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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5287758 | 6448492 | I | 5287758-7 | 20070316 | 20070402 | DIR | 35 | YR | F | N | 180 | LBS | 20070331 | CN | N | N | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5287758 | 1008334057 | PS | PROAIR HFA | 1 | RESPIRATORY (INHALATION) | AS NEEDED VERY OFTEN INHAL | D | D | ADN04A | 20080401 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5287758 | 1008334057 | ASTHMA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5287758 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5287758 | DRUG EFFECT DECREASED |
| 5287758 | DYSPNOEA |
| 5287758 | PHARMACEUTICAL PRODUCT COMPLAINT |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |