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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127034561 | 12703456 | 1 | I | 20071021 | 20071025 | 20160831 | 20160831 | EXP | US-PFIZER INC-2007089803 | PFIZER | 69.00 | YR | M | Y | 103.00000 | KG | 20160831 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127034561 | 12703456 | 1 | PS | IBUPROFEN. | IBUPROFEN | 1 | Oral | UNK | Y | 18989 | TABLET | ||||||||
| 127034561 | 12703456 | 2 | SS | IBUPROFEN. | IBUPROFEN | 1 | Y | 18989 | TABLET | ||||||||||
| 127034561 | 12703456 | 3 | C | NEXIUM | ESOMEPRAZOLE MAGNESIUM | 1 | Oral | UNK | 0 | ||||||||||
| 127034561 | 12703456 | 4 | C | PREDNISONE. | PREDNISONE | 1 | Oral | UNK | 0 | ||||||||||
| 127034561 | 12703456 | 5 | C | HYDROXYZINE | HYDROXYZINEHYDROXYZINE HYDROCHLORIDE | 1 | Oral | UNK | 0 | ||||||||||
| 127034561 | 12703456 | 6 | C | IBUPROFEN. | IBUPROFEN | 1 | Oral | UNK | 0 | TABLET | |||||||||
| 127034561 | 12703456 | 7 | C | IBUPROFEN. | IBUPROFEN | 1 | Oral | 800 MG, DAILY | 0 | 800 | MG | TABLET | |||||||
| 127034561 | 12703456 | 8 | C | LOTREL | AMLODIPINE BESYLATEBENAZEPRIL HYDROCHLORIDE | 1 | Oral | 1 TABLET, DAILY | 56 | DF | 0 | 1 | DF | TABLET | |||||
| 127034561 | 12703456 | 9 | C | LOTREL | AMLODIPINE BESYLATEBENAZEPRIL HYDROCHLORIDE | 1 | Oral | 1 TABLET TWICE DAILY | 56 | DF | 0 | 1 | DF | TABLET | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127034561 | 12703456 | 1 | Rheumatoid arthritis |
| 127034561 | 12703456 | 2 | Osteoarthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127034561 | 12703456 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127034561 | 12703456 | Cardiac failure congestive | |
| 127034561 | 12703456 | 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 |
|---|---|---|---|---|---|---|
| 127034561 | 12703456 | 1 | 20070924 | 20071020 | 0 | |
| 127034561 | 12703456 | 3 | 20070924 | 20071020 | 0 | |
| 127034561 | 12703456 | 4 | 20070914 | 0 | ||
| 127034561 | 12703456 | 5 | 20070910 | 0 | ||
| 127034561 | 12703456 | 6 | 20040302 | 20070923 | 0 | |
| 127034561 | 12703456 | 7 | 20071021 | 0 | ||
| 127034561 | 12703456 | 8 | 20070907 | 20070923 | 0 | |
| 127034561 | 12703456 | 9 | 20070924 | 20071022 | 0 |