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
127850581 12785058 1 I 20160519 20160512 20160927 20160927 EXP ID-BAYER-2016-092546 BAYER 61.00 YR A M Y 0.00000 20160927 OT ID ID

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
127850581 12785058 1 PS NEXAVAR SORAFENIB 1 Oral 2 X 200 MG Y 21923 FILM-COATED TABLET
127850581 12785058 2 SS NEXAVAR SORAFENIB 1 Oral 2X200 MG Y 21923 400 MG FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127850581 12785058 1 Hepatocellular carcinoma
127850581 12785058 2 Hepatocellular carcinoma

Outcome of event

Event ID CASEID OUTC COD
127850581 12785058 OT
127850581 12785058 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127850581 12785058 Blood electrolytes decreased
127850581 12785058 Diarrhoea
127850581 12785058 Dysphonia
127850581 12785058 Encephalopathy
127850581 12785058 Fall
127850581 12785058 Fatigue
127850581 12785058 Frequent bowel movements
127850581 12785058 Gait disturbance
127850581 12785058 Hypertension
127850581 12785058 Insomnia
127850581 12785058 Laryngitis
127850581 12785058 Malaise
127850581 12785058 Pain in extremity
127850581 12785058 Palmoplantar keratoderma
127850581 12785058 Platelet count decreased
127850581 12785058 Pruritus
127850581 12785058 Rash
127850581 12785058 Unevaluable event
127850581 12785058 Vomiting

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
127850581 12785058 1 20160413 201606 0
127850581 12785058 2 201606 0