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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127092201 | 12709220 | 1 | I | 20160125 | 20160824 | 20160901 | 20160901 | EXP | FR-ABBVIE-16P-056-1715139-00 | ABBVIE | 39.00 | YR | M | Y | 0.00000 | 20160901 | OT | FR | FR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127092201 | 12709220 | 1 | PS | DEPAKINE CHRONO | VALPROATE SODIUM | 1 | Oral | EXTENDED RELEASE | UNKNOWN | 18081 | 2 | DF | TABLET | BID | |||||
| 127092201 | 12709220 | 2 | SS | TEGRETOL | CARBAMAZEPINE | 1 | Oral | UNKNOWN | 0 | 1 | DF | TABLET | BID | ||||||
| 127092201 | 12709220 | 3 | SS | AOTAL | ACAMPROSATE CALCIUM | 1 | Oral | UNKNOWN | 0 | 4 | DF | GASTRO-RESISTANT TABLET | QD | ||||||
| 127092201 | 12709220 | 4 | SS | SERESTA | OXAZEPAM | 1 | Oral | 0 | 1 | DF | BID | ||||||||
| 127092201 | 12709220 | 5 | C | NAPROXEN. | NAPROXEN | 1 | 0 | ||||||||||||
| 127092201 | 12709220 | 6 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | 0 | ||||||||||||
| 127092201 | 12709220 | 7 | C | METEOSPASMYL | ALVERINE CITRATEDIMETHICONE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127092201 | 12709220 | 1 | Epilepsy |
| 127092201 | 12709220 | 2 | Epilepsy |
| 127092201 | 12709220 | 3 | Alcohol detoxification |
| 127092201 | 12709220 | 4 | Sedative therapy |
| 127092201 | 12709220 | 5 | Product used for unknown indication |
| 127092201 | 12709220 | 6 | Product used for unknown indication |
| 127092201 | 12709220 | 7 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127092201 | 12709220 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127092201 | 12709220 | Hyperkalaemia | |
| 127092201 | 12709220 | Hyponatraemia |
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 |
|---|---|---|---|---|---|---|
| 127092201 | 12709220 | 1 | 1999 | 0 | ||
| 127092201 | 12709220 | 2 | 1999 | 0 | ||
| 127092201 | 12709220 | 3 | 20160111 | 0 | ||
| 127092201 | 12709220 | 4 | 20160111 | 0 | ||
| 127092201 | 12709220 | 5 | 20160125 | 20160125 | 0 | |
| 127092201 | 12709220 | 6 | 20160125 | 20160125 | 0 | |
| 127092201 | 12709220 | 7 | 20160125 | 20160125 | 0 |