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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122783553 | 12278355 | 3 | F | 20160705 | 20160418 | 20160711 | EXP | US-PFIZER INC-2016210814 | PFIZER | 76.00 | YR | F | Y | 0.00000 | 20160711 | MD | US | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122783553 | 12278355 | 1 | PS | CELEBREX | CELECOXIB | 1 | 200 MG, 1X/DAY | N | 20998 | 200 | MG | CAPSULE, HARD | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 122783553 | 12278355 | 1 | Pain |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 122783553 | 12278355 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 122783553 | 12278355 | Asthenia | |
| 122783553 | 12278355 | Fall | |
| 122783553 | 12278355 | Gait disturbance | |
| 122783553 | 12278355 | Insomnia | |
| 122783553 | 12278355 | Lower limb fracture | |
| 122783553 | 12278355 | Renal disorder | |
| 122783553 | 12278355 | Upper limb fracture |
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 |
|---|---|---|---|---|---|---|
| 122783553 | 12278355 | 1 | 2016 | 0 |