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
124567693 12456769 3 F 2016 20160630 20160610 20160711 EXP US-BAYER-2016-109688 BAYER 55.00 YR A F Y 0.00000 20160711 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
124567693 12456769 1 PS NEXAVAR SORAFENIB 1 Oral 200 MG, BID 21923 200 MG FILM-COATED TABLET BID
124567693 12456769 2 SS NEXAVAR SORAFENIB 1 Oral 200 MG, QD 21923 200 MG FILM-COATED TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124567693 12456769 1 Hepatocellular carcinoma
124567693 12456769 2 Hepatocellular carcinoma

Outcome of event

Event ID CASEID OUTC COD
124567693 12456769 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124567693 12456769 Activities of daily living impaired
124567693 12456769 Asthenia
124567693 12456769 Bedridden
124567693 12456769 Decreased appetite
124567693 12456769 Diarrhoea
124567693 12456769 Gait disturbance
124567693 12456769 Groin pain
124567693 12456769 Impaired self-care
124567693 12456769 Pain in extremity
124567693 12456769 Tremor
124567693 12456769 Weight decreased
124567693 12456769 Wheelchair user

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
124567693 12456769 1 20160525 20160615 0
124567693 12456769 2 20160616 0