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
111433956 11143395 6 F 20150422 20160801 20150528 20160812 EXP US-AMGEN-USACT2015041811 AMGEN 41.00 YR A F Y 56.80000 KG 20160812 MD 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
111433956 11143395 1 PS panitumumab PANITUMUMAB 1 Intravenous (not otherwise specified) 6 MG/KG, UNK 125147 6 MG/KG SOLUTION FOR INJECTION
111433956 11143395 2 SS MEK 162 BINIMETINIB 1 Oral 45 MG, BID 3870 MG 0 45 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
111433956 11143395 1 Colorectal cancer metastatic
111433956 11143395 2 Colorectal cancer metastatic

Outcome of event

Event ID CASEID OUTC COD
111433956 11143395 DE
111433956 11143395 LT
111433956 11143395 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
111433956 11143395 Anaemia
111433956 11143395 Hypoxia
111433956 11143395 Platelet count decreased
111433956 11143395 Sinus tachycardia

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
111433956 11143395 1 20150310 20150421 0
111433956 11143395 2 20150310 20150421 0