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
127580051 12758005 1 I 201607 20160803 20160919 20160919 EXP US-BAYER-2016-152217 BAYER 65.61 YR E M Y 0.00000 20160919 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
127580051 12758005 1 PS NEXAVAR SORAFENIB 1 Oral 200 MG, BID Y 21923 200 MG FILM-COATED TABLET BID
127580051 12758005 2 SS NEXAVAR SORAFENIB 1 Oral 400 MG, BID Y 21923 400 MG FILM-COATED TABLET BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127580051 12758005 1 Hepatocellular carcinoma
127580051 12758005 2 Hepatocellular carcinoma

Outcome of event

Event ID CASEID OUTC COD
127580051 12758005 OT
127580051 12758005 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127580051 12758005 Abdominal pain
127580051 12758005 Blister
127580051 12758005 Blood pressure fluctuation
127580051 12758005 Blood pressure increased
127580051 12758005 Chest pain
127580051 12758005 Constipation
127580051 12758005 Diarrhoea
127580051 12758005 Oedema peripheral
127580051 12758005 Orthostatic hypertension
127580051 12758005 Peripheral swelling
127580051 12758005 Pruritus
127580051 12758005 Pyrexia

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
127580051 12758005 1 20160729 2016 0
127580051 12758005 2 20160805 2016 0