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
123186924 12318692 4 F 201604 20160707 20160429 20160718 EXP US-BAYER-2016-077524 BAYER 57.00 YR A M Y 0.00000 20160718 MD 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
123186924 12318692 1 PS NEXAVAR SORAFENIB 1 Oral 200 MG, BID 21923 200 MG FILM-COATED TABLET BID
123186924 12318692 2 SS NEXAVAR SORAFENIB 1 Oral 200 MG, QD 21923 200 MG FILM-COATED TABLET QD
123186924 12318692 3 C DIPHENOXYLATE DIPHENOXYLATE 1 0
123186924 12318692 4 C LACTOFERMENT [LACTOBACILLUS NOS] 2 0
123186924 12318692 5 C OXYCODONE OXYCODONE 1 Oral 200 MG, QD 0 200 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123186924 12318692 1 Hepatocellular carcinoma
123186924 12318692 2 Hepatocellular carcinoma

Outcome of event

Event ID CASEID OUTC COD
123186924 12318692 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123186924 12318692 Abdominal discomfort
123186924 12318692 Abdominal distension
123186924 12318692 Abdominal pain
123186924 12318692 Abdominal rigidity
123186924 12318692 Breath sounds abnormal
123186924 12318692 Diarrhoea
123186924 12318692 Dizziness
123186924 12318692 Erectile dysfunction
123186924 12318692 Fatigue
123186924 12318692 Headache
123186924 12318692 Hypertension
123186924 12318692 Muscle spasms

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
123186924 12318692 1 20160317 201603 0
123186924 12318692 2 20160504 0
123186924 12318692 5 20160504 0