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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4392607 | 4167524 | F | 1 | 4392607-5 | 20040618 | 20040702 | EXP | 2004-BP-03764RP | B.I. (PHIL) INC. | 84 | YR | F | N | 20040629 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4392607 | 1004995841 | PS | MICARDIS HCT | 1 | ORAL | 80 MG, 1 TAB OD, PO | D | 21162 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4392607 | 1004995841 | HYPERTENSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4392607 | DE |
Reactions reported
| Event ID | PT |
|---|---|
| 4392607 | BLOOD PRESSURE INCREASED |
| 4392607 | BRAIN HERNIATION |
| 4392607 | CEREBRAL INFARCTION |
| 4392607 | CEREBROVASCULAR ACCIDENT |
| 4392607 | PNEUMONIA |
| 4392607 | SEPSIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4392607 | FGN |
| 4392607 | HP |
| 4392607 | OTH |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4392607 | 1004995841 | 20030205 |