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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5215222 | 6238683 | I | 5215222-X | 20060101 | 20060421 | 20061120 | PER | HQWYE970025APR06 | WYETH CONSUMER HEALTHCARE | N | 20061114 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5215222 | 1008066404 | PS | ADVIL COLD AND SINUS | 1 | ORAL | 1 TABLET AS NEEDED, ORAL | D | D | 19771 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5215222 | 1008066404 | SINUS DISORDER |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5215222 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5215222 | FEELING JITTERY |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 5215222 | CSM |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 5215222 | 1008066404 | 20061001 |