Original Side Effects
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Original Side Effects reported on Patientsville.com
None reported at this time.Original Side Effects reported to FDA
Original Side Effects Report #5212923-4
Health Professional from UNITED STATES reported Original side effect on Jan 12, 2007. Female patient, 23 years of age, weighting 160.9 lb, was diagnosed with abdominal pain upper and was treated with Original. After drug was administered, patient experienced the following side effects: bloody discharge. Original dosage: TOTAL DAILY DOSE: 650 MG UNIT DOSE: 325 MG. During the same period patient was treated with PRENATAL VITAMINS. 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
Consumer or non-health professional from UNITED STATES reported Original side effect 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 #5280081-6
Original side effect was reported by a Consumer or non-health professional from UNITED STATES on Mar 20, 2007. Male patient, 67 years of age, weighting 149.9 lb, was diagnosed with dyspepsia and was treated with Original. After drug was administered, patient experienced the following side effects: dependence. Original dosage: unknown. During the same period patient was treated with STORE BRAND VITAMINS. Patient recovered.
Original Side Effects Report #5318577-0
Consumer or non-health professional from UNITED STATES reported Original side effect on May 01, 2007. Male patient, 43 years of age, weighting 180.8 lb, was diagnosed with stomach discomfort and was treated with Original. After drug was administered, patient experienced the following side effects: blood potassium increased, myocardial infarction. Original dosage: AS USED: 325 MG UNIT DOSE: 325 MG. Patient recovered.
Original Side Effects Report #5353513-2
Original side effect was reported by a Consumer or non-health professional from UNITED STATES on June 04, 2007. Male patient, 64 years of age, weighting 224.9 lb, was diagnosed with ischaemic heart disease prophylaxis and was treated with Original. After drug was administered, patient experienced the following side effects: feeling abnormal, heart rate increased, nervousness. Original dosage: TOTAL DAILY DOSE: 325 MG UNIT DOSE: 325 MG. During the same period patient was treated with ORIGINAL ALKA SELTZER, LISINOPRIL, PRILOSEC, NIACIN. Patient was hospitalized. Patient recovered.
Original Side Effects Report #5100868-X
Consumer or non-health professional from UNITED STATES reported Original side effect on May 31, 2006. Male patient, weighting 185.2 lb, was diagnosed with dyspepsia, nasopharyngitis and was treated with Original. After drug was administered, patient experienced the following side effects: blood glucose increased. Original dosage: TOTAL DAILY DOSE: 650 MG UNIT DOSE: 325 MG. During the same period patient was treated with HUMULIN. Patient recovered.
Original Side Effects Report #5104458-4
Original side effect was reported by a Consumer or non-health professional from UNITED STATES on Sept 02, 2006. Female patient, 23 years of age, weighting 160.9 lb, was diagnosed with abdominal pain upper and was treated with Original. After drug was administered, patient experienced the following side effects: bloody discharge. Original dosage: TOTAL DAILY DOSE: 650 MG UNIT DOSE: 325 MG. During the same period patient was treated with PRENATAL VITAMINS. Patient recovered.
Original Side Effects Report #5115512-5
Consumer or non-health professional from UNITED STATES reported Original side effect on July 07, 2006. Male patient, 52 years of age, weighting 205.0 lb, was diagnosed with dyspepsia and was treated with Original. After drug was administered, patient experienced the following side effects: abdominal pain
, nephrolithiasis. Original dosage: UNIT DOSE: 325 MG. Patient recovered.Original Side Effects Report #5153771-3
Original side effect was reported by a Consumer or non-health professional from UNITED STATES on Nov 14, 2006. Male patient, 46 years of age, weighting 224.9 lb, was diagnosed with dyspepsia and was treated with Original. After drug was administered, patient experienced the following side effects: blood urine present, calculus ureteric, flank pain, nephrolithiasis. Original dosage: unknown. Patient recovered.
Original Side Effects Report #5389052-2
Consumer or non-health professional from UNITED STATES reported Original side effect on July 16, 2007. Male patient, 43 years of age, weighting 180.8 lb, was diagnosed with stomach discomfort and was treated with Original. After drug was administered, patient experienced the following side effects: blood potassium increased, myocardial infarction. Original dosage: AS USED: 325 MG UNIT DOSE: 325 MG. Patient recovered.
Original Side Effects Report #5414995-0
Original side effect was reported by a Consumer or non-health professional from UNITED STATES on Aug 08, 2007. Male patient, 64 years of age, weighting 224.9 lb, was diagnosed with cardiovascular event prophylaxis and was treated with Original. After drug was administered, patient experienced the following side effects: anxiety
, feeling abnormal, heart rate increased, nervousness. Original dosage: TOTAL DAILY DOSE: 325 MG UNIT DOSE: 325 MG. During the same period patient was treated with ORIGINAL ALKA SELTZER, CENTRUM CHEWABLE, LISINOPRIL, PRILOSEC, NIACIN. Patient was hospitalized. Patient recovered.Original Side Effects Report #5451093-4
Physician from UNITED STATES reported Original side effect on Sept 05, 2007. Male patient, 64 years of age, weighting 224.9 lb, was diagnosed with cardiovascular event prophylaxis and was treated with Original. After drug was administered, patient experienced the following side effects: anxiety
, chest pain , feeling abnormal, heart rate increased, nervousness. Original dosage: TOTAL DAILY DOSE: 325 MG UNIT DOSE: 325 MG. During the same period patient was treated with ORIGINAL ALKA SELTZER, CENTRUM CHEWABLE, ISOTONIX OPX, LISINOPRIL, PRILOSEC, NIACIN, RICE, DOXAZOSIN MESYLATE. 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
Consumer or non-health professional from UNITED STATES reported Original side effect 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 #5687528-1
Original side effect was reported by a Consumer or non-health professional from UNITED STATES on Mar 18, 2008. Female patient, 54 years of age, weighting 145.5 lb, was treated with Original. After drug was administered, patient experienced the following side effects: haematemesis. Original dosage: unknown. During the same period patient was treated with NEXIUM, PLAVIX, LIPITOR. Patