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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122393298 | 12239329 | 8 | F | 2015 | 20160704 | 20160405 | 20160712 | EXP | BR-ABBVIE-16P-020-1598092-00 | ABBVIE | 62.74 | YR | F | Y | 50.00000 | KG | 20160712 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122393298 | 12239329 | 1 | PS | DEPAKOTE | DIVALPROEX SODIUM | 1 | Oral | U | 1008067,UNKNOWN,1008067 | 19680 | 500 | MG | Q12H | ||||||
| 122393298 | 12239329 | 2 | SS | DEPAKOTE | DIVALPROEX SODIUM | 1 | Oral | U | 1008067,UNKNOWN,1008067 | 19680 | 250 | MG | Q12H | ||||||
| 122393298 | 12239329 | 3 | SS | DEPAKOTE | DIVALPROEX SODIUM | 1 | Oral | U | 1008067,UNKNOWN,1008067 | 19680 | 375 | MG | Q12H | ||||||
| 122393298 | 12239329 | 4 | SS | DEPAKOTE | DIVALPROEX SODIUM | 1 | Unknown | U | 1008067,UNKNOWN,1008067 | 19680 | |||||||||
| 122393298 | 12239329 | 5 | C | MEMANTINE HYDROCHLORIDE. | MEMANTINE HYDROCHLORIDE | 1 | Oral | DAILY DOSE:2 TABLET (IN THE MORNING AND AT NIGHT) | 0 | 1 | DF | BID | |||||||
| 122393298 | 12239329 | 6 | C | RANITIDINE. | RANITIDINE | 1 | 0 | 50 | MG | Q12H |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 122393298 | 12239329 | 1 | Seizure |
| 122393298 | 12239329 | 5 | Dementia Alzheimer's type |
| 122393298 | 12239329 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 122393298 | 12239329 | HO |
| 122393298 | 12239329 | DS |
| 122393298 | 12239329 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 122393298 | 12239329 | Abasia | |
| 122393298 | 12239329 | Anaemia | |
| 122393298 | 12239329 | Hyperhidrosis | |
| 122393298 | 12239329 | Hypotension | |
| 122393298 | 12239329 | Pain | |
| 122393298 | 12239329 | Pneumonia | |
| 122393298 | 12239329 | Pyrexia | |
| 122393298 | 12239329 | Seizure | |
| 122393298 | 12239329 | Somnolence | |
| 122393298 | 12239329 | Urinary tract infection |
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 |
|---|---|---|---|---|---|---|
| 122393298 | 12239329 | 1 | 2015 | 2016 | 0 | |
| 122393298 | 12239329 | 2 | 2011 | 0 | ||
| 122393298 | 12239329 | 3 | 2015 | 0 | ||
| 122393298 | 12239329 | 4 | 20160604 | 0 | ||
| 122393298 | 12239329 | 5 | 2010 | 201509 | 0 |