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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125802272 | 12580227 | 2 | F | 20160816 | 20160721 | 20160822 | EXP | FR-UCBSA-2016026573 | UCB | RAMON M, TOURTEAU E, LEMAIRE N, GAUTIER S, BENE J. HYPERCKEMIA INDUCED BY LEVETIRACETAM. PRESSE MED. 2016 | 25.00 | YR | M | Y | 0.00000 | 20160822 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125802272 | 12580227 | 1 | PS | KEPPRA | LEVETIRACETAM | 1 | UNKNOWN DOSE | Y | 21035 | ||||||||||
| 125802272 | 12580227 | 2 | SS | KEPPRA | LEVETIRACETAM | 1 | 500 MG, 2X/DAY (BID) | Y | 21035 | 500 | MG | BID | |||||||
| 125802272 | 12580227 | 3 | C | CLONAZEPAM. | CLONAZEPAM | 1 | 1 MG, 2X/DAY (BID) | U | 0 | 1 | MG | BID | |||||||
| 125802272 | 12580227 | 4 | C | FOSPHENYTOIN | FOSPHENYTOINFOSPHENYTOIN SODIUM | 1 | 1.5 G | U | 0 | ||||||||||
| 125802272 | 12580227 | 5 | C | Thiopental | THIOPENTAL | 1 | UNKNOWN DOSE | U | 0 | INFUSION | |||||||||
| 125802272 | 12580227 | 6 | C | Thiopental | THIOPENTAL | 1 | UNKNOWN DOSE | U | 0 | INFUSION | |||||||||
| 125802272 | 12580227 | 7 | C | Sufentanil | SUFENTANIL | 1 | UNKNOWN DOSE | U | 0 | ||||||||||
| 125802272 | 12580227 | 8 | C | Clobazam | CLOBAZAM | 1 | 5 MG, 3X/DAY (TID) ON DAY 1 | Y | 0 | 5 | MG | TID | |||||||
| 125802272 | 12580227 | 9 | C | Clobazam | CLOBAZAM | 1 | DECREASED TO 5 MG TWICE DAILY (DAY 4) | Y | 0 | 5 | MG | BID | |||||||
| 125802272 | 12580227 | 10 | C | Esomeprazole | ESOMEPRAZOLE | 1 | 40 MG | Y | 0 | 40 | MG | ||||||||
| 125802272 | 12580227 | 11 | C | PROPOFOL. | PROPOFOL | 1 | UNKNOWN DOSE | Y | 0 | ||||||||||
| 125802272 | 12580227 | 12 | C | Enoxaparin | ENOXAPARIN | 1 | UNKNOWN DOSE | U | 0 | ||||||||||
| 125802272 | 12580227 | 13 | C | Suxamethonium | SUCCINYLCHOLINE | 1 | UNKNOWN DOSE | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125802272 | 12580227 | 1 | Epilepsy |
| 125802272 | 12580227 | 3 | Seizure |
| 125802272 | 12580227 | 4 | Seizure |
| 125802272 | 12580227 | 5 | Seizure |
| 125802272 | 12580227 | 6 | Status epilepticus |
| 125802272 | 12580227 | 7 | Status epilepticus |
| 125802272 | 12580227 | 8 | Product used for unknown indication |
| 125802272 | 12580227 | 10 | Product used for unknown indication |
| 125802272 | 12580227 | 11 | Product used for unknown indication |
| 125802272 | 12580227 | 12 | Product used for unknown indication |
| 125802272 | 12580227 | 13 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125802272 | 12580227 | OT |
| 125802272 | 12580227 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125802272 | 12580227 | Blood creatine phosphokinase increased | |
| 125802272 | 12580227 | Insomnia | |
| 125802272 | 12580227 | Status epilepticus |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |