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
124954682 12495468 2 F 20160628 20160624 20160707 EXP ZA-BAYER-2016-123399 BAYER 35.00 YR A M Y 0.00000 20160707 OT ZA ZA

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
124954682 12495468 1 PS NEXAVAR SORAFENIB 1 Oral 400 MG, UNK 21923 400 MG FILM-COATED TABLET
124954682 12495468 2 SS NEXAVAR SORAFENIB 1 Oral 400 MG, UNK 21923 400 MG FILM-COATED TABLET
124954682 12495468 3 SS NEXAVAR SORAFENIB 1 Oral 400 MG, UNK 21923 400 MG FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124954682 12495468 1 Hepatocellular carcinoma
124954682 12495468 2 Hepatocellular carcinoma
124954682 12495468 3 Hepatocellular carcinoma

Outcome of event

Event ID CASEID OUTC COD
124954682 12495468 HO
124954682 12495468 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
124954682 12495468 Dyspnoea
124954682 12495468 Haemoglobin decreased
124954682 12495468 Hepatocellular carcinoma

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
124954682 12495468 1 20160309 2016 0
124954682 12495468 2 20160411 2016 0
124954682 12495468 3 20160509 0