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
126781682 12678168 2 F 201607 20160829 20160823 20160906 EXP US-BAYER-2016-141120 BAYER 54.00 YR A F Y 0.00000 20160906 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
126781682 12678168 1 PS NEXAVAR SORAFENIB 1 Oral 400 MG, BID 28800 MG BXH9XU1 21923 400 MG FILM-COATED TABLET BID
126781682 12678168 2 SS NEXAVAR SORAFENIB 1 Oral 200 MG, BID 28800 MG 21923 200 MG FILM-COATED TABLET BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126781682 12678168 1 Hepatocellular carcinoma
126781682 12678168 2 Hepatocellular carcinoma

Outcome of event

Event ID CASEID OUTC COD
126781682 12678168 HO
126781682 12678168 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126781682 12678168 Abdominal pain
126781682 12678168 Asthenia
126781682 12678168 Decreased activity
126781682 12678168 Decreased appetite
126781682 12678168 Fatigue
126781682 12678168 Gait disturbance
126781682 12678168 Nausea
126781682 12678168 Rehabilitation therapy

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
126781682 12678168 1 20160627 20160726 0
126781682 12678168 2 20160728 20160808 0