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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125924791 | 12592479 | 1 | I | 20160712 | 20160726 | 20160726 | EXP | US-ACORDA-ACO_126270_2016 | ACORDA | 0.00 | F | Y | 0.00000 | 20160726 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125924791 | 12592479 | 1 | PS | AMPYRA | DALFAMPRIDINE | 1 | Oral | 10 MG, BID | 22250 | 10 | MG | TABLET | BID |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125924791 | 12592479 | 1 | Gait disturbance |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125924791 | 12592479 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125924791 | 12592479 | Balance disorder | |
125924791 | 12592479 | Blood glucose decreased | |
125924791 | 12592479 | Fall | |
125924791 | 12592479 | Hypertension | |
125924791 | 12592479 | Inappropriate schedule of drug administration | |
125924791 | 12592479 | Jaw fracture |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |