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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125720691 | 12572069 | 1 | I | 20160713 | 20160719 | 20160719 | EXP | PHHY2016SE098276 | NOVARTIS | 54.00 | YR | F | Y | 0.00000 | 20160719 | CN | SE | SE |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125720691 | 12572069 | 1 | PS | TEGRETOL | CARBAMAZEPINE | 1 | Unknown | U | 20234 | EXTENDED RELEASE TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125720691 | 12572069 | 1 | Facial spasm |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125720691 | 12572069 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125720691 | 12572069 | Drug ineffective for unapproved indication | |
125720691 | 12572069 | Mental impairment | |
125720691 | 12572069 | Product use issue |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |