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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 114680703 | 11468070 | 3 | F | 20160627 | 20150908 | 20160725 | PER | US-PFIZER INC-2015293195 | PFIZER | 64.00 | YR | M | Y | 105.21000 | KG | 20160725 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 114680703 | 11468070 | 1 | PS | CELEBREX | CELECOXIB | 1 | 200 MG, 2X/DAY (ONE IN THE MORNING AND ONE AT NIGHT) | C140309 | 20998 | 200 | MG | CAPSULE, HARD | BID | ||||||
| 114680703 | 11468070 | 2 | SS | LORTAB | ACETAMINOPHENHYDROCODONE BITARTRATE | 1 | 7.5 MG (HALF OF IT AND IT WAS NOT EVERY DAY) | N | 0 | 7.5 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 114680703 | 11468070 | 1 | Arthritis |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 114680703 | 11468070 | Pain | |
| 114680703 | 11468070 | Weight increased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |