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
124566323 12456632 3 F 201605 20160704 20160610 20160705 EXP MX-BAYER-2016-107791 BAYER 33.00 YR A F Y 50.00000 KG 20160705 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
124566323 12456632 1 PS NEXAVAR SORAFENIB 1 Oral 800 MG, QD 21923 800 MG FILM-COATED TABLET QD
124566323 12456632 2 C SIROLIMUS. SIROLIMUS 1 0
124566323 12456632 3 C PREDNISONE. PREDNISONE 1 0
124566323 12456632 4 C BUTILHIOSCINA 2 0
124566323 12456632 5 C AMITRIPTYLINE AMITRIPTYLINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124566323 12456632 1 Hepatocellular carcinoma

Outcome of event

Event ID CASEID OUTC COD
124566323 12456632 OT
124566323 12456632 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124566323 12456632 Cough
124566323 12456632 Depression
124566323 12456632 Diarrhoea
124566323 12456632 Fatigue
124566323 12456632 Feeling abnormal
124566323 12456632 Gait disturbance
124566323 12456632 Hepatitis
124566323 12456632 Hypophagia
124566323 12456632 Muscular weakness
124566323 12456632 Nausea
124566323 12456632 Neuralgia
124566323 12456632 Pain
124566323 12456632 Pain of skin
124566323 12456632 Pneumonia
124566323 12456632 Vomiting

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
124566323 12456632 1 20160527 0