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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 107217405 | 10721740 | 5 | F | 2002 | 20160802 | 20150119 | 20160808 | EXP | US-PFIZER INC-2015019218 | PFIZER | 54.00 | YR | M | Y | 99.79000 | KG | 20160808 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 107217405 | 10721740 | 1 | PS | CELEBREX | CELECOXIB | 1 | 200 MG, UNK | U | 20998 | 200 | MG | CAPSULE, HARD | |||||||
| 107217405 | 10721740 | 2 | SS | CELEBREX | CELECOXIB | 1 | U | 20998 | CAPSULE, HARD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 107217405 | 10721740 | 1 | Joint swelling |
| 107217405 | 10721740 | 2 | Inflammation |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 107217405 | 10721740 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 107217405 | 10721740 | Arthropathy | |
| 107217405 | 10721740 | Asthma | |
| 107217405 | 10721740 | Condition aggravated | |
| 107217405 | 10721740 | Malaise |
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 |
|---|---|---|---|---|---|---|
| 107217405 | 10721740 | 1 | 2002 | 2015 | 0 |