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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5120032 | 6114510 | F | 2 | 5120032-8 | 20060626 | 20060920 | 20060929 | EXP | 2006090166 | PFIZER INC | 64 | YR | F | N | 154 | LBS | 20060928 | PH | IRELAND |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5120032 | 1007726846 | PS | CARDURA | 1 | ORAL | 8 MG (4 MG, 2 IN 1 D), ORAL | D | D | 61(7)0027830 | 20070401 | 21269 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5120032 | 1007726846 | HYPERTENSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5120032 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5120032 | DIARRHOEA |
| 5120032 | HEADACHE |
| 5120032 | NAUSEA |
| 5120032 | PHARMACEUTICAL PRODUCT COMPLAINT |
| 5120032 | VISION BLURRED |
| 5120032 | VISUAL DISTURBANCE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 5120032 | CSM |
| 5120032 | FGN |
| 5120032 | HP |
Therapies reported
| no results found |