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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126653481 | 12665348 | 1 | I | 201106 | 20110627 | 20160818 | 20160818 | EXP | US-SAOL THERAPEUTICS-2016SAO00414 | SAOL THERAPEUTICS | 54.45 | YR | M | Y | 0.00000 | 20160818 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126653481 | 12665348 | 1 | PS | COMPOUNDED BACLOFEN | BACLOFEN | 1 | U | U | 20075 | INJECTION | |||||||||
| 126653481 | 12665348 | 2 | SS | MORPHINE | MORPHINE | 1 | Intrathecal | U | 0 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126653481 | 12665348 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126653481 | 12665348 | Blister | |
| 126653481 | 12665348 | Bradycardia | |
| 126653481 | 12665348 | Device malfunction | |
| 126653481 | 12665348 | Drug withdrawal syndrome | |
| 126653481 | 12665348 | Headache | |
| 126653481 | 12665348 | Hyperhidrosis | |
| 126653481 | 12665348 | Lethargy | |
| 126653481 | 12665348 | Nausea | |
| 126653481 | 12665348 | Overdose | |
| 126653481 | 12665348 | Pain |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |