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
125284842 12528484 2 F 2016 20160715 20160705 20160722 EXP US-BAYER-2016-124037 BAYER 27.00 YR A M Y 0.00000 20160722 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
125284842 12528484 1 PS NEXAVAR SORAFENIB 1 Oral 400 MG, BID Y 21923 400 MG FILM-COATED TABLET BID
125284842 12528484 2 SS NEXAVAR SORAFENIB 1 Oral 200 MG, BID Y 21923 200 MG FILM-COATED TABLET BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125284842 12528484 1 Hepatocellular carcinoma
125284842 12528484 2 Hepatocellular carcinoma

Outcome of event

Event ID CASEID OUTC COD
125284842 12528484 HO
125284842 12528484 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125284842 12528484 Abdominal pain
125284842 12528484 Decreased appetite
125284842 12528484 Dyspnoea
125284842 12528484 Epistaxis
125284842 12528484 Heart rate increased
125284842 12528484 Pulmonary oedema
125284842 12528484 Pyrexia
125284842 12528484 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
125284842 12528484 1 20160616 20160624 0
125284842 12528484 2 20160707 0