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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6856741 | 7536498 | I | 6856741-X | 20100328 | 20100407 | 20100630 | PER | 1000013045 | FOREST LABORATORIES, INC. | 67 | YR | F | N | 20100610 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6856741 | 1014174899 | PS | BYSTOLIC | 1 | ORAL | ( 1 IN 1 D), ORAL | D | D | 21742 | ||
6856741 | 1014390436 | C | METFORMIN | 2 | |||||||
6856741 | 1014390437 | C | ASPIRIN | 1 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6856741 | 1014174899 | HYPERTENSION |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
6856741 | RASH |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
6856741 | CSM |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
6856741 | 1014174899 | 20100326 |