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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126833992 | 12683399 | 2 | F | 201608 | 20160912 | 20160825 | 20160915 | PER | US-PFIZER INC-2016398456 | PFIZER | 52.00 | YR | F | Y | 0.00000 | 20160915 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126833992 | 12683399 | 1 | PS | CELEBREX | CELECOXIB | 1 | 50 MG, 2X/DAY | 20998 | 50 | MG | CAPSULE, HARD | BID | |||||||
126833992 | 12683399 | 2 | C | PRILOSEC | OMEPRAZOLE MAGNESIUM | 1 | UNK | 0 | |||||||||||
126833992 | 12683399 | 3 | C | ULTRAM | TRAMADOL HYDROCHLORIDE | 1 | 50 MG, UNK (1-2/ DAY) | 0 | 50 | MG |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126833992 | 12683399 | 1 | Fibromyalgia |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126833992 | 12683399 | Drug ineffective | |
126833992 | 12683399 | Drug intolerance | |
126833992 | 12683399 | Feeling abnormal | |
126833992 | 12683399 | Nervousness | |
126833992 | 12683399 | Product use issue | |
126833992 | 12683399 | Somnolence |
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 |
---|---|---|---|---|---|---|
126833992 | 12683399 | 1 | 201608 | 201608 | 0 |