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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6663298 | 7346658 | I | 6663298-5 | 20091103 | 20100331 | DIR | 53 | YR | M | N | 20100107 | PH | N | Y | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6663298 | 1013427708 | PS | LISINOPRIL | 1 | ORAL | 10 MG EVERY DAY PO | Y |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6663298 | 1013427708 | HYPERTENSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6663298 | HO |
| 6663298 | RI |
Reactions reported
| Event ID | PT |
|---|---|
| 6663298 | ANGIOEDEMA |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6663298 | 1013427708 | 20091102 | 20091103 |