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
99038383 9903838 3 F 1998 20140211 20140218 20151001 PER US-BIOGENIDEC-2014BI014892 BIOGEN 0.00 M Y 0.00000 20151001 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
99038383 9903838 1 PS AVONEX INTERFERON BETA-1A 1 Intramuscular 103628 30 UG /wk
99038383 9903838 2 SS AVONEX INTERFERON BETA-1A 1 Intramuscular 103628 30 UG SOLUTION FOR INJECTION /wk
99038383 9903838 3 SS AVONEX INTERFERON BETA-1A 1 Intramuscular 103628 30 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
99038383 9903838 1 Multiple sclerosis
99038383 9903838 2 Multiple sclerosis
99038383 9903838 3 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
99038383 9903838 Feeling abnormal
99038383 9903838 Ill-defined disorder
99038383 9903838 Influenza like illness
99038383 9903838 Pain
99038383 9903838 Vision blurred

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
99038383 9903838 1 1997 0
99038383 9903838 2 19980101 20140430 0
99038383 9903838 3 20150923 0