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
118633512 11863351 2 F 20160729 20151223 20160803 PER US-BIOGEN-2015BI00162318 BIOGEN 0.00 F Y 0.00000 20160803 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
118633512 11863351 1 PS AVONEX INTERFERON BETA-1A 1 Intramuscular Y 103628 30 UG SOLN FOR INJECT IN PRE-FILLED SYRINGE /wk
118633512 11863351 2 SS AVONEX INTERFERON BETA-1A 1 Intramuscular Y 103628 30 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN /wk
118633512 11863351 3 SS AVONEX INTERFERON BETA-1A 1 Unknown Y 103628 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118633512 11863351 1 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
118633512 11863351 Anxiety
118633512 11863351 Blood cholesterol increased
118633512 11863351 Cataract
118633512 11863351 Cognitive disorder
118633512 11863351 Depression
118633512 11863351 Urticaria

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
118633512 11863351 1 20040319 0
118633512 11863351 2 20130613 0
118633512 11863351 3 20040319 20130613 0