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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5795552 | 6658051 | F | 5795552-3 | 20080618 | 20080630 | EXP | PHHY2008JP09541 | NOVARTIS PHARMACEUTICALS CORP. | 68 | YR | M | Y | 20080630 | PH | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5795552 | 1010112648 | SS | TERNELIN | 2 | ORAL | UNK | |||||
| 5795552 | 1010112649 | PS | VOLTAREN | 1 | RECTAL | UNK | 019201 | ||||
| 5795552 | 1010112650 | C | AMARYL | 1 | ORAL |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5795552 | 1010112650 | DIABETES MELLITUS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5795552 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5795552 | GLUCOSE URINE PRESENT |
| 5795552 | GLYCOSYLATED HAEMOGLOBIN INCREASED |
| 5795552 | PROTEINURIA |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |