Original and dyspnoea Patient Reports February 12, 2012

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 #4753176-0
Original side effect was reported by a Consumer or non-health professional from UNITED STATES on Aug 10, 2005. Male patient, 58 years of age, weighting 250.0 lb, was diagnosed with dyspepsia and was treated with Original. After drug was administered, patient experienced the following side effects: dyspnoea, gastric ulcer, gastritis, rectal haemorrhage. Original dosage: 5200 MG, TOTAL DAILY, ORAL. During the same period patient was treated with ASPIRIN, METFORMIN, SIMVASTATIN, OMEPRAZOLE, FOLIC ACID, PRINIVIL, COMBIVENT. Patient was hospitalized. Patient recovered.

Original Side Effects Report #5598359-5
Original side effect was reported by a Consumer or non-health professional from UNITED STATES on Jan 07, 2008. Female patient, 38 years of age, weighting 194.0 lb, was diagnosed with constipation  and was treated with Original. After drug was administered, patient experienced the following side effects: blood cholesterol increased, cardiomegaly, diabetes mellitus, dyspnoea, renal failure, thyroid disorder, weight decreased. Original dosage: unknown. During the same period patient was treated with PHILLIPS LAXATIVE DIETARY SUPPLEMENT, MIRALAX, CASCARA SEGRADA. Patient recovered.


Original Side Effects Report #5610399-6
Original side effect was reported by a Consumer or non-health professional from UNITED STATES on Jan 07, 2008. Female patient, 38 years of age, weighting 195.0 lb, was diagnosed with constipation  and was treated with Original. After drug was administered, patient experienced the following side effects: blood cholesterol increased, cardiomegaly, diabetes mellitus, dyspnoea, renal failure, thyroid disorder, weight decreased. Original dosage: unknown. During the same period patient was treated with PHILLIPS LAXATIVE DIETARY SUPPLEMENT, MIRALAX, CASCARA SEGRADA. Patient recovered.

Original Side Effects Report #5779078-9
Original side effect was reported by a Consumer or non-health professional from UNITED STATES on June 10, 2008. Female patient, 38 years of age, weighting 194.0 lb, was diagnosed with constipation  and was treated with Original. After drug was administered, patient experienced the following side effects: blood cholesterol increased, cardiomegaly, cerebrovascular accident, diabetes mellitus, dyspnoea, dysuria, malignant hypertension, renal failure, thyroid disorder. Original dosage: unknown. During the same period patient was treated with PHILLIPS LAXATIVE DIETARY SUPPLEMENT, MIRALAX, CASCARA SEGRADA. Patient was hospitalized. Patient recovered.

Original Side Effects Report #4547116-7
Original side effect was reported by a Consumer or non-health professional from on Dec 21, 2004. Female patient, 21 years of age, weighting 176.0 lb, was treated with Original. After drug was administered, patient experienced the following side effects: benign intracranial hypertension, blood pressure decreased, caesarean section, dyspnoea, gastrooesophageal reflux disease, headache , intestinal obstruction. Original dosage: unknown. During the same period patient was treated with COUMADIN, DIAMOX, CALCIUM WITH VITAMIN D, PROTONIX. Patient recovered.

Original Side Effects Report #4548540-9
Original side effect was reported by a Consumer or non-health professional from on Dec 21, 2004. Female patient, 21 years of age, weighting 176.0 lb, was treated with Original. After drug was administered, patient experienced the following side effects: benign intracranial hypertension, blood pressure decreased, caesarean section, dyspnoea, gastrooesophageal reflux disease, intestinal obstruction, mood altered. Original dosage: unknown. During the same period patient was treated with COUMADIN, DIAMOX, CALCIUM WITH VITAMIN D, PROTONIX. Patient recovered.