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
125039473 12503947 3 F 201304 20160729 20160628 20160804 EXP US-BIOGEN-2013BI064479 BIOGEN 60.93 YR M Y 0.00000 20160804 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
125039473 12503947 1 PS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) INFUSED OVER 1 HOUR U 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION
125039473 12503947 2 SS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) INFUSED OVER 1 HOUR U 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION
125039473 12503947 3 C WARFARIN WARFARIN 1 Unknown 0 UNKNOWN
125039473 12503947 4 C WARFARIN WARFARIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125039473 12503947 1 Multiple sclerosis
125039473 12503947 3 Pulmonary thrombosis
125039473 12503947 4 Urinary bladder haemorrhage

Outcome of event

Event ID CASEID OUTC COD
125039473 12503947 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125039473 12503947 Dyspnoea
125039473 12503947 Infection
125039473 12503947 Loss of control of legs
125039473 12503947 Malaise
125039473 12503947 Pulmonary thrombosis
125039473 12503947 Urinary bladder haemorrhage

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
125039473 12503947 1 20090402 20130425 0
125039473 12503947 2 20130820 0