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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126087331 | 12608733 | 1 | I | 2015 | 20160722 | 20160729 | 20160729 | EXP | BR-ABBVIE-16P-020-1689516-00 | ABBVIE | 0.00 | F | Y | 0.00000 | 20160729 | CN | BR | BR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126087331 | 12608733 | 1 | PS | DEPAKOTE | DIVALPROEX SODIUM | 1 | Oral | DAILY DOSE:250MG AT NIGHT | UNKNOWN | 18723 | 250 | MG | QD | ||||||
| 126087331 | 12608733 | 2 | SS | DEPAKOTE | DIVALPROEX SODIUM | 1 | Oral | UNKNOWN | 18723 | 250 | MG | QOD | |||||||
| 126087331 | 12608733 | 3 | C | RIVOTRIL | CLONAZEPAM | 1 | Oral | DAILY DOSE:1 TABLET AT AFTERNOON | 0 | 1 | DF | QD | |||||||
| 126087331 | 12608733 | 4 | C | AMITRIPTYLINE | AMITRIPTYLINE | 1 | Oral | DAILY DOSE:25 MG AT NIGHT | 0 | 25 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126087331 | 12608733 | 1 | Vein disorder |
| 126087331 | 12608733 | 2 | Memory impairment |
| 126087331 | 12608733 | 3 | Epilepsy |
| 126087331 | 12608733 | 4 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126087331 | 12608733 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126087331 | 12608733 | Fall | |
| 126087331 | 12608733 | Foot fracture | |
| 126087331 | 12608733 | Hemiplegia | |
| 126087331 | 12608733 | Incorrect dose administered | |
| 126087331 | 12608733 | Product supply issue | |
| 126087331 | 12608733 | Product use issue |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |