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Celance Safety Reports
Total Celance reports: 2.Celance FDA safety alerts: No.
Reported deaths: 2 Reported hospitalizations: 2.
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Reported Celance Side Effects: post procedural sepsis, dyspnoea, aortic stenosis, subileus, right ventricular failure, pulmonary hypertension, pulmonary fibrosis, interstitial lung disease, hyponatraemia, blood lactate dehydrogenase increased.
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Celance Side Effects Report #5273409-4
Consumer or non-health professional from FRANCE reported CELANCE problem on Mar 09, 2007. Male patient, 83 years of age, was diagnosed with parkinson's disease and was treated with CELANCE. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, hyponatraemia, interstitial lung disease, pulmonary fibrosis, pulmonary hypertension, right ventricular failure, subileus. CELANCE dosage: 2 MG; QD; PO. During the same period patient was treated with CARBIDOPA, ENTACAPONE, LEVODOPA, PLAVIX, IKOREL. Patient was hospitalized. Patient died on 02/20/2007.
Celance Side Effects Report #5363489-X
CELANCE problem was reported by a Physician from FRANCE on June 01, 2007. Male patient, 70 years of age, was diagnosed with parkinson's disease and was treated with CELANCE. After drug was administered, patient experienced the following problems/side effects: aortic stenosis, dyspnoea, post procedural sepsis. CELANCE dosage: 5 MG; QD; PO. Patient was hospitalized. Patient died on 01/01/2005.