Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126329291 | 12632929 | 1 | I | 20160806 | 0 | 20160808 | 20160808 | DIR | 43.00 | YR | F | N | 230.00000 | LBS | 20160806 | Y | US |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126329291 | 12632929 | 1 | PS | PROAIR HFA | ALBUTEROL SULFATE | 1 | Respiratory (inhalation) | 200 PUFF(S) | Y | Y | DAC28A | 20090831 | 0 | PRN | |||||
| 126329291 | 12632929 | 3 | C | ALBUTEROL. | ALBUTEROL | 1 | 0 | ||||||||||||
| 126329291 | 12632929 | 5 | C | TYLENOL | ACETAMINOPHEN | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126329291 | 12632929 | 1 | Asthma |
| 126329291 | 12632929 | 1 | Multiple allergies |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126329291 | 12632929 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126329291 | 12632929 | Asthma | |
| 126329291 | 12632929 | Drug ineffective |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 126329291 | 12632929 | 1 | 20160802 | 20160806 | 0 |