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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127000101 | 12700010 | 1 | I | 20140108 | 20140204 | 20160830 | 20160830 | EXP | US-PFIZER INC-2014032272 | PFIZER | 58.00 | YR | M | Y | 102.00000 | KG | 20160830 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127000101 | 12700010 | 1 | PS | IBUPROFEN. | IBUPROFEN | 1 | Oral | UNK | Y | 18989 | TABLET | ||||||||
| 127000101 | 12700010 | 2 | SS | IBUPROFEN. | IBUPROFEN | 1 | Y | 18989 | TABLET | ||||||||||
| 127000101 | 12700010 | 3 | C | NEXIUM | ESOMEPRAZOLE MAGNESIUM | 1 | Oral | 40 MG, 1X/DAY | 16600 | MG | 0 | 40 | MG | QD | |||||
| 127000101 | 12700010 | 4 | C | ASPIRIN. | ASPIRIN | 1 | Oral | 81 MG, 1X/DAY | 0 | 81 | MG | QD | |||||||
| 127000101 | 12700010 | 5 | C | ALLOPURINOL. | ALLOPURINOL | 1 | Oral | 300 MG, 1X/DAY | 0 | 300 | MG | QD | |||||||
| 127000101 | 12700010 | 6 | C | MULTIVITAMINS | VITAMINS | 1 | Oral | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127000101 | 12700010 | 1 | Rheumatoid arthritis |
| 127000101 | 12700010 | 2 | Osteoarthritis |
| 127000101 | 12700010 | 3 | Prophylaxis |
| 127000101 | 12700010 | 4 | Cardiovascular event prophylaxis |
| 127000101 | 12700010 | 5 | Gout |
| 127000101 | 12700010 | 6 | Vitamin supplementation |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127000101 | 12700010 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127000101 | 12700010 | Condition aggravated | |
| 127000101 | 12700010 | Deep vein thrombosis |
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 |
|---|---|---|---|---|---|---|
| 127000101 | 12700010 | 1 | 20121120 | 20140107 | 0 | |
| 127000101 | 12700010 | 3 | 20121120 | 20140108 | 0 | |
| 127000101 | 12700010 | 4 | 2008 | 0 | ||
| 127000101 | 12700010 | 5 | 2012 | 0 | ||
| 127000101 | 12700010 | 6 | 2006 | 0 |