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
102828974 10282897 4 F 201406 20150618 20140708 20150630 EXP US-BIOGENIDEC-2014BI061515 BIOGEN 57.00 YR A F Y 0.00000 20150630 N OT 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
102828974 10282897 1 PS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) D 125104 300 MG INTRAVENOUS INFUSION /month
102828974 10282897 2 SS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) D 125104 300 MG INTRAVENOUS INFUSION /month

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
102828974 10282897 1 Multiple sclerosis
102828974 10282897 2 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
102828974 10282897 OT
102828974 10282897 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
102828974 10282897 Immune reconstitution inflammatory syndrome
102828974 10282897 Progressive multifocal leukoencephalopathy

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
102828974 10282897 1 20110422 20130401 0
102828974 10282897 2 20130520 20140519 0