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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4585513 | 5745702 | I | 4585513-4 | 20041231 | DIR | 83 | YR | F | N | 20041231 | N | Y |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
4585513 | 1005699772 | PS | TOPROL-XL | 1 | TABLET | ||||||
4585513 | 1005739224 | SS | TOPAMAX | 1 |
Indications of drugs used
no results found |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
4585513 | BLOOD PRESSURE SYSTOLIC INCREASED |
4585513 | MEDICATION ERROR |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |