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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126964431 | 12696443 | 1 | I | 20160823 | 20160830 | 20160830 | EXP | FR-UCBSA-2016032839 | UCB | 88.00 | YR | M | Y | 0.00000 | 20160830 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126964431 | 12696443 | 1 | PS | Xyzall | LEVOCETIRIZINE DIHYDROCHLORIDE | 1 | Oral | UNK | Y | U | 22064 | ||||||||
| 126964431 | 12696443 | 2 | SS | Seroplex | ESCITALOPRAM OXALATE | 1 | Oral | 5 MG, ONCE DAILY (QD) | Y | U | 0 | 5 | MG | QD | |||||
| 126964431 | 12696443 | 3 | SS | Esomeprazole | ESOMEPRAZOLE | 1 | Oral | 20 MG, ONCE DAILY (QD) | Y | U | 0 | 20 | MG | QD | |||||
| 126964431 | 12696443 | 4 | SS | ALPRAZOLAM. | ALPRAZOLAM | 1 | Oral | 0.5 MG, ONCE DAILY (QD) | Y | U | 0 | .5 | MG | QD | |||||
| 126964431 | 12696443 | 5 | C | Amlor | AMLODIPINE BESYLATE | 1 | Oral | 5 MG, ONCE DAILY (QD) | U | 0 | 5 | MG | QD | ||||||
| 126964431 | 12696443 | 6 | C | Aprovel | IRBESARTAN | 1 | Oral | 300 MG, ONCE DAILY (QD) | U | 0 | 300 | MG | ORAL DROPS | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126964431 | 12696443 | 1 | Product used for unknown indication |
| 126964431 | 12696443 | 2 | Depression |
| 126964431 | 12696443 | 3 | Product used for unknown indication |
| 126964431 | 12696443 | 4 | Depression |
| 126964431 | 12696443 | 5 | Hypertension |
| 126964431 | 12696443 | 6 | Hypertension |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126964431 | 12696443 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126964431 | 12696443 | 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 |
|---|---|---|---|---|---|---|
| 126964431 | 12696443 | 1 | 201607 | 0 | ||
| 126964431 | 12696443 | 2 | 20160722 | 0 | ||
| 126964431 | 12696443 | 3 | 20160722 | 0 | ||
| 126964431 | 12696443 | 4 | 201607 | 0 |