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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6768337 | 7418844 | F | 6768337-9 | 20100529 | 20100604 | 20100614 | EXP | ES-BRISTOL-MYERS SQUIBB COMPANY-15129695 | BRISTOL-MYERS SQUIBB COMPANY | 64 | YR | M | Y | 20100614 | MD | 20100601 | SPAIN |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6768337 | 1013860747 | PS | ORENCIA | 1 | |||||||
6768337 | 1013860748 | SS | VALTREX | 1 | |||||||
6768337 | 1013860749 | SS | DACORTIN | 2 | |||||||
6768337 | 1013860750 | SS | ITRACONAZOLE | 1 | |||||||
6768337 | 1013860751 | SS | SEPTRIN | 2 | |||||||
6768337 | 1013860752 | C | HUMIRA | 1 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6768337 | 1013860747 | RHEUMATOID ARTHRITIS |
Outcome of event
Event ID | OUTC COD |
---|---|
6768337 | DE |
6768337 | HO |
6768337 | OT |
Reactions reported
Event ID | PT |
---|---|
6768337 | ANAEMIA |
6768337 | DYSPNOEA |
6768337 | PULMONARY SEPSIS |
6768337 | PYREXIA |
6768337 | RENAL FAILURE |
6768337 | SHOCK |
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 |
---|---|---|---|---|---|
6768337 | 1013860747 | 20100528 |