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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124137122 | 12413712 | 2 | F | 2016 | 20160518 | 20160527 | 20160830 | PER | US-SUPERNUS PHARMACEUTICALS, INC.-2016SUP00077 | SUPERNUS | 0.00 | F | Y | 50.34000 | KG | 20160830 | CN | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124137122 | 12413712 | 1 | PS | TROKENDI XR | TOPIRAMATE | 1 | Oral | 50 MG, 1X/DAY | Y | 201635 | 50 | MG | PROLONGED-RELEASE TABLET | QD | |||||
| 124137122 | 12413712 | 2 | SS | TROKENDI XR | TOPIRAMATE | 1 | Oral | 150 MG, 1X/DAY | Y | 201635 | 150 | MG | PROLONGED-RELEASE TABLET | QD | |||||
| 124137122 | 12413712 | 3 | SS | TROKENDI XR | TOPIRAMATE | 1 | Oral | 100 MG, 1X/DAY | Y | 201635 | 100 | MG | PROLONGED-RELEASE TABLET | QD | |||||
| 124137122 | 12413712 | 4 | SS | TROKENDI XR | TOPIRAMATE | 1 | UNK | Y | 201635 | PROLONGED-RELEASE TABLET | |||||||||
| 124137122 | 12413712 | 5 | SS | LAMICTAL | LAMOTRIGINE | 1 | UNK | U | U | 0 | |||||||||
| 124137122 | 12413712 | 6 | SS | LEVOTHYROXINE. | LEVOTHYROXINE | 1 | UNK | Y | 0 | ||||||||||
| 124137122 | 12413712 | 7 | C | ^TRIVLAR^ | 2 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124137122 | 12413712 | 1 | Seizure |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124137122 | 12413712 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124137122 | 12413712 | Decreased appetite | |
| 124137122 | 12413712 | Depression | |
| 124137122 | 12413712 | Dizziness | |
| 124137122 | 12413712 | Drug interaction | |
| 124137122 | 12413712 | Memory impairment | |
| 124137122 | 12413712 | Nausea | |
| 124137122 | 12413712 | Palpitations | |
| 124137122 | 12413712 | Seizure | |
| 124137122 | 12413712 | Therapeutic response decreased | |
| 124137122 | 12413712 | Weight decreased |
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 |
|---|---|---|---|---|---|---|
| 124137122 | 12413712 | 1 | 201602 | 2016 | 0 | |
| 124137122 | 12413712 | 2 | 2016 | 2016 | 0 | |
| 124137122 | 12413712 | 3 | 2016 | 201603 | 0 | |
| 124137122 | 12413712 | 5 | 201603 | 0 | ||
| 124137122 | 12413712 | 6 | 201603 | 0 |