Mytelase Side Effects
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Recent Mytelase Side Effect Reports
Mytelase Side Effects Report #5404816-4
Physician from JAPAN reported Mytelase side effect on July 27, 2007. Male patient, 76 years of age, weighting 101.4 lb, was diagnosed with myasthenia gravis, hypertension, oral candidiasis, urine output decreased, gastric ulcer, delirium and was treated with Mytelase. After drug was administered, patient experienced the following side effects: bronchopulmonary aspergillosis. Mytelase dosage: unknown. During the same period patient was treated with PROGRAF, ENALAPRIL MALEATE, ARTIST, FLORID, FUROSEMIDE, FAMOTIDINE, RISPERDAL, NEORAL. Patient died on 02/11/2007.
Mytelase Side Effects Report #5422002-9
Mytelase side effect was reported by a Physician from JAPAN on Aug 17, 2007. Male patient, 76 years of age, weighting 101.4 lb, was diagnosed with myasthenia gravis, hypertension, oral candidiasis, urine output decreased, gastric ulcer, delirium and was treated with Mytelase. After drug was administered, patient experienced the following side effects: bronchopulmonary aspergillosis. Mytelase dosage: unknown. During the same period patient was treated with PROGRAF, RENIVACE, ARTIST, FLORID, FUROSEMIDE, FAMOTIDINE, RISPERDAL, NEORAL. Patient died on 02/11/2007.
Physician from JAPAN reported Mytelase side effect on July 27, 2007. Male patient, 76 years of age, weighting 101.4 lb, was diagnosed with myasthenia gravis, hypertension, oral candidiasis, urine output decreased, gastric ulcer, delirium and was treated with Mytelase. After drug was administered, patient experienced the following side effects: bronchopulmonary aspergillosis. Mytelase dosage: unknown. During the same period patient was treated with PROGRAF, ENALAPRIL MALEATE, ARTIST, FLORID, FUROSEMIDE, FAMOTIDINE, RISPERDAL, NEORAL. Patient died on 02/11/2007.
Mytelase Side Effects Report #5422002-9
Mytelase side effect was reported by a Physician from JAPAN on Aug 17, 2007. Male patient, 76 years of age, weighting 101.4 lb, was diagnosed with myasthenia gravis, hypertension, oral candidiasis, urine output decreased, gastric ulcer, delirium and was treated with Mytelase. After drug was administered, patient experienced the following side effects: bronchopulmonary aspergillosis. Mytelase dosage: unknown. During the same period patient was treated with PROGRAF, RENIVACE, ARTIST, FLORID, FUROSEMIDE, FAMOTIDINE, RISPERDAL, NEORAL. Patient died on 02/11/2007.
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Mytelase Adverse Effect Reports (FDA)
Consumer or non-health professional from FRANCE reported Mytelase side effect on Aug 17, 2007. Female patient, 43 years of age, was treated with Mytelase. After drug was administered, patient experienced the following side effects: back pain
, malaise, movement disorder , muscle spasms, pain in extremity, posture abnormal, speech disorder, vertigo. Mytelase dosage: 30 MG. Patient was hospitalized.
Mytelase Side Effects Report #5661862-3
Mytelase side effect was reported by a Health Professional from JAPAN on Feb 29, 2008. Male patient was diagnosed with muscular weakness and was treated with Mytelase. After drug was administered, patient experienced the following side effects: cardio-respiratory arrest. Mytelase dosage: 15 MG.
Mytelase Side Effects Report #5740221-9
Health Professional from JAPAN reported Mytelase side effect on May 05, 2008. Male patient, 67 years of age, was diagnosed with myasthenia gravis and was treated with Mytelase. After drug was administered, patient experienced the following side effects: abdominal pain, pancreatitis. Mytelase dosage: 20 MG. During the same period patient was treated with PYRIDOSTIGMINE BROMIDE, PYRIDOSTIGMINE BROMIDE. Patient was hospitalized.
Mytelase Side Effects Report #5746907-4
Mytelase side effect was reported by a Health Professional from JAPAN on May 13, 2008. Male patient, 67 years of age, was diagnosed with myasthenia gravis and was treated with Mytelase. After drug was administered, patient experienced the following side effects: abdominal pain, pancreatitis. Mytelase dosage: 20 MG. During the same period patient was treated with PYRIDOSTIGMINE BROMIDE, PYRIDOSTIGMINE BROMIDE. Patient was hospitalized.
Mytelase Side Effects Report #5840480-8
Health Professional from JAPAN reported Mytelase side effect on July 30, 2008. Male patient, 55 years of age, was diagnosed with muscular weakness and was treated with Mytelase. After drug was administered, patient experienced the following side effects: brugada syndrome, bundle branch block right, electrocardiogram st segment elevation, loss of consciousness, ventricular extrasystoles, ventricular fibrillation. Mytelase dosage: 20 MG. Patient was hospitalized.
Mytelase Side Effects Report #6030274-5
Mytelase side effect was reported by a Pharmacist from FRANCE on Dec 29, 2008. Female patient, weighting 8.82 lb, was diagnosed with myasthenic syndrome and was treated with Mytelase. After drug was administered, patient experienced the following side effects: cholinergic syndrome, convulsion, diarrhoea, miosis, overdose, vomiting. Mytelase dosage: 2 MG. During the same period patient was treated with PERFALGAN, NEXIUM, PHOCYTAN, UVESTEROL.
Mytelase Side Effects Report #4608968-5
Consumer or non-health professional from reported Mytelase side effect on Jan 21, 2005. Male patient, 56 years of age, was diagnosed with myasthenia gravis and was treated with Mytelase. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, blood lactate dehydrogenase increased, thymectomy. Mytelase dosage: 20MG PO. During the same period patient was treated with CAPROCIN, BAYASPIRIN. Patient was hospitalized.
Mytelase Side Effects Report #4827488-6
Mytelase side effect was reported by a Health Professional from FRANCE on Nov 02, 2005. Female patient, 39 years of age, weighting 158.7 lb, was diagnosed with myasthenic syndrome and was treated with Mytelase. After drug was administered, patient experienced the following side effects: cardio-respiratory arrest, cerebral disorder, cholinergic syndrome, pain. Mytelase dosage: unknown.
Mytelase Side Effects Report #4862883-0
Pharmacist from FRANCE reported Mytelase side effect on Dec 09, 2005. Female patient was diagnosed with myasthenic syndrome and was treated with Mytelase. After drug was administered, patient experienced the following side effects: myasthenia gravis neonatal. Mytelase dosage: unknown.
Mytelase Side Effects Report #4862885-4
Mytelase side effect was reported by a Pharmacist from FRANCE on Dec 09, 2005. Female patient was diagnosed with myasthenic syndrome and was treated with Mytelase. After drug was administered, patient experienced the following side effects: abortion induced, congenital lymphoedema, foetal malformation, skull malformation. Mytelase dosage: unknown. During the same period patient was treated with PAROXETINE, VITAMIN B. Patient died on 11/01/2005.
Mytelase Side Effects Report #4862893-3
Pharmacist from FRANCE reported Mytelase side effect on Dec 09, 2005. Female patient was diagnosed with myasthenic syndrome and was treated with Mytelase. After drug was administered, patient experienced the following side effects: polyhydramnios. Mytelase dosage: unknown.
Mytelase Side Effects Report #4862904-5
Mytelase side effect was reported by a Pharmacist from FRANCE on Dec 09, 2005. Female patient was diagnosed with myasthenic syndrome and was treated with Mytelase. After drug was administered, patient experienced the following side effects: abortion spontaneous. Mytelase dosage: unknown.
Mytelase Side Effects Report #4893614-6
Pharmacist from FRANCE reported Mytelase side effect on Dec 09, 2005. Female patient, 33 years of age, was diagnosed with myasthenic syndrome and was treated with Mytelase. After drug was administered, patient experienced the following side effects: abortion induced, foetal malformation, lymphoedema, skull malformation. Mytelase dosage: unknown. During the same period patient was treated with PAROXETINE, VITAMIN B.
Mytelase Side Effects Report #4917784-6
Mytelase side effect was reported by a Pharmacist from FRANCE on Dec 09, 2005. Female patient, 33 years of age, was diagnosed with myasthenic syndrome and was treated with Mytelase. After drug was administered, patient experienced the following side effects: abortion induced, foetal malformation. Mytelase dosage: unknown. During the same period patient was treated with PAROXETINE, VITAMIN B.
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Mytelase Side Effects Report #5618895-2
Consumer or non-health professional from FRANCE reported Mytelase side effect on Aug 17, 2007. Female patient, 43 years of age, was treated with Mytelase. After drug was administered, patient experienced the following side effects: back pain
, malaise, movement disorder , muscle spasms, pain in extremity, posture abnormal, speech disorder, vertigo. Mytelase dosage: 30 MG. Patient was hospitalized. Mytelase Side Effects Report #5661862-3
Mytelase side effect was reported by a Health Professional from JAPAN on Feb 29, 2008. Male patient was diagnosed with muscular weakness and was treated with Mytelase. After drug was administered, patient experienced the following side effects: cardio-respiratory arrest. Mytelase dosage: 15 MG.
