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
122330804 12233080 4 F 20160809 20160403 20160811 EXP US-BIOGEN-2016BI00211688 BIOGEN 0.00 M Y 0.00000 20160811 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
122330804 12233080 1 PS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION
122330804 12233080 2 SS TYSABRI NATALIZUMAB 1 Unknown 125104 UNKNOWN
122330804 12233080 3 SS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION /month

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122330804 12233080 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
122330804 12233080 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
122330804 12233080 Clostridium difficile infection
122330804 12233080 Decubitus ulcer
122330804 12233080 Pyrexia
122330804 12233080 Urinary tract infection

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
122330804 12233080 1 201203 201506 0
122330804 12233080 2 20140206 0
122330804 12233080 3 20160429 0