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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127070641 | 12707064 | 1 | I | 20130725 | 20130821 | 20160901 | 20160901 | EXP | US-PFIZER INC-2013241581 | PFIZER | 48.00 | YR | M | Y | 111.80000 | KG | 20160901 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127070641 | 12707064 | 1 | PS | IBUPROFEN. | IBUPROFEN | 1 | Oral | UNK | Y | 18989 | TABLET | ||||||||
127070641 | 12707064 | 2 | SS | IBUPROFEN. | IBUPROFEN | 1 | Y | 18989 | TABLET | ||||||||||
127070641 | 12707064 | 3 | C | PRILOSEC | OMEPRAZOLE MAGNESIUM | 1 | Oral | 1 TAB, QD | 0 | 1 | DF | TABLET | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127070641 | 12707064 | 1 | Osteoarthritis |
127070641 | 12707064 | 2 | Rheumatoid arthritis |
127070641 | 12707064 | 3 | Prophylaxis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127070641 | 12707064 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127070641 | 12707064 | Chest pain |
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 |
---|---|---|---|---|---|---|
127070641 | 12707064 | 1 | 20120821 | 20130819 | 0 | |
127070641 | 12707064 | 3 | 2000 | 0 |