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
120134036 12013403 6 F 201505 20160804 20160205 20160808 EXP US-BIOGEN-2015BI077950 BIOGEN 51.10 YR F Y 0.00000 20160808 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
120134036 12013403 1 PS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) INFUSED OVER 1 HOUR Y 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION
120134036 12013403 2 SS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) INFUSED OVER 1 HOUR Y 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120134036 12013403 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
120134036 12013403 HO
120134036 12013403 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
120134036 12013403 Breast cancer
120134036 12013403 Gait disturbance
120134036 12013403 Myelodysplastic syndrome

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
120134036 12013403 1 20130422 20160406 0
120134036 12013403 2 20130422 20150429 0