Coniel Side Effects
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Coniel Safety Reports reported to FDA
Total Coniel reports: 3.Coniel FDA safety alerts: No.
Reported deaths: 3 Reported hospitalizations: 3.
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Reported Coniel Side Effects: blood urea increased, blood sodium decreased, blood potassium increased, blood culture positive, blood creatinine increased, blood cholesterol increased, blood albumin decreased, asthenia, ascites.
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Coniel Side Effects Report #5115518-6
Physician from JAPAN reported CONIEL problem on May 18, 2006. Female patient, 75 years of age, weighting 127.9 lb, was diagnosed with hypertension, asthma, gastritis, musculoskeletal pain, dysthymic disorder and was treated with CONIEL. After drug was administered, patient experienced the following problems/side effects: ascites, asthenia, blood albumin decreased, blood cholesterol increased, blood creatinine increased, blood culture positive, blood potassium increased, blood sodium decreased, blood urea increased. CONIEL dosage: 8 MG, UNK. During the same period patient was treated with PREDNISOLONE, FAMOTIDINE, HYPEN, TRYPTANOL, LEVOTOMIN, MEILAX, DIOVAN. Patient was hospitalized. Patient died on 07/03/2006.
Coniel Side Effects Report #5133418-2
CONIEL problem was reported by a Physician from JAPAN on May 18, 2006. Female patient, 75 years of age, weighting 127.9 lb, was diagnosed with hypertension, asthma, gastritis, musculoskeletal pain, dysthymic disorder and was treated with CONIEL. After drug was administered, patient experienced the following problems/side effects: ascites, asthenia, blood albumin decreased, blood cholesterol increased, blood creatinine increased, blood culture positive, blood potassium increased, blood sodium decreased, blood urea increased. CONIEL dosage: 8 MG, UNK. During the same period patient was treated with PREDNISOLONE, FAMOTIDINE, HYPEN, TRYPTANOL, LEVOTOMIN, MEILAX, DIOVAN. Patient was hospitalized. Patient died on 07/03/2006.
Coniel Side Effects Report #5153789-0
Physician from JAPAN reported CONIEL problem on May 18, 2006. Female patient, 75 years of age, weighting 127.9 lb, was diagnosed with hypertension, asthma, gastritis, musculoskeletal pain, dysthymic disorder and was treated with CONIEL. After drug was administered, patient experienced the following problems/side effects: ascites, asthenia, blood albumin decreased, blood cholesterol increased, blood creatinine increased, blood culture positive, blood potassium increased, blood sodium decreased, blood urea increased. CONIEL dosage: 8 MG, UNK. During the same period patient was treated with PREDNISOLONE, FAMOTIDINE, HYPEN, TRYPTANOL, LEVOTOMIN, MEILAX, DIOVAN. Patient was hospitalized. Patient died on 07/03/2006.