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
122041775 12204177 5 F 201603 20160715 20160323 20160721 EXP US-BIOGEN-2016BI00208890 BIOGEN 39.75 YR F Y 0.00000 20160721 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
122041775 12204177 1 PS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION
122041775 12204177 2 SS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION
122041775 12204177 3 SS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122041775 12204177 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
122041775 12204177 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
122041775 12204177 Decubitus ulcer
122041775 12204177 Memory impairment
122041775 12204177 Mobility decreased

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
122041775 12204177 1 20030101 0
122041775 12204177 2 20080611 20100317 0
122041775 12204177 3 20120911 0