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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6255541 | 7047695 | I | 6255541-1 | 20090621 | 20090630 | EXP | 8043639 | UCB, INC. | 35 | YR | M | N | 104 | KG | 20090626 | PH | CANADA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6255541 | 1011834562 | PS | CDP870 | 2 | SUBCUTANEOUS | 400 MG SC | D | ||||
| 6255541 | 1011872717 | C | CALCIUM | 2 | |||||||
| 6255541 | 1011872718 | C | VITAMIN D | 1 | |||||||
| 6255541 | 1011872719 | C | TYLENOL | 1 | |||||||
| 6255541 | 1011872720 | C | CIPROFLOXACIN | 2 | |||||||
| 6255541 | 1011872721 | C | FLAGYL | 1 | |||||||
| 6255541 | 1011872722 | C | NEXIUM | 1 | |||||||
| 6255541 | 1011872723 | C | PREDNISONE | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6255541 | 1011834562 | CROHN'S DISEASE |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6255541 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6255541 | BACTEROIDES INFECTION |
| 6255541 | BLOOD MAGNESIUM DECREASED |
| 6255541 | BLOOD PHOSPHORUS DECREASED |
| 6255541 | BLOOD POTASSIUM DECREASED |
| 6255541 | SEPSIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 6255541 | FGN |
| 6255541 | OTH |
| 6255541 | SDY |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6255541 | 1011834562 | 20081216 | 20090226 |