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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125421832 | 12542183 | 2 | F | 2014 | 20160816 | 20160708 | 20160919 | EXP | DK-SAOL THERAPEUTICS-2016SAO00098 | SAOL THERAPEUTICS | 39.00 | YR | M | Y | 0.00000 | 20160919 | CN | COUNTRY NOT SPECIFIED | DK |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125421832 | 12542183 | 1 | PS | LIORESAL | BACLOFEN | 1 | 290 ?G, DAY | U | U | 20075 | 290 | UG | INJECTION | QD | |||||
| 125421832 | 12542183 | 2 | SS | LIORESAL | BACLOFEN | 1 | U | U | 20075 | INJECTION |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125421832 | 12542183 | 1 | Multiple sclerosis |
| 125421832 | 12542183 | 2 | Muscle spasticity |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125421832 | 12542183 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125421832 | 12542183 | Device issue | |
| 125421832 | 12542183 | Implant site infection | |
| 125421832 | 12542183 | Muscle spasticity | |
| 125421832 | 12542183 | Therapy non-responder |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |