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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4430568 | 4196922 | I | 4430568-0 | 20040101 | 20040806 | 20040818 | EXP | K200401184 | KING PHARMACEUTICALS, INC. | F | N | 20040817 | OT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4430568 | 1005132460 | PS | ALTACE | 1 | ORAL | 1.25 MG, QD, ORAL | D | D | 19901 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4430568 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4430568 | CHEST PAIN |
| 4430568 | DYSPNOEA |
| 4430568 | ELECTROCARDIOGRAM ABNORMAL |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4430568 | FGN |
| 4430568 | HP |
| 4430568 | OTH |
Therapies reported
| no results found |