Mytelase Side Effects Report #5740221-9
Health Professional from JAPAN reported Mytelase side effect on May 05, 2008. Male patient, 67 years of age, was diagnosed with myasthenia gravis and was treated with Mytelase. After drug was administered, patient experienced the following side effects: abdominal pain
, pancreatitis. Mytelase dosage: 20 MG. During the same period patient was treated with PYRIDOSTIGMINE BROMIDE, PYRIDOSTIGMINE BROMIDE. Patient was hospitalized. Mytelase Side Effects Report #5746907-4
Mytelase side effect was reported by a Health Professional from JAPAN on May 13, 2008. Male patient, 67 years of age, was diagnosed with myasthenia gravis and was treated with Mytelase. After drug was administered, patient experienced the following side effects: abdominal pain
, pancreatitis. Mytelase dosage: 20 MG. During the same period patient was treated with PYRIDOSTIGMINE BROMIDE, PYRIDOSTIGMINE BROMIDE. Patient was hospitalized. Mytelase Side Effects Report #5840480-8
Health Professional from JAPAN reported Mytelase side effect on July 30, 2008. Male patient, 55 years of age, was diagnosed with muscular weakness and was treated with Mytelase. After drug was administered, patient experienced the following side effects: brugada syndrome, bundle branch block right, electrocardiogram st segment elevation, loss of consciousness, ventricular extrasystoles, ventricular fibrillation. Mytelase dosage: 20 MG. Patient was hospitalized.
Mytelase Side Effects Report #6030274-5
Mytelase side effect was reported by a Pharmacist from FRANCE on Dec 29, 2008. Female patient, weighting 8.82 lb, was diagnosed with myasthenic syndrome and was treated with Mytelase. After drug was administered, patient experienced the following side effects: cholinergic syndrome, convulsion, diarrhoea, miosis, overdose, vomiting. Mytelase dosage: 2 MG. During the same period patient was treated with PERFALGAN, NEXIUM, PHOCYTAN, UVESTEROL.
Mytelase Side Effects Report #4608968-5
Consumer or non-health professional from reported Mytelase side effect on Jan 21, 2005. Male patient, 56 years of age, was diagnosed with myasthenia gravis and was treated with Mytelase. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, blood lactate dehydrogenase increased, thymectomy. Mytelase dosage: 20MG PO. During the same period patient was treated with CAPROCIN, BAYASPIRIN. Patient was hospitalized.
Mytelase Side Effects Report #4827488-6
Mytelase side effect was reported by a Health Professional from FRANCE on Nov 02, 2005. Female patient, 39 years of age, weighting 158.7 lb, was diagnosed with myasthenic syndrome and was treated with Mytelase. After drug was administered, patient experienced the following side effects: cardio-respiratory arrest, cerebral disorder, cholinergic syndrome, pain
. Mytelase dosage: unknown. Mytelase Side Effects Report #4862883-0
Pharmacist from FRANCE reported Mytelase side effect on Dec 09, 2005. Female patient was diagnosed with myasthenic syndrome and was treated with Mytelase. After drug was administered, patient experienced the following side effects: myasthenia gravis neonatal. Mytelase dosage: unknown.
Mytelase Side Effects Report #4862885-4
Mytelase side effect was reported by a Pharmacist from FRANCE on Dec 09, 2005. Female patient was diagnosed with myasthenic syndrome and was treated with Mytelase. After drug was administered, patient experienced the following side effects: abortion induced, congenital lymphoedema, foetal malformation, skull malformation. Mytelase dosage: unknown. During the same period patient was treated with PAROXETINE, VITAMIN B. Patient died on 11/01/2005.
Mytelase Side Effects Report #4862893-3
Pharmacist from FRANCE reported Mytelase side effect on Dec 09, 2005. Female patient was diagnosed with myasthenic syndrome and was treated with Mytelase. After drug was administered, patient experienced the following side effects: polyhydramnios. Mytelase dosage: unknown.
Mytelase Side Effects Report #4862904-5
Mytelase side effect was reported by a Pharmacist from FRANCE on Dec 09, 2005. Female patient was diagnosed with myasthenic syndrome and was treated with Mytelase. After drug was administered, patient experienced the following side effects: abortion spontaneous. Mytelase dosage: unknown.
Mytelase Side Effects Report #4893614-6
Pharmacist from FRANCE reported Mytelase side effect on Dec 09, 2005. Female patient, 33 years of age, was diagnosed with myasthenic syndrome and was treated with Mytelase. After drug was administered, patient experienced the following side effects: abortion induced, foetal malformation, lymphoedema, skull malformation. Mytelase dosage: unknown. During the same period patient was treated with PAROXETINE, VITAMIN B.
Mytelase Side Effects Report #4917784-6
Mytelase side effect was reported by a Pharmacist from FRANCE on Dec 09, 2005. Female patient, 33 years of age, was diagnosed with myasthenic syndrome and was treated with Mytelase. After drug was administered, patient experienced the following side effects: abortion induced, foetal malformation. Mytelase dosage: unknown. During the same period patient was treated with PAROXETINE, VITAMIN B.
