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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125981082 | 12598108 | 2 | F | 2016 | 20160811 | 20160726 | 20160826 | EXP | US-SAOL THERAPEUTICS-2016SAO00235 | SAOL THERAPEUTICS | 0.00 | M | Y | 0.00000 | 20160826 | CN | COUNTRY NOT SPECIFIED | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125981082 | 12598108 | 1 | PS | LIORESAL | BACLOFEN | 1 | Intrathecal | UNK | Y | 20075 | INJECTION | ||||||||
125981082 | 12598108 | 2 | SS | LIORESAL | BACLOFEN | 1 | Intrathecal | 245.6 ?G, DAY | Y | 20075 | 245.6 | UG | INJECTION | QD | |||||
125981082 | 12598108 | 3 | SS | LIORESAL | BACLOFEN | 1 | Intrathecal | 233.2 ?G, DAY | Y | 20075 | 233.2 | UG | INJECTION | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125981082 | 12598108 | 1 | Multiple sclerosis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125981082 | 12598108 | HO |
125981082 | 12598108 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125981082 | 12598108 | Implant site infection | |
125981082 | 12598108 | Pocket erosion |
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 |
---|---|---|---|---|---|---|
125981082 | 12598108 | 3 | 20160613 | 0 |