Original and condition aggravated Patient Reports February 12, 2012

Original Side Effects Report #4684561-3
Original side effect was reported by a Consumer or non-health professional from on May 26, 2005. Male patient, 81 years of age, weighting 198.0 lb, was diagnosed with gastrointestinal disorder and was treated with Original. After drug was administered, patient experienced the following side effects: condition aggravated, gastrointestinal disorder, stomach discomfort. Original dosage: 325-650 MG, QD, ORAL; A FEW WEEKS. During the same period patient was treated with BLOOD THINNER, SLEEP AID. Patient recovered.

Original Side Effects Report #4727100-0
Original side effect was reported by a Consumer or non-health professional from UNITED STATES on July 12, 2005. Male patient, 81 years of age, weighting 198.0 lb, was diagnosed with dyspepsia and was treated with Original. After drug was administered, patient experienced the following side effects: condition aggravated, diverticulitis, dyspepsia, gastritis, stomach discomfort. Original dosage: 325 - 650MG, QD, ORAL/ A FEW WEEKS. During the same period patient was treated with ASPIRIN, PLAVIX, SLEEP AID. Patient recovered.

Original Side Effects Report #4655425-6
Original side effect was reported by a Consumer or non-health professional from on Apr 27, 2005. Female patient, 22 years of age, weighting 176.0 lb, was treated with Original. After drug was administered, patient experienced the following side effects: affective disorder, benign intracranial hypertension, blood pressure decreased, blood pressure increased, caesarean section, condition aggravated. Original dosage: unknown. During the same period patient was treated with COUMADIN, DIAMOX, CALCIUM WITH VITAMIN D, PROTONIX. Patient recovered.