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
122770183 12277018 3 F 2015 20160708 20160418 20160719 EXP GB-BIOGEN-2016BI00217139 BIOGEN 0.00 F Y 0.00000 20160719 OT GB GB

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
122770183 12277018 1 PS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) 6895 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION
122770183 12277018 2 C KEPPRA LEVETIRACETAM 1 Unknown 0 500 MG UNKNOWN
122770183 12277018 3 C GABAPENTIN. GABAPENTIN 1 Unknown 0 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122770183 12277018 1 Relapsing-remitting multiple sclerosis
122770183 12277018 2 Product used for unknown indication
122770183 12277018 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
122770183 12277018 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122770183 12277018 Gait disturbance
122770183 12277018 Mobility decreased
122770183 12277018 Seizure

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
122770183 12277018 1 201406 20160414 0