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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6527771 | 7247320 | F | 1 | 6527771-2 | 20090428 | 20091102 | 20091231 | EXP | 003528 | UCB, INC. | 9 | F | N | 29 | KG | 20091230 | OT | GERMANY |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6527771 | 1012904007 | PS | XUSAL (XUSAL) | 2 | ORAL | (10 MG TID ORAL) | D | D | 22064 | ||
| 6527771 | 1012951708 | C | INSULIN HUMAN | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6527771 | 1012904007 | URTICARIA CHRONIC |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6527771 | HO |
| 6527771 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6527771 | BLOOD PRESSURE SYSTOLIC DECREASED |
| 6527771 | EPILEPSY |
| 6527771 | GENERAL PHYSICAL HEALTH DETERIORATION |
| 6527771 | HYPOGLYCAEMIA |
| 6527771 | LISTLESS |
| 6527771 | LOSS OF CONSCIOUSNESS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 6527771 | FGN |
| 6527771 | HP |
| 6527771 | OTH |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6527771 | 1012904007 | 20090401 |