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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7396318 | 7902598 | I | 7396318-3 | 20110331 | DIR | 58 | YR | F | N | 154 | LBS | 20110325 | CN | N | N | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7396318 | 1016179380 | PS | METOPROLOL SUCCINATE EXTENDED RELEASE | 1 | ORAL | 1 TABLET, BY MOUTH 1X DAILY | Y | D |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7396318 | 1016179380 | ATRIAL FIBRILLATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7396318 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 7396318 | UNEVALUABLE EVENT |
| 7396318 | FATIGUE |
| 7396318 | PALPITATIONS |
| 7396318 | CHEST DISCOMFORT |
| 7396318 | CHEST PAIN |
| 7396318 | EXERCISE TOLERANCE DECREASED |
| 7396318 | DIZZINESS |
| 7396318 | PRODUCT QUALITY ISSUE |
| 7396318 | DYSPNOEA EXERTIONAL |
| 7396318 | PRODUCT MEASURED POTENCY ISSUE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |