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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127971621 | 12797162 | 1 | I | 20160415 | 20160926 | 20160930 | 20160930 | PER | US-PFIZER INC-2016452624 | PFIZER | 67.00 | YR | F | Y | 0.00000 | 20160930 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127971621 | 12797162 | 1 | PS | CELEBREX | CELECOXIB | 1 | Oral | 200 MG, UNK | Y | 20998 | 200 | MG | CAPSULE, HARD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127971621 | 12797162 | 1 | Arthralgia |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127971621 | 12797162 | Drug hypersensitivity | |
127971621 | 12797162 | Muscle contractions involuntary | |
127971621 | 12797162 | Peripheral swelling | |
127971621 | 12797162 | Pyrexia | |
127971621 | 12797162 | Rash |
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 |
---|---|---|---|---|---|---|
127971621 | 12797162 | 1 | 20160314 | 20160506 | 0 |