirium
127375001 12737500 Gait disturbance
127375001 12737500 Lip exfoliation
127375001 12737500 Lip haemorrhage
127375001 12737500 Pyrexia
127375001 12737500 Skin exfoliation
127375001 12737500 Skin hypertrophy
127375001 12737500 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
127375001 12737500 1 2016 2016 0
127375001 12737500 2 2016 2016 0