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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5079236 | 6110153 | I | 5079236-5 | 20041004 | 20060727 | 20060809 | EXP | 2006094166 | PFIZER INC. | 74 | YR | M | N | 175 | LBS | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5079236 | 1007574775 | PS | BEXTRA | 1 | 10 MG | U | U | 21341 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5079236 | 1007574775 | ARTHRALGIA |
| 5079236 | 1007574775 | MUSCULOSKELETAL PAIN |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5079236 | HO |
| 5079236 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5079236 | CEREBROVASCULAR ACCIDENT |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 5079236 | CSM |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 5079236 | 1007574775 | 20020925 |