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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 98953726 | 9895372 | 6 | F | 20140202 | 20160913 | 20140213 | 20160927 | EXP | US-ACORDA-ACO_101701_2014 | ACORDA | 61.57 | YR | F | Y | 58.50000 | KG | 20160927 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 98953726 | 9895372 | 1 | PS | AMPYRA | DALFAMPRIDINE | 1 | Oral | 10 MG, BID | 17760 | MG | Y | N | 22250 | 10 | MG | TABLET | BID | ||
| 98953726 | 9895372 | 2 | SS | AMPYRA | DALFAMPRIDINE | 1 | Oral | UNK | 17760 | MG | Y | N | 22250 | TABLET | |||||
| 98953726 | 9895372 | 3 | SS | COPAXONE | GLATIRAMER ACETATE | 1 | Unknown | 20 MG, UNK | 0 | 20 | MG | ||||||||
| 98953726 | 9895372 | 4 | I | Other therapeutic products | UNSPECIFIED INGREDIENT | 1 | Unknown | UNK | Y | 0 | |||||||||
| 98953726 | 9895372 | 5 | SS | PROVIGIL | MODAFINIL | 1 | Unknown | UNK | 0 | ||||||||||
| 98953726 | 9895372 | 6 | C | TOPIRAMATE. | TOPIRAMATE | 1 | Unknown | UNK | U | 0 | |||||||||
| 98953726 | 9895372 | 7 | C | Calcium | CALCIUM | 1 | Unknown | UNK | U | 0 | |||||||||
| 98953726 | 9895372 | 8 | C | ALLERGY MEDICATION | DIPHENHYDRAMINE HYDROCHLORIDE | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 98953726 | 9895372 | 1 | Multiple sclerosis |
| 98953726 | 9895372 | 2 | Gait disturbance |
| 98953726 | 9895372 | 3 | Multiple sclerosis |
| 98953726 | 9895372 | 4 | Affective disorder |
| 98953726 | 9895372 | 5 | Product used for unknown indication |
| 98953726 | 9895372 | 6 | Product used for unknown indication |
| 98953726 | 9895372 | 7 | Product used for unknown indication |
| 98953726 | 9895372 | 8 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 98953726 | 9895372 | HO |
| 98953726 | 9895372 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 98953726 | 9895372 | Accidental overdose | |
| 98953726 | 9895372 | Contraindicated product administered | |
| 98953726 | 9895372 | Drug interaction | |
| 98953726 | 9895372 | Feeling hot | |
| 98953726 | 9895372 | Gait disturbance | |
| 98953726 | 9895372 | Impaired work ability | |
| 98953726 | 9895372 | Product selection error | |
| 98953726 | 9895372 | Seizure | |
| 98953726 | 9895372 | Somnolence | |
| 98953726 | 9895372 | Syncope | |
| 98953726 | 9895372 | Weight fluctuation |
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 |
|---|---|---|---|---|---|---|
| 98953726 | 9895372 | 1 | 20110830 | 20140202 | 0 | |
| 98953726 | 9895372 | 3 | 20020403 | 0 | ||
| 98953726 | 9895372 | 4 | 2016 | 0 |