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
101449826 10144982 6 F 20140417 20160708 20140501 20160720 EXP FR-AMGEN-FRACT2014031353 AMGEN 42.00 YR A F Y 38.00000 KG 20160720 MD FR FR

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
101449826 10144982 1 PS panitumumab PANITUMUMAB 1 Intravenous (not otherwise specified) 6 MG/KG, Q2WK (CYCLIC EVERY 2 WEEKS) 125147 6 MG/KG SOLUTION FOR INJECTION QOW
101449826 10144982 2 SS DABRAFENIB DABRAFENIB 1 Oral 150 MG, BID Y 0 150 MG CAPSULE BID
101449826 10144982 3 SS DABRAFENIB DABRAFENIB 1 Oral 150 MG, UNK Y 0 150 MG CAPSULE
101449826 10144982 4 SS DABRAFENIB DABRAFENIB 1 Oral 200 MG, UNK Y 0 200 MG CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
101449826 10144982 1 Colorectal cancer
101449826 10144982 2 Colorectal cancer

Outcome of event

Event ID CASEID OUTC COD
101449826 10144982 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
101449826 10144982 Diarrhoea haemorrhagic
101449826 10144982 Pyrexia

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
101449826 10144982 1 20140407 0
101449826 10144982 2 20140407 20140419 0
101449826 10144982 3 20150420 20150420 0
101449826 10144982 4 20140424 0