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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126709961 | 12670996 | 1 | I | 20160808 | 20160822 | 20160822 | EXP | HK-ACCORD-043292 | ACCORD | YEUNG TL, LI PS, LI KK. PRESUMED TOPIRAMATE RETINOPATHY: A CASE REPORT. J MED CASE REP. 2016 AUG 1;10:210. | 48.00 | YR | F | Y | 0.00000 | 20160822 | OT | HK | HK |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126709961 | 12670996 | 1 | PS | TOPIRAMATE. | TOPIRAMATE | 1 | 26 MONTHS AFTER VALPROATE; INITIAL DOSE WAS 25 MG TWICE A DAY THEN STEPPED UP TO 100 MG TWICE A DAY | Y | 76311 | 100 | MG | BID |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126709961 | 12670996 | 1 | Seizure |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126709961 | 12670996 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126709961 | 12670996 | Retinopathy | |
126709961 | 12670996 | Toxicity to various agents | |
126709961 | 12670996 | Visual field defect |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |