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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
120601702 | 12060170 | 2 | F | 201512 | 20160912 | 20160210 | 20160922 | EXP | GB-MHRA-EYC 00134185 | GB-TEVA-631576ACC | TEVA | 15.00 | YR | F | Y | 0.00000 | 20160922 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
120601702 | 12060170 | 1 | PS | TOPIRAMATE. | TOPIRAMATE | 1 | Oral | 100 MILLIGRAM DAILY; | Y | U | 76317 | 50 | MG | BID |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
120601702 | 12060170 | 1 | Migraine |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
120601702 | 12060170 | OT |
120601702 | 12060170 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
120601702 | 12060170 | Central nervous system lesion | |
120601702 | 12060170 | Headache | |
120601702 | 12060170 | Noninfective encephalitis | |
120601702 | 12060170 | Vomiting |
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 |
---|---|---|---|---|---|---|
120601702 | 12060170 | 1 | 201509 | 201512 | 0 |