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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125317593 | 12531759 | 3 | F | 20160604 | 20160913 | 20160706 | 20160919 | PER | US-PFIZER INC-2016291851 | PFIZER | 58.00 | YR | F | Y | 65.77000 | KG | 20160919 | MD | US | SG |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125317593 | 12531759 | 1 | PS | CELEBREX | CELECOXIB | 1 | 200 MG, DAILY | C140332 | 20998 | 200 | MG | CAPSULE, HARD | |||||||
125317593 | 12531759 | 2 | SS | CELEBREX | CELECOXIB | 1 | 200 MG, DAILY | C140333 | 20998 | 200 | MG | CAPSULE, HARD | |||||||
125317593 | 12531759 | 3 | SS | PERCOCET | ACETAMINOPHENOXYCODONE HYDROCHLORIDE | 1 | 60 MG, DAILY (10MG 6/DAY) | 0 | 60 | MG |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125317593 | 12531759 | 1 | Back pain |
125317593 | 12531759 | 3 | Back pain |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125317593 | 12531759 | Back pain | |
125317593 | 12531759 | Condition aggravated |
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 |
---|---|---|---|---|---|---|
125317593 | 12531759 | 1 | 2012 | 0 | ||
125317593 | 12531759 | 2 | 201607 | 0 | ||
125317593 | 12531759 | 3 | 2014 | 0 |