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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123487796 | 12348779 | 6 | F | 20160810 | 20160509 | 20160816 | PER | US-PFIZER INC-2016049585 | PFIZER | 74.00 | YR | F | Y | 0.00000 | 20160816 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123487796 | 12348779 | 1 | PS | CELEBREX | CELECOXIB | 1 | Oral | 100 MG, (TAKE 1 CAPSULE TWICE A DAY, AS NEEDED) | 20998 | 100 | MG | CAPSULE, HARD | BID | ||||||
| 123487796 | 12348779 | 2 | SS | CELEBREX | CELECOXIB | 1 | UNK UNK, 1X/DAY | 20998 | CAPSULE, HARD | QD | |||||||||
| 123487796 | 12348779 | 3 | SS | CELEBREX | CELECOXIB | 1 | Oral | 100 MG, AS NEEDED(TWICE A DAY) | 20998 | 100 | MG | CAPSULE, HARD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 123487796 | 12348779 | 1 | Rheumatoid arthritis |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123487796 | 12348779 | Arthritis | |
| 123487796 | 12348779 | Blood potassium decreased | |
| 123487796 | 12348779 | Drug ineffective | |
| 123487796 | 12348779 | Intentional product misuse | |
| 123487796 | 12348779 | Peripheral swelling | |
| 123487796 | 12348779 | Tooth extraction |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |