Norpace and condition aggravated Patient Reports February 11, 2012

Norpace Side Effects Report #4595220-X
Norpace side effect was reported by a Health Professional from on Feb 11, 2005. Female patient was diagnosed with ventricular arrhythmia, arthritis , blood cholesterol increased and was treated with Norpace. After drug was administered, patient experienced the following side effects: arthralgia, arthritis , cerebrovascular accident, condition aggravated, dyspepsia, gastrointestinal haemorrhage, systemic lupus erythematosus. Norpace dosage: 450 MG (150 MG, 3 IN 1 D), ORAL. During the same period patient was treated with DAYPRO, PROCAINAMIDE, HMG COA REDUCTASE INHIBITORS, DYAZIDE, ACETAMINOPHEN. Patient recovered.

Norpace Side Effects Report #4653160-1
Norpace side effect was reported by a Physician from on Apr 25, 2005. Male patient, 71 years of age, weighting 160.0 lb, was diagnosed with atrial fibrillation  and was treated with Norpace. After drug was administered, patient experienced the following side effects: asthenia, atrial fibrillation , condition aggravated, flushing. Norpace dosage: 750 MG (150 MG, 5XDAY INTERVAL: EVERY DAY). During the same period patient was treated with PROPRANOLOL HYDROCHLORIDE, DIGOXIN, GEMFIBROZIL, ASPIRIN. Patient recovered.