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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125721361 | 12572136 | 1 | I | 20160311 | 20160718 | 20160719 | 20160719 | EXP | PHHY2016CN098825 | NOVARTIS | 42.52 | YR | F | Y | 55.00000 | KG | 20160719 | OT | CN | CN |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125721361 | 12572136 | 1 | PS | TEGRETOL | CARBAMAZEPINE | 1 | Oral | 1 DF, BID | 26 | DF | Y | X0904 | 16608 | 1 | DF | TABLET | BID |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125721361 | 12572136 | 1 | Pain |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125721361 | 12572136 | HO |
125721361 | 12572136 | LT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125721361 | 12572136 | Mouth ulceration | |
125721361 | 12572136 | Pyrexia | |
125721361 | 12572136 | Rash |
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 |
---|---|---|---|---|---|---|
125721361 | 12572136 | 1 | 20160228 | 20160311 | 0 |