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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6856750 | 7536569 | I | 6856750-0 | 20100408 | 20100630 | PER | 1000013112 | FOREST LABORATORIES, INC. | YR | UNK | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6856750 | 1014174923 | PS | BYSTOLIC | 1 | ORAL | 5 MG (5 MG, 1 IN 1 D), ORAL | Y | D | 21742 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6856750 | 1014174923 | HYPERTENSION |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
6856750 | DIZZINESS |
6856750 | FATIGUE |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
6856750 | CR |
6856750 | HP |
Therapies reported
no results found |