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
122840268 12284026 8 F 201512 20160713 20160419 20160719 EXP US-BIOGEN-2016BI00221206 BIOGEN 36.54 YR F Y 0.00000 20160719 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
122840268 12284026 1 PS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) 125104 300 MG UNKNOWN
122840268 12284026 2 SS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) 125104 300 MG UNKNOWN
122840268 12284026 3 SS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) 125104 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122840268 12284026 1 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
122840268 12284026 Drug ineffective
122840268 12284026 Headache
122840268 12284026 Multiple sclerosis relapse
122840268 12284026 Optic neuritis

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
122840268 12284026 1 20090403 20130328 0
122840268 12284026 2 20140115 20160330 0
122840268 12284026 3 2009 20160331 0