CYPHER SIROLIMUS-ELUTING CORONARY STENT Adverse Event — Report (MDR 9616099-2008-00369)
CYPHER SIROLIMUS-ELUTING CORONARY STENT Adverse Event — Report (MDR 9616099-2008-00369) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CYPHER SIROLIMUS-ELUTING CORONARY STENT; Generic name: DRUG-ELUTING STENT (NIQ); Manufacturer: CORDIS DE MEXICO.
| Device | CYPHER SIROLIMUS-ELUTING CORONARY STENT |
|---|---|
| Generic name | DRUG-ELUTING STENT (NIQ) |
| Manufacturer | CORDIS DE MEXICO |
| Report number | 9616099-2008-00369 |
| Product problem | N |
| Date received | 2008-02-15 |
| Report source | Foreign, Health Professional, Company representation |
| Narrative | THE FOLLOWING REPORT WAS RECEIVED FROM THE AFFILIATE: ON 12/2007 AN X-RAY WAS PERFORMED FOR PROGNOSIS OF PANCREATODUODENECTOMY. AFTER THAT, THE PATIENT COMPLAINED OF CHEST DISCOMFORT AND ABNORMAL ELECTROCARDIOGRAM (ECG) WAS OBSERVED. CORONARY ANGIOGRAM (CAG) WAS CONDUCTED AND THROMBUS WAS OBSERVED IN THE 2ND CYPHER AT THE CIRCUMFLEX. THROMBUS WAS NOT OBSERVED IN THE 1ST CYPHER AT THE LAD. TO TREAT |
| Source | openFDA MAUDE (device adverse events) |
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