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
123934392 12393439 2 F 201407 20160727 20160523 20160803 EXP GB-BAYER-2016-093418 BAYER 78.00 YR E M Y 0.00000 20160803 OT GB GB

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
123934392 12393439 1 PS NEXAVAR SORAFENIB 1 Oral 400 MG, BID Y 21923 400 MG FILM-COATED TABLET BID
123934392 12393439 2 SS NEXAVAR SORAFENIB 1 200 MG DAILY Y 21923 FILM-COATED TABLET
123934392 12393439 3 C TENOFOVIR TENOFOVIR 1 245 MG DAILY 0
123934392 12393439 4 C ATENOLOL. ATENOLOL 1 100MG DAILY 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123934392 12393439 1 Hepatocellular carcinoma
123934392 12393439 2 Hepatocellular carcinoma
123934392 12393439 3 Hepatitis B
123934392 12393439 4 Hypertension

Outcome of event

Event ID CASEID OUTC COD
123934392 12393439 OT
123934392 12393439 HO
123934392 12393439 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
123934392 12393439 Back pain Back pain
123934392 12393439 Fatigue
123934392 12393439 Hepatic failure
123934392 12393439 Hepatocellular carcinoma
123934392 12393439 Neoplasm malignant
123934392 12393439 Rash
123934392 12393439 Skin reaction
123934392 12393439 Spinal cord compression Spinal cord compression

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
123934392 12393439 1 201407 201410 0