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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120658566 | 12065856 | 6 | F | 2015 | 20160722 | 20160211 | 20160728 | PER | US-PFIZER INC-2016077892 | PFIZER | 72.00 | YR | F | Y | 91.00000 | KG | 20160728 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120658566 | 12065856 | 1 | PS | CELEBREX | CELECOXIB | 1 | Oral | 400 MG, 2X/DAY | Y | 20998 | 400 | MG | CAPSULE, HARD | BID | |||||
| 120658566 | 12065856 | 2 | SS | CELEBREX | CELECOXIB | 1 | Oral | 200 MG, 2X/DAY | Y | 20998 | 200 | MG | CAPSULE, HARD | BID | |||||
| 120658566 | 12065856 | 3 | SS | CELEBREX | CELECOXIB | 1 | Oral | UNK, 4X/DAY | Y | 20998 | CAPSULE, HARD | QID | |||||||
| 120658566 | 12065856 | 4 | SS | CELEBREX | CELECOXIB | 1 | 400 MG, DAILY | Y | 20998 | 400 | MG | CAPSULE, HARD | |||||||
| 120658566 | 12065856 | 5 | C | BYSTOLIC | NEBIVOLOL HYDROCHLORIDE | 1 | Oral | 20 MG, 1X/DAY (10MG, 2 TABLETS BY MOUTH DAILY) | 0 | 20 | MG | TABLET | QD | ||||||
| 120658566 | 12065856 | 6 | C | EXFORGE | AMLODIPINE BESYLATEVALSARTAN | 1 | Oral | AMLODIPINE BESILATE/VALSARTAN10-320MG , 1X/DAY | 0 | TABLET | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 120658566 | 12065856 | 1 | Rheumatoid arthritis |
| 120658566 | 12065856 | 5 | Hypertension |
| 120658566 | 12065856 | 6 | Hypertension |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 120658566 | 12065856 | OT |
| 120658566 | 12065856 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 120658566 | 12065856 | Condition aggravated | |
| 120658566 | 12065856 | Hypertension | |
| 120658566 | 12065856 | Rheumatoid arthritis |
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 |
|---|---|---|---|---|---|---|
| 120658566 | 12065856 | 2 | 1994 | 20160205 | 0 | |
| 120658566 | 12065856 | 5 | 1994 | 0 | ||
| 120658566 | 12065856 | 6 | 1994 | 2015 | 0 |