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
127299041 12729904 1 I 201608 20160818 20160909 20160909 EXP MX-BAYER-2016-163499 BAYER 64.00 YR A F Y 64.00000 KG 20160909 CN MX MX

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
127299041 12729904 1 PS NEXAVAR SORAFENIB 1 800 MG, QD 21923 800 MG FILM-COATED TABLET QD
127299041 12729904 2 C METOPROLOL. METOPROLOL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127299041 12729904 1 Hepatocellular carcinoma

Outcome of event

Event ID CASEID OUTC COD
127299041 12729904 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127299041 12729904 Abdominal pain upper
127299041 12729904 Asthenopia
127299041 12729904 Blood pressure increased
127299041 12729904 Burning sensation
127299041 12729904 Depressed mood
127299041 12729904 Erythema
127299041 12729904 Feeling hot
127299041 12729904 Gastrointestinal pain
127299041 12729904 Headache
127299041 12729904 Hunger
127299041 12729904 Hypersensitivity
127299041 12729904 Mass
127299041 12729904 Mouth swelling
127299041 12729904 Palpitations
127299041 12729904 Pruritus
127299041 12729904 Somnolence
127299041 12729904 Suffocation feeling
127299041 12729904 Swelling
127299041 12729904 Swelling face

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
127299041 12729904 1 20160815 0