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
127999681 12799968 1 I 20081231 20160921 20160930 20160930 EXP SI-BAYER-2016-183610 BAYER 55.00 YR A M Y 0.00000 20160930 MD SI SI

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
127999681 12799968 1 PS NEXAVAR SORAFENIB 1 UNK D 21923 FILM-COATED TABLET
127999681 12799968 2 C TRANEXAMIC ACID. TRANEXAMIC ACID 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127999681 12799968 1 Hepatocellular carcinoma

Outcome of event

Event ID CASEID OUTC COD
127999681 12799968 HO
127999681 12799968 DE
127999681 12799968 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127999681 12799968 Ascites
127999681 12799968 Asthenia
127999681 12799968 Death
127999681 12799968 Diarrhoea
127999681 12799968 Gastrointestinal haemorrhage
127999681 12799968 Hepatic cirrhosis
127999681 12799968 Hepatic encephalopathy
127999681 12799968 Malaise
127999681 12799968 Oedema
127999681 12799968 Peritonitis bacterial
127999681 12799968 Sepsis
127999681 12799968 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
127999681 12799968 1 200810 0