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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126139981 | 12613998 | 1 | I | 20160729 | 20160802 | 20160802 | PER | US-PFIZER INC-2016368665 | PFIZER | 7.00 | DEC | M | Y | 0.00000 | 20160802 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126139981 | 12613998 | 1 | PS | CELEBREX | CELECOXIB | 1 | Oral | 200 MG, ONE CAPSULE BY MOUTH DAILY | 20998 | 200 | MG | CAPSULE, HARD | |||||||
| 126139981 | 12613998 | 2 | C | DULOXETINE. | DULOXETINE | 1 | UNK | 0 | |||||||||||
| 126139981 | 12613998 | 3 | C | NEXIUM | ESOMEPRAZOLE MAGNESIUM | 1 | UNK | 0 | |||||||||||
| 126139981 | 12613998 | 4 | C | TAMSULOSIN | TAMSULOSIN | 1 | UNK | 0 |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126139981 | 12613998 | Drug hypersensitivity | |
| 126139981 | 12613998 | Fatigue | |
| 126139981 | 12613998 | Reaction to drug excipients |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |