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 |