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Soprol Safety Reports submitted to FDA

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Total Soprol reports: 2.
Soprol FDA safety alerts: No.
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Reported Soprol Side Effects: ventricular tachycardia, syncope, respiratory failure, pulmonary fibrosis, pulmonary eosinophilia, interstitial lung disease.
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Soprol Side Effects Report #5347966-3
Health Professional from FRANCE reported SOPROL problem on May 31, 2007. Male patient, 66 years of age, weighting 187.4 lb, was diagnosed with nasopharyngitis and was treated with SOPROL. After drug was administered, patient experienced the following problems/side effects: interstitial lung disease, pulmonary eosinophilia, pulmonary fibrosis, respiratory failure. SOPROL dosage: unknown. During the same period patient was treated with PLAVIX, PROPOLIS. Patient recovered.

Soprol Side Effects Report #5372547-5
SOPROL problem was reported by a Consumer or non-health professional from FRANCE on June 12, 2007. Female patient, 31 years of age, was diagnosed with congestive cardiomyopathy and was treated with SOPROL. After drug was administered, patient experienced the following problems/side effects: syncope, ventricular tachycardia. SOPROL dosage: 10 MG (10 MG, 1 IN 1 D), ORAL. During the same period patient was treated with NADOLOL. Patient recovered.


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interstitial lung disease, pulmonary eosinophilia, pulmonary fibrosis, respiratory failure syncope, ventricular tachycardia, was diagnosed with nasopharyngitis and was diagnosed with congestive cardiomyopathy and