Original and hypertension Patient Reports February 12, 2012

Original Side Effects Report #4600435-8
Original side effect was reported by a Consumer or non-health professional from on Feb 23, 2005. Female patient, 71 years of age, weighting 140.0 lb, was diagnosed with myocardial infarction, prophylaxis and was treated with Original. After drug was administered, patient experienced the following side effects: cerebrovascular accident, hypertension. Original dosage: 325 MG, QD, ORAL. During the same period patient was treated with ORIGINAL BAYER. Patient was hospitalized. Patient recovered.

Original Side Effects Report #4618625-7
Original side effect was reported by a Consumer or non-health professional from on Mar 14, 2005. Female patient, 71 years of age, weighting 140.0 lb, was diagnosed with myocardial infarction, prophylaxis and was treated with Original. After drug was administered, patient experienced the following side effects: dizziness , hypertension, ischaemic stroke, thrombotic stroke. Original dosage: 325 MG, QD, ORAL. During the same period patient was treated with ORIGINAL BAYER, GLUCOPHAGE, LOTREL. Patient was hospitalized. Patient recovered.

Original Side Effects Report #5217014-4
Original side effect was reported by a Consumer or non-health professional from UNITED STATES on Jan 16, 2007. Female patient, 52 years of age, weighting 160.9 lb, was diagnosed with laxative supportive care and was treated with Original. After drug was administered, patient experienced the following side effects: dizziness , dreamy state, dyspnoea, hypertension, nausea , thinking abnormal, throat tightness, visual acuity reduced. Original dosage: TOTAL DAILY DOSE: 325 MG UNIT DOSE: 325 MG. During the same period patient was treated with CARDIZEM, HYDROCHLOROTHIAZIDE, MOTRIN, TYLENOL, LEVAQUIN. Patient recovered.

Original Side Effects Report #5264476-2
Original side effect was reported by a Consumer or non-health professional from UNITED STATES on Mar 12, 2007. Female patient, 52 years of age, weighting 160.9 lb, was diagnosed with laxative supportive care and was treated with Original. After drug was administered, patient experienced the following side effects: dizziness , dreamy state, dyspnoea, hypertension, nausea , thinking abnormal, throat tightness, visual acuity reduced. Original dosage: TOTAL DAILY DOSE: 325 MG UNIT DOSE: 325 MG. During the same period patient was treated with CARDIZEM, HYDROCHLOROTHIAZIDE, MOTRIN, TYLENOL, LEVAQUIN. Patient recovered.


Original Side Effects Report #5944800-5
Original side effect was reported by a Consumer or non-health professional from UNITED STATES on Oct 30, 2008. Female patient, 82 years of age, weighting 97.00 lb, was diagnosed with flatulence and was treated with Original. After drug was administered, patient experienced the following side effects: dizziness , headache , hypertension. Original dosage: unknown. During the same period patient was treated with ASPIRIN. Patient recovered.

Original Side Effects Report #6010857-9
Original side effect was reported by a Consumer or non-health professional from UNITED STATES on Dec 12, 2008. Female patient, 82 years of age, weighting 97.00 lb, was diagnosed with flatulence and was treated with Original. After drug was administered, patient experienced the following side effects: dizziness , headache , hypertension. Original dosage: unknown. During the same period patient was treated with ASPIRIN. Patient recovered.