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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4517271 | 5688668 | I | 4517271-3 | 19800101 | 20040728 | 20041001 | PER | PHEH2004US08176 | NOVARTIS | 56 | YR | M | N | 20040820 | CN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4517271 | 1005453198 | PS | LOPRESSOR | 1 | U | U | 17963 | ||||
| 4517271 | 1005457850 | SS | BETA BLOCKING AGENTS(NO INGREDIENTS/SUBSTANCES) | 2 | U | U |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4517271 | 1005453198 | HYPERTENSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4517271 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 4517271 | DEPRESSION |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4517271 | CSM |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4517271 | 1005453198 | 19800101 |