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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127887471 | 12788747 | 1 | I | 20130710 | 20131216 | 20160928 | 20160928 | EXP | DE-UCBSA-108572 | UCB | 71.53 | YR | M | Y | 74.00000 | KG | 20160928 | MD | DE | DE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127887471 | 12788747 | 1 | PS | KEPPRA | LEVETIRACETAM | 1 | STRENGTH:500 ;2X2 PER DAY | D | 21035 | 1000 | MG | BID | |||||||
| 127887471 | 12788747 | 2 | SS | KEPPRA | LEVETIRACETAM | 1 | WAS TAPERED OFF STEP BY STEP | D | 21035 | ||||||||||
| 127887471 | 12788747 | 3 | C | METOPROLOL SUCCINATE. | METOPROLOL SUCCINATE | 1 | Oral | 1X1 | U | 0 | |||||||||
| 127887471 | 12788747 | 4 | C | RAMIPRIL. | RAMIPRIL | 1 | 1X1 | U | 0 | ||||||||||
| 127887471 | 12788747 | 5 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Oral | 1X1 | U | 0 | |||||||||
| 127887471 | 12788747 | 6 | C | Ramipril Piretanid | 2 | Oral | 1X1 | U | 0 | ||||||||||
| 127887471 | 12788747 | 7 | C | Nephrotrans | SODIUM BICARBONATE | 1 | 480, 3X/DAY (TID) | U | 0 | TID | |||||||||
| 127887471 | 12788747 | 8 | C | ARIXTRA | FONDAPARINUX SODIUM | 1 | 2.5 MG, ONCE DAILY (QD) | U | 0 | 2.5 | MG | QD | |||||||
| 127887471 | 12788747 | 9 | C | Nifical | 2 | UNK | U | 0 | |||||||||||
| 127887471 | 12788747 | 10 | C | Tationil | 2 | Intravenous (not otherwise specified) | 600 MG/4 ML | U | 0 | ||||||||||
| 127887471 | 12788747 | 11 | C | Digitoxin | DIGITOXIN | 1 | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127887471 | 12788747 | 1 | Seizure |
| 127887471 | 12788747 | 3 | Product used for unknown indication |
| 127887471 | 12788747 | 4 | Product used for unknown indication |
| 127887471 | 12788747 | 5 | Product used for unknown indication |
| 127887471 | 12788747 | 6 | Product used for unknown indication |
| 127887471 | 12788747 | 7 | Product used for unknown indication |
| 127887471 | 12788747 | 8 | Product used for unknown indication |
| 127887471 | 12788747 | 9 | Product used for unknown indication |
| 127887471 | 12788747 | 11 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127887471 | 12788747 | OT |
| 127887471 | 12788747 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127887471 | 12788747 | Atrial fibrillation | |
| 127887471 | 12788747 | Dizziness | |
| 127887471 | 12788747 | Nocturia |
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 |
|---|---|---|---|---|---|---|
| 127887471 | 12788747 | 1 | 201311 | 0 | ||
| 127887471 | 12788747 | 2 | 201311 | 201312 | 0 |