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
125236001 12523600 1 I 201605 20160623 20160703 20160703 PER US-BIOGEN-2016BI00257272 BIOGEN 37.58 YR F Y 64.85000 KG 20160703 CN 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
125236001 12523600 1 PS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) INFUSED OVER 1 HOUR 125104 300 MG UNKNOWN
125236001 12523600 2 C AMPYRA DALFAMPRIDINE 1 Oral 0 10 MG PROLONGED-RELEASE TABLET BID
125236001 12523600 3 C MIRENA LEVONORGESTREL 1 Unknown 0 UNKNOWN
125236001 12523600 4 C DIAZEPAM. DIAZEPAM 1 Unknown 0 5 MG NASAL SPRAY

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125236001 12523600 1 Multiple sclerosis
125236001 12523600 2 Gait disturbance
125236001 12523600 3 Product used for unknown indication
125236001 12523600 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125236001 12523600 Asthenia
125236001 12523600 Cognitive disorder
125236001 12523600 Gait disturbance
125236001 12523600 Hypoaesthesia
125236001 12523600 Loss of control of legs

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
125236001 12523600 1 201501 0
125236001 12523600 2 201503 201605 0
125236001 12523600 3 2013 0
125236001 12523600 4 2010 0