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
125432362 12543236 2 F 20160728 20160711 20160801 EXP US-BIOGEN-2016BI00236688 BIOGEN 0.00 F Y 84.44000 KG 20160801 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
125432362 12543236 1 PS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) U 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION
125432362 12543236 2 C GILENYA FINGOLIMOD HYDROCHLORIDE 1 Oral 0 .5 MG UNKNOWN
125432362 12543236 3 C VITAMIN D3 CHOLECALCIFEROL 1 Oral 0 5000 IU UNKNOWN QD
125432362 12543236 4 C VITAMIN D3 CHOLECALCIFEROL 1 Oral 0 10000 IU UNKNOWN QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125432362 12543236 1 Multiple sclerosis
125432362 12543236 2 Product used for unknown indication
125432362 12543236 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125432362 12543236 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125432362 12543236 Abortion spontaneous
125432362 12543236 Maternal exposure during pregnancy

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
125432362 12543236 1 20160322 20160419 0