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
124478622 12447862 2 F 2015 20160810 20160608 20160815 EXP US-BIOGEN-2016BI00248678 BIOGEN 0.00 F Y 0.00000 20160815 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
124478622 12447862 1 PS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION
124478622 12447862 2 SS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124478622 12447862 1 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124478622 12447862 Herpes zoster
124478622 12447862 Multiple sclerosis
124478622 12447862 Pyrexia
124478622 12447862 Renal disorder
124478622 12447862 Respiratory tract infection
124478622 12447862 Sinusitis

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
124478622 12447862 1 20110401 20120703 0
124478622 12447862 2 20141003 20160510 0