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
127634381 12763438 1 I 201605 20160519 20160920 20160920 EXP CA-BAYER-2016-098407 BAYER 64.00 YR A F Y 0.00000 20160920 OT CA CA

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
127634381 12763438 1 PS NEXAVAR SORAFENIB 1 Oral UNK 21923 FILM-COATED TABLET
127634381 12763438 2 SS NEXAVAR SORAFENIB 1 Oral 400 MG DAILY 21923 400 MG FILM-COATED TABLET
127634381 12763438 3 C NADOLOL. NADOLOL 1 0
127634381 12763438 4 C AMLODIPINE AMLODIPINE BESYLATE 1 0
127634381 12763438 5 C CALCIUM CALCIUM 1 0
127634381 12763438 6 C VITAMIN D CHOLECALCIFEROL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127634381 12763438 1 Hepatocellular carcinoma
127634381 12763438 2 Hepatocellular carcinoma

Outcome of event

Event ID CASEID OUTC COD
127634381 12763438 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127634381 12763438 Alopecia
127634381 12763438 Ammonia abnormal
127634381 12763438 Ammonia increased
127634381 12763438 Confusional state
127634381 12763438 Contrast media allergy
127634381 12763438 Fatigue
127634381 12763438 Hypertension
127634381 12763438 Syncope
127634381 12763438 Toxicity to various agents
127634381 12763438 Underdose

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
127634381 12763438 1 20160516 0
127634381 12763438 2 201605 0