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
115231835 11523183 5 F 20150821 20160913 20150918 20160923 EXP US-BAYER-2015-419243 BAYER 14.00 YR T M Y 0.00000 20160923 CN US US

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
115231835 11523183 1 PS NEXAVAR SORAFENIB 1 Oral 350 MG, QD 7350 MG 21923 350 MG FILM-COATED TABLET QD
115231835 11523183 2 SS NEXAVAR SORAFENIB 1 Oral 200 MG, BID 7350 MG 21923 200 MG FILM-COATED TABLET BID
115231835 11523183 3 C CYTARABINE. CYTARABINE 1 0
115231835 11523183 4 C DAUNORUBICIN DAUNORUBICIN 1 0
115231835 11523183 5 C ETOPOSIDE. ETOPOSIDE 1 0
115231835 11523183 6 C ACYCLOVIR [ACICLOVIR] ACYCLOVIR 1 0
115231835 11523183 7 C CASPOFUNGIN CASPOFUNGIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
115231835 11523183 1 Acute myeloid leukaemia
115231835 11523183 2 Acute myeloid leukaemia

Outcome of event

Event ID CASEID OUTC COD
115231835 11523183 HO
115231835 11523183 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
115231835 11523183 Bone marrow transplant
115231835 11523183 Dysaesthesia
115231835 11523183 Hospitalisation
115231835 11523183 Hypertension
115231835 11523183 Hypoaesthesia
115231835 11523183 Infection
115231835 11523183 Malaise
115231835 11523183 Off label use
115231835 11523183 Pain in extremity
115231835 11523183 Pancytopenia

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
115231835 11523183 1 20150801 20150829 0