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
125385471 12538547 1 I 2016 20160630 20160708 20160708 PER US-BIOGEN-2016BI00260924 BIOGEN 55.09 YR F Y 0.00000 20160708 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
125385471 12538547 1 PS AVONEX INTERFERON BETA-1A 1 Intramuscular PT DID NOT HAVE LOT #S 103628 30 UG POWDER FOR SOLUTION FOR INJECTION /wk
125385471 12538547 2 SS AVONEX INTERFERON BETA-1A 1 Intramuscular PT DID NOT HAVE LOT #S 103628 30 UG POWDER FOR SOLUTION FOR INJECTION /wk
125385471 12538547 3 SS AVONEX INTERFERON BETA-1A 1 Intramuscular PT DID NOT HAVE LOT #S 103628 30 UG POWDER FOR SOLUTION FOR INJECTION /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125385471 12538547 1 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125385471 12538547 Headache
125385471 12538547 Influenza like illness
125385471 12538547 Nuclear magnetic resonance imaging abnormal

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
125385471 12538547 1 19960501 0
125385471 12538547 2 19991102 0
125385471 12538547 3 20160422 0