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
124434484 12443448 4 F 201604 20160701 20160607 20160713 EXP US-BIOGEN-2016BI00244236 BIOGEN 59.04 YR M Y 0.00000 20160713 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
124434484 12443448 1 PS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) Y 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION
124434484 12443448 2 SS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) Y 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124434484 12443448 1 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124434484 12443448 Depression
124434484 12443448 Gastroenteritis
124434484 12443448 Neurological decompensation
124434484 12443448 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
124434484 12443448 1 20111031 20130422 0
124434484 12443448 2 20140421 20160427 0