Person who experienced the adverse event (patient)
Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4542782 | 4153562 | F | 4542782-4 | 20040204 | 20040531 | 20041231 | EXP | 200411891JP | AVENTIS PHARMACEUTICALS, INC. | 38 | YR | F | Y | 58 | KG | 20041231 | MD |
Drug(s) used by person
Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
---|---|---|---|---|---|---|---|---|---|---|---|
4542782 | 1005546997 | PS | ARAVA | 1 | ORAL | ||||||
4542782 | 1005546998 | C | RIMATIL | 2 | ORAL | ||||||
4542782 | 1005546999 | C | RHEUMATREX | 1 | ORAL | ||||||
4542782 | 1005547000 | C | PREDNISOLONE | 1 | ORAL | ||||||
4542782 | 1005547001 | C | VOLTAREN SUPPOSITORIEN | 2 | RECTAL |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
4542782 | 1005546997 | RHEUMATOID ARTHRITIS |
Outcome of event
Event ID | OUTC COD |
---|---|
4542782 | HO |
4542782 | OT |
Reactions reported
Event ID | PT |
---|---|
4542782 | ALANINE AMINOTRANSFERASE INCREASED |
4542782 | ASPARTATE AMINOTRANSFERASE INCREASED |
4542782 | BLOOD LACTATE DEHYDROGENASE INCREASED |
4542782 | DIALYSIS |
4542782 | DIARRHOEA |
4542782 | MONOCYTE PERCENTAGE INCREASED |
4542782 | NAUSEA |
4542782 | RED BLOOD CELL COUNT DECREASED |
4542782 | RENAL FAILURE ACUTE |
4542782 | VOMITING |
4542782 | WHITE BLOOD CELL COUNT INCREASED |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
4542782 | 1005546997 | 20040122 | 20040706 | ||
4542782 | 1005546999 | 20040317 | |||
4542782 | 1005547000 | 20040624 | 20040623 |