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
126251401 12625140 1 I 201607 20160728 20160805 20160805 EXP US-BAYER-2016-148399 BAYER 59.00 YR A M Y 0.00000 20160805 OT 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
126251401 12625140 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
126251401 12625140 1 Acute myeloid leukaemia

Outcome of event

Event ID CASEID OUTC COD
126251401 12625140 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126251401 12625140 Decreased appetite
126251401 12625140 Diarrhoea
126251401 12625140 Dry skin
126251401 12625140 Fatigue
126251401 12625140 Haemoglobin decreased
126251401 12625140 Laboratory test abnormal
126251401 12625140 Off label use
126251401 12625140 Platelet count decreased
126251401 12625140 Pyrexia
126251401 12625140 White blood cell count 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
126251401 12625140 1 20160715 0