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
123384832 12338483 2 F 200706 20160620 20160505 20160701 EXP BR-BIOGEN-2016BI00231734 BIOGEN 34.85 YR M Y 0.00000 20160701 MD BR BR

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
123384832 12338483 1 PS AVONEX INTERFERON BETA-1A 1 Intramuscular 103628 30 UG UNKNOWN /wk
123384832 12338483 2 SS AVONEX INTERFERON BETA-1A 1 Unknown 103628 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123384832 12338483 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
123384832 12338483 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123384832 12338483 Headache
123384832 12338483 Malaise
123384832 12338483 Multiple sclerosis relapse
123384832 12338483 Muscle spasms
123384832 12338483 Pyrexia
123384832 12338483 Somnolence

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
123384832 12338483 1 200706 201603 0