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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5282302 | 6276629 | I | 5282302-2 | 20070320 | 20070331 | EXP | FI-PFIZER INC-2007023844 | PFIZER INC | 75 | YR | F | Y | 20070330 | MD | FINLAND |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5282302 | 1008316915 | PS | DETRUSITOL SR | 2 | ORAL | 21228 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
5282302 | OT |
Reactions reported
Event ID | PT |
---|---|
5282302 | MUSCULAR WEAKNESS |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |