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
124347422 12434742 2 F 20160630 20160603 20160706 EXP US-BIOGEN-2016BI00246398 BIOGEN 0.00 F Y 0.00000 20160706 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
124347422 12434742 1 PS AVONEX INTERFERON BETA-1A 1 Unknown 103628 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124347422 12434742 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
124347422 12434742 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124347422 12434742 Deafness
124347422 12434742 Influenza like illness
124347422 12434742 Pain in extremity

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
124347422 12434742 1 20100325 0