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
123557502 12355750 2 F 20160112 20160704 20160511 20160712 EXP MX-BAYER-2016-027072 BAYER 39.00 YR A F Y 0.00000 20160712 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
123557502 12355750 1 PS NEXAVAR SORAFENIB 1 Oral 400 MG, BID 21923 400 MG FILM-COATED TABLET BID
123557502 12355750 2 C LOSARTAN. LOSARTAN 1 UNK 0 BID
123557502 12355750 3 C AMLODIPINE AMLODIPINE BESYLATE 1 UNK 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123557502 12355750 1 Hepatocellular carcinoma

Outcome of event

Event ID CASEID OUTC COD
123557502 12355750 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123557502 12355750 Alopecia
123557502 12355750 Blood pressure inadequately controlled
123557502 12355750 Diarrhoea
123557502 12355750 Dry skin
123557502 12355750 Erythema
123557502 12355750 Fatigue
123557502 12355750 Gingival bleeding
123557502 12355750 Hyperaesthesia
123557502 12355750 Hyperkeratosis
123557502 12355750 Hypoaesthesia
123557502 12355750 Limb discomfort
123557502 12355750 Mucosal ulceration
123557502 12355750 Paraesthesia
123557502 12355750 Tongue discomfort
123557502 12355750 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
123557502 12355750 1 20160112 0