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
121715984 12171598 4 F 20160111 20160803 20160311 20160812 EXP CO-BIOGEN-2016BI00179939 BIOGEN 26.70 YR F Y 75.00000 KG 20160812 CN CO CO

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
121715984 12171598 1 PS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) U 125104 300 MG UNKNOWN
121715984 12171598 2 SS TYSABRI NATALIZUMAB 1 Unknown U 125104 UNKNOWN
121715984 12171598 3 SS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) U 125104 300 MG UNKNOWN
121715984 12171598 4 SS FAMPYRA DALFAMPRIDINE 1 Unknown U 22250 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121715984 12171598 1 Multiple sclerosis
121715984 12171598 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
121715984 12171598 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
121715984 12171598 Feeling hot
121715984 12171598 Hypersensitivity
121715984 12171598 Hypotonia
121715984 12171598 Multiple sclerosis relapse
121715984 12171598 Pain
121715984 12171598 Pain in extremity
121715984 12171598 Viral 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
121715984 12171598 1 201512 201601 0
121715984 12171598 2 201602 0
121715984 12171598 3 201605 0