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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6856742 | 7536505 | I | 6856742-1 | 20100408 | 20100630 | PER | 1000013109 | FOREST LABORATORIES, INC. | 30 | YR | M | N | 20100610 | MD | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6856742 | 1014174900 | PS | BYSTOLIC | 1 | ORAL | 5 MG (5 MG, 1 IN 1 D), ORAL | Y | D | 21742 | ||
| 6856742 | 1014390453 | C | ZESTRIL | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6856742 | 1014174900 | HYPERTENSION |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 6856742 | DIZZINESS |
| 6856742 | FATIGUE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 6856742 | CR |
| 6856742 | HP |
Therapies reported
| no results found |