Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5688586 | 6601560 | I | 5688586-0 | 20080220 | 20080319 | 20080331 | EXP | PHHY2008JP03620 | NOVARTIS PHARMACEUTICALS CORP. | 80 | YR | F | Y | 20080329 | MD | JAPAN |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5688586 | 1009725586 | PS | NEORAL | 1 | ORAL | 325 MG/ DAY | 050715 | ||||
| 5688586 | 1009725587 | C | DRUG THERAPY NOS | 2 | 5 MG/DAY | ||||||
| 5688586 | 1009725588 | C | DRUG THERAPY NOS | 2 | 10 MG/DAY |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5688586 | 1009725586 | PEMPHIGOID |
| 5688586 | 1009725587 | PEMPHIGOID |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5688586 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5688586 | GAIT DISTURBANCE |
| 5688586 | HEPATIC FUNCTION ABNORMAL |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 5688586 | 1009725586 | 20080101 | 20080225 | ||
| 5688586 | 1009725587 | 20070101 |