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
118855332 11885533 2 F 20151203 20160915 20160104 20160928 PER US-BIOGEN-2015BI00164334 BIOGEN 32.13 YR F Y 0.00000 20160928 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
118855332 11885533 1 PS AVONEX INTERFERON BETA-1A 1 Unknown Y 103628 UNKNOWN
118855332 11885533 2 SS AVONEX INTERFERON BETA-1A 1 Intramuscular Y 103628 30 UG UNKNOWN /wk
118855332 11885533 3 C VITAMIN D3 CHOLECALCIFEROL 1 Unknown 0 UNKNOWN
118855332 11885533 4 C NORTRIPTYLINE NORTRIPTYLINE 1 Unknown 0 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118855332 11885533 1 Multiple sclerosis
118855332 11885533 3 Product used for unknown indication
118855332 11885533 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
118855332 11885533 General symptom
118855332 11885533 Headache
118855332 11885533 Multiple sclerosis relapse
118855332 11885533 Treatment failure

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
118855332 11885533 1 20150417 0
118855332 11885533 2 201503 20151201 0