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
122727933 12272793 3 F 201511 20160715 20160415 20160720 EXP US-BIOGEN-2015BI150708 BIOGEN 39.42 YR F Y 0.00000 20160720 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
122727933 12272793 1 PS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION
122727933 12272793 2 SS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION
122727933 12272793 3 SS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION
122727933 12272793 4 C BACLOFEN. BACLOFEN 1 Oral 0 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122727933 12272793 1 Multiple sclerosis
122727933 12272793 4 Muscle spasms

Outcome of event

Event ID CASEID OUTC COD
122727933 12272793 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
122727933 12272793 Complication associated with device
122727933 12272793 Pain
122727933 12272793 Urinary tract infection

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
122727933 12272793 1 20030101 0
122727933 12272793 2 20080611 20100317 0
122727933 12272793 3 20120911 0