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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6382366 | 7113501 | F | 6382366-9 | 20090401 | 20090921 | 20090930 | PER | US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2009-BP-10420BP | B.I. PHARMACEUTICALS,INC./RIDGEFIELD | 56 | F | Y | 20090930 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6382366 | 1012353992 | PS | SPIRIVA | 1 | 18 MCG | NOT REPORTED | 021395 | ||||
| 6382366 | 1012353993 | SS | COMBIVENT | 1 | NOT REPORTED | 020291 | |||||
| 6382366 | 1012353994 | SS | QVAR 40 | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6382366 | 1012353992 | CHRONIC OBSTRUCTIVE PULMONARY DISEASE |
| 6382366 | 1012353993 | DYSPNOEA |
| 6382366 | 1012353994 | DYSPNOEA |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 6382366 | DRY MOUTH |
| 6382366 | ORAL DISCOMFORT |
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 |
|---|---|---|---|---|---|
| 6382366 | 1012353992 | 20090401 |