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
125282781 12528278 1 I 20160614 20160614 20160705 20160705 EXP CA-BIOGEN-2016BI00253930 BIOGEN 23.48 YR F Y 0.00000 20160705 MD CA CA

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
125282781 12528278 1 PS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) INFUSED OVER ONE HOUR U 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125282781 12528278 1 Relapsing-remitting multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
125282781 12528278 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125282781 12528278 Chest pain
125282781 12528278 Dizziness
125282781 12528278 Fatigue
125282781 12528278 Hypersensitivity
125282781 12528278 Nausea
125282781 12528278 Pain in extremity
125282781 12528278 Pruritus
125282781 12528278 Vision blurred

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
125282781 12528278 1 20151117 20160614 0