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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6142810 | 7202769 | I | 6142810-9 | 20071203 | 20090402 | DIR | 65 | YR | M | N | 86.7 | KG | PH | N | Y | UNITED STATES |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6142810 | 1011376399 | PS | ABATACEPT | 2 | SUBCUTANEOUS | 50 MG QWEEK SQ | Y |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6142810 | 1011376399 | RHEUMATOID ARTHRITIS |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
6142810 | CHRONIC OBSTRUCTIVE PULMONARY DISEASE |
6142810 | CONDITION AGGRAVATED |
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 |
---|---|---|---|---|---|
6142810 | 1011376399 | 20070813 | 20071203 |