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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5903730 | 6775568 | I | 5903730-5 | 20080923 | 20080923 | 20080930 | PER | US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2008-BP-14823BP | B.I. PHARMACEUTICALS,INC./RIDGEFIELD | F | Y | 20080930 | CN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5903730 | 1010521569 | PS | SPIRIVA | 1 | ORAL | NOT REPORTED,NOT REPORTED | 021395 |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 5903730 | INCORRECT ROUTE OF DRUG ADMINISTRATION |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |