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
79612579 7961257 9 F 201105 20121218 20110526 20121231 EXP FR-BIOGENIDEC-2011BI018509 BIOGEN 33.00 YR M Y 0.00000 20121231 OT FR FR

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
79612579 7961257 1 PS TYSABRI 1 INTRAVENOUS D 125104 300 MG Intravenous infusion /month

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
79612579 7961257 1 Relapsing-remitting multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
79612579 7961257 DS
79612579 7961257 HO
79612579 7961257 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
79612579 7961257 Immune reconstitution inflammatory syndrome
79612579 7961257 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
79612579 7961257 1 200905 201104 0