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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126842431 | 12684243 | 1 | I | 20140101 | 20160812 | 20160825 | 20160825 | EXP | GB-MHRA-EYC 00143537 | GB-TEVA-685561ACC | TEVA | 41.00 | YR | F | Y | 69.85000 | KG | 20160825 | CN | GB | GB |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126842431 | 12684243 | 1 | PS | TOPIRAMATE. | TOPIRAMATE | 1 | Oral | NOT KNOWN | Y | U | 76317 | ||||||||
| 126842431 | 12684243 | 2 | C | AMITRIPTYLINE | AMITRIPTYLINE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126842431 | 12684243 | 1 | Hemiplegic migraine |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126842431 | 12684243 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126842431 | 12684243 | Abdominal pain upper | |
| 126842431 | 12684243 | Decreased appetite | |
| 126842431 | 12684243 | Food intolerance | |
| 126842431 | 12684243 | Lethargy | |
| 126842431 | 12684243 | Palpitations |
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 |
|---|---|---|---|---|---|---|
| 126842431 | 12684243 | 1 | 20130301 | 20140401 | 0 |