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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4542786 | 5706632 | I | 4542786-1 | 20040901 | 20041227 | 20041231 | EXP | PHHO2004JP18430 | NOVARTIS PHARMACEUTICALS CORP. | M | Y | 20041231 | MD |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4542786 | 1005547041 | SS | ASPIRIN | 1 | ORAL | UNK, UNK | |||||
| 4542786 | 1005547042 | PS | DIOVAN | 1 | ORAL | 80 MG, QD |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4542786 | 1005547042 | HYPERTENSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4542786 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4542786 | DERMATITIS ATOPIC |
| 4542786 | SKIN LESION |
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 |
|---|---|---|---|---|---|
| 4542786 | 1005547042 | 20030818 | 20030922 | 51840 | MIN |