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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5903731 | 6775569 | I | 5903731-7 | 20080922 | 20080930 | PER | US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2008-BP-14813BP | B.I. PHARMACEUTICALS,INC./RIDGEFIELD | 79 | YR | F | Y | 20080930 | PH |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5903731 | 1010521570 | PS | FLOMAX | 1 | F0800001 | 020579 |
Indications of drugs used
no results found |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
5903731 | DRUG INEFFECTIVE |
5903731 | NOCTURIA |
5903731 | POLLAKIURIA |
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 |
---|---|---|---|---|---|
5903731 | 1010521570 | 19980101 |