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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5079238 | 6110157 | I | 5079238-9 | 20030503 | 20060727 | 20060809 | EXP | 2006094095 | PFIZER INC. | 52 | YR | F | N | 20060808 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5079238 | 1007574783 | PS | CELEBREX | 1 | 400 MG (200 MG, 2 IN 1 D) | D | D | 20998 | |||
| 5079238 | 1007591055 | SS | BEXTRA | 1 | SEE IMAGE | D | D |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5079238 | 1007574783 | ARTHRITIS |
| 5079238 | 1007591055 | ARTHRITIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5079238 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5079238 | ANXIETY |
| 5079238 | DEEP VEIN THROMBOSIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 5079238 | CSM |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 5079238 | 1007574783 | 20020311 | 20020717 | ||
| 5079238 | 1007591055 | 20021105 | 20021128 | ||
| 5079238 | 1007591055 | 20021129 | 20030423 |