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Betapace Safety Reports
Total Betapace reports: 13.Betapace FDA safety alerts: No.
Reported deaths: 1 Reported hospitalizations: 7.
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Reported Betapace Side Effects: atrial fibrillation, blood sodium decreased, speech disorder, hemiparesis, confusional state, pericardial effusion, palpitations, nausea, headache, dysphagia, depression.
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Betapace Side Effects Report #5221417-1
Consumer or non-health professional from UNITED STATES reported BETAPACE problem on Jan 19, 2007. Male patient, 54 years of age, was treated with BETAPACE. After drug was administered, patient experienced the following problems/side effects: confusional state, hemiparesis, speech disorder. BETAPACE dosage: 80 MG, UNK. During the same period patient was treated with AVAPRO, COUMADIN. Patient was hospitalized. Patient recovered.
Betapace Side Effects Report #5281312-9
BETAPACE problem was reported by a Physician from UNITED STATES on July 11, 2006. Male patient was diagnosed with atrial fibrillation and was treated with BETAPACE. After drug was administered, patient experienced the following problems/side effects: atrial fibrillation, supraventricular extrasystoles. BETAPACE dosage: unknown. Patient recovered.
Betapace Side Effects Report #5295803-8
Health Professional from UNITED STATES reported BETAPACE problem on Apr 10, 2007. Female patient, 20 years of age, was treated with BETAPACE. After drug was administered, patient experienced the following problems/side effects: electrocardiogram qt prolonged, hypotension, pregnancy. BETAPACE dosage: unknown. During the same period patient was treated with ESMOLOL. Patient recovered.
Betapace Side Effects Report #5345152-4
BETAPACE problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 01, 2006. Female patient was diagnosed with atrial fibrillation and was treated with BETAPACE. After drug was administered, patient experienced the following problems/side effects: atrial fibrillation, fatigue, syncope. BETAPACE dosage: unknown. Patient was hospitalized. Patient recovered.
Betapace Side Effects Report #5066830-0
Physician from UNITED STATES reported BETAPACE problem on July 18, 2006. Female patient, 53 years of age, was treated with BETAPACE. After drug was administered, patient experienced the following problems/side effects: cardiac arrest, hypertension, hypoxic encephalopathy, pulmonary oedema. BETAPACE dosage: unknown. Patient was hospitalized. Patient died on 08/10/1992.
Betapace Side Effects Report #5074841-4
BETAPACE problem was reported by a Physician from UNITED STATES on May 17, 2006. Female patient, 89 years of age, weighting 110.0 lb, was diagnosed with heart rate irregular, blood cholesterol increased, hypertension and was treated with BETAPACE. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, depressed level of consciousness, hepatic enzyme increased, hepatic failure, hepatitis, lethargy. BETAPACE dosage: unknown. During the same period patient was treated with PRAVACHOL, TYLENOL W, DIOVAN HCT. Patient was hospitalized. Patient recovered.
Betapace Side Effects Report #5096985-3
Consumer or non-health professional from UNITED STATES reported BETAPACE problem on Aug 31, 2006. Female patient, 76 years of age, weighting 144.4 lb, was diagnosed with atrial fibrillation and was treated with BETAPACE. After drug was administered, patient experienced the following problems/side effects: atrial fibrillation, bradycardia, torsade de pointes. BETAPACE dosage: 80 MG BID PO. Patient recovered.
Betapace Side Effects Report #5142205-0
BETAPACE problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 18, 2006. Male patient, 54 years of age, was treated with BETAPACE. After drug was administered, patient experienced the following problems/side effects: confusional state, hemiparesis, speech disorder. BETAPACE dosage: 80 MG, ORAL. During the same period patient was treated with AVAPRO, COUMADIN. Patient was hospitalized. Patient recovered.
Betapace Side Effects Report #5148805-6
Pharmacist from UNITED STATES reported BETAPACE problem on Oct 27, 2006. Female patient was diagnosed with supraventricular tachycardia and was treated with BETAPACE. After drug was administered, patient experienced the following problems/side effects: hypothermia neonatal. BETAPACE dosage: unknown. Patient recovered.
Betapace Side Effects Report #5155619-X
BETAPACE problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 02, 2006. Male patient, 78 years of age, weighting 149.9 lb, was diagnosed with atrial fibrillation and was treated with BETAPACE. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased. BETAPACE dosage: 160 MG/D, ORAL. During the same period patient was treated with COUMADIN, SYNTHROID. Patient was hospitalized. Patient recovered.
Betapace Side Effects Report #5195572-6
Consumer or non-health professional from UNITED STATES reported BETAPACE problem on Dec 26, 2006. Male patient, 71 years of age, weighting 195.0 lb, was treated with BETAPACE. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, chest pain, coronary artery occlusion, gastrooesophageal reflux disease, oesophageal spasm. BETAPACE dosage: unknown. Patient recovered.
Betapace Side Effects Report #5391663-5
BETAPACE problem was reported by a Consumer or non-health professional from UNITED STATES on July 06, 2007. Male patient, 78 years of age, weighting 149.9 lb, was diagnosed with atrial fibrillation and was treated with BETAPACE. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased. BETAPACE dosage: 90 MG, 2X/DAY. During the same period patient was treated with COUMADIN, SYNTHROID. Patient was hospitalized. Patient recovered.
Betapace Side Effects Report #5428654-1
Physician from UNITED STATES reported BETAPACE problem on Aug 21, 2007. Female patient, 86 years of age, weighting 94.80 lb, was diagnosed with atrial fibrillation and was treated with BETAPACE. After drug was administered, patient experienced the following problems/side effects: asthenia, decreased appetite, depression, dysphagia, headache, nausea, palpitations, pericardial effusion. BETAPACE dosage: 80 MG, UNK. During the same period patient was treated with MAGNESIUM SULPHATE, VITAMIN, GADOLINIUM EOB. Patient recovered.