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
125218793 12521879 3 F 20160504 20160712 20160701 20160720 EXP MX-BAYER-2016-089630 BAYER 69.00 YR E F Y 55.50000 KG 20160720 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
125218793 12521879 1 PS NEXAVAR SORAFENIB 1 Oral UNK 21923 FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125218793 12521879 1 Hepatocellular carcinoma

Outcome of event

Event ID CASEID OUTC COD
125218793 12521879 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125218793 12521879 Alopecia
125218793 12521879 Depression
125218793 12521879 Fatigue
125218793 12521879 General physical health deterioration
125218793 12521879 Hepatocellular carcinoma
125218793 12521879 Influenza
125218793 12521879 Mass
125218793 12521879 Peripheral swelling
125218793 12521879 Sensitivity to weather change
125218793 12521879 Skin induration
125218793 12521879 Weight decreased

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
125218793 12521879 1 201512 0