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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 105845895 | 10584589 | 5 | F | 201512 | 20160718 | 20141114 | 20160722 | EXP | US-PFIZER INC-2014311353 | PFIZER | 87.00 | YR | F | Y | 53.00000 | KG | 20160722 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 105845895 | 10584589 | 1 | PS | CELEBREX | CELECOXIB | 1 | Oral | 200 MG, 2X/DAY | CI40333 | 20998 | 200 | MG | CAPSULE, HARD | BID | |||||
| 105845895 | 10584589 | 2 | SS | CELEBREX | CELECOXIB | 1 | 20998 | CAPSULE, HARD | |||||||||||
| 105845895 | 10584589 | 3 | SS | CELEBREX | CELECOXIB | 1 | 20998 | CAPSULE, HARD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 105845895 | 10584589 | 1 | Rheumatoid arthritis |
| 105845895 | 10584589 | 2 | Pain |
| 105845895 | 10584589 | 3 | Inflammation |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 105845895 | 10584589 | OT |
| 105845895 | 10584589 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 105845895 | 10584589 | Condition aggravated | |
| 105845895 | 10584589 | Drug dose omission | |
| 105845895 | 10584589 | Fatigue | |
| 105845895 | 10584589 | Pneumonia | |
| 105845895 | 10584589 | Pneumothorax | |
| 105845895 | 10584589 | Tendon disorder |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |