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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5282272 | 6276590 | I | 5282272-7 | 20070320 | 20070331 | EXP | US-PFIZER INC-2007023215 | PFIZER INC | F | Y | 20070330 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5282272 | 1008316791 | PS | NORVASC | 1 | 019787 | ||||||
| 5282272 | 1008316792 | SS | LISINOPRIL | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5282272 | 1008316791 | HYPERTENSION |
| 5282272 | 1008316792 | HYPERTENSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5282272 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5282272 | LABORATORY TEST ABNORMAL |
| 5282272 | RENAL DISORDER |
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 |
|---|---|---|---|---|---|
| 5282272 | 1008316792 | 20050101 | 20060801 |