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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4746873 | 5734913 | F | 4746873-4 | 20031001 | 20050131 | 20050817 | EXP | HQWYE031702FEB05 | AMGEN | F | Y | 20050817 | SWEDEN |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
4746873 | 1006328802 | PS | ENBREL | 1 | UNKNOWN | NOT PROVIDED | |||||
4746873 | 1006328803 | SS | INFLIXIMAB | 2 | |||||||
4746873 | 1006328804 | C | METHOTREXATE | 1 | |||||||
4746873 | 1006328805 | C | PREDNISONE | 1 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
4746873 | 1006328802 | RHEUMATOID ARTHRITIS |
Outcome of event
Event ID | OUTC COD |
---|---|
4746873 | OT |
Reactions reported
Event ID | PT |
---|---|
4746873 | BONE TUBERCULOSIS |
4746873 | TUBERCULOSIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |