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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5201667 | 6175895 | F | 5201667-0 | 20061031 | 20061114 | 20070108 | EXP | BR-BOEHRINGER INGELHEIM GMBH, GERMANY-2006-UK-04620UK | BOEHRINGER INGELHEIM PHARMACEUTICALS, INC. | M | Y | 122 | KG | 20070108 | 20061106 | BRAZIL |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5201667 | 1008021008 | PS | MICARDIS | 1 | ORAL | ||||||
| 5201667 | 1008021009 | SS | AGGRENOX | 1 | ORAL | ||||||
| 5201667 | 1008021010 | SS | CLOPIDOGREL | 1 | ORAL |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5201667 | 1008021008 | CEREBROVASCULAR ACCIDENT PROPHYLAXIS |
| 5201667 | 1008021009 | CEREBROVASCULAR ACCIDENT PROPHYLAXIS |
| 5201667 | 1008021010 | CEREBROVASCULAR ACCIDENT PROPHYLAXIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5201667 | DE |
| 5201667 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5201667 | CARDIAC ARREST |
| 5201667 | RENAL FAILURE |
| 5201667 | VENTRICULAR FIBRILLATION |
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 |
|---|---|---|---|---|---|
| 5201667 | 1008021008 | 20060512 | |||
| 5201667 | 1008021009 | 20060512 | |||
| 5201667 | 1008021010 | 20060512 |