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
127299651 12729965 1 I 201608 20160830 20160909 20160909 EXP MX-BAYER-2016-170936 BAYER 0.00 F Y 0.00000 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
127299651 12729965 1 PS NEXAVAR SORAFENIB 1 UNK 21923 FILM-COATED TABLET

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127299651 12729965 OT
127299651 12729965 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127299651 12729965 Anal ulcer
127299651 12729965 Anorectal discomfort
127299651 12729965 Blood pressure increased
127299651 12729965 Hypersensitivity
127299651 12729965 Mouth ulceration
127299651 12729965 Oral pain
127299651 12729965 Pain in extremity
127299651 12729965 Palmar-plantar erythrodysaesthesia syndrome
127299651 12729965 Proctalgia
127299651 12729965 Pyrexia
127299651 12729965 Stomatitis
127299651 12729965 Tonsillitis
127299651 12729965 Urticaria
127299651 12729965 Vulvovaginal discomfort
127299651 12729965 Vulvovaginal pain

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
127299651 12729965 1 20160818 0