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
125908401 12590840 1 I 20160722 20160726 20160726 PER US-BIOGEN-2016BI00269916 BIOGEN 0.00 F Y 0.00000 20160726 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
125908401 12590840 1 PS PLEGRIDY PEGINTERFERON BETA-1A 1 Unknown 125499 UNKNOWN
125908401 12590840 2 SS TECFIDERA DIMETHYL FUMARATE 1 Unknown U 204063 UNKNOWN
125908401 12590840 3 SS AVONEX INTERFERON BETA-1A 1 Unknown U 103628 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125908401 12590840 1 Multiple sclerosis
125908401 12590840 2 Multiple sclerosis
125908401 12590840 3 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125908401 12590840 Asthenia
125908401 12590840 Balance disorder
125908401 12590840 Coordination abnormal
125908401 12590840 Malaise
125908401 12590840 Mobility decreased
125908401 12590840 Nausea

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
125908401 12590840 1 20160608 0
125908401 12590840 2 20140828 0
125908401 12590840 3 19991212 20160502 0