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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124884642 | 12488464 | 2 | F | 201111 | 20160706 | 20160622 | 20160711 | EXP | US-ACORDA-ACO_125209_2016 | ACORDA | 48.00 | YR | M | Y | 0.00000 | 20160711 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124884642 | 12488464 | 1 | PS | AMPYRA | DALFAMPRIDINE | 1 | Oral | 10 MG, BID | Y | U | 22250 | 10 | MG | TABLET | BID | ||||
124884642 | 12488464 | 2 | SS | TIZANIDINE. | TIZANIDINE | 1 | Unknown | U | U | 0 | |||||||||
124884642 | 12488464 | 3 | C | TECFIDERA | DIMETHYL FUMARATE | 1 | Unknown | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
124884642 | 12488464 | 1 | Multiple sclerosis |
124884642 | 12488464 | 2 | Product used for unknown indication |
124884642 | 12488464 | 3 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
124884642 | 12488464 | HO |
124884642 | 12488464 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
124884642 | 12488464 | Contusion | |
124884642 | 12488464 | Fall | |
124884642 | 12488464 | Food poisoning | |
124884642 | 12488464 | Ligament sprain | |
124884642 | 12488464 | Tibia fracture |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |