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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5282281 | 6276601 | I | 5282281-8 | 20070312 | 20070319 | 20070331 | EXP | JP-PFIZER INC-2007023392 | PFIZER INC | 70 | YR | M | Y | 20070330 | PH | JAPAN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5282281 | 1008316809 | PS | DETRUSITOL SR | 2 | ORAL | DAILY DOSE:2MG | 21228 | ||||
| 5282281 | 1008316810 | C | MUCODYNE | 2 | ORAL | ||||||
| 5282281 | 1008316811 | C | THEOLONG | 2 | ORAL | ||||||
| 5282281 | 1008316812 | C | TAMSULOSIN HCL | 1 | ORAL |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5282281 | 1008316809 | POLLAKIURIA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5282281 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5282281 | HYPERTENSION |
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 |
|---|---|---|---|---|---|
| 5282281 | 1008316809 | 20061225 | 20070312 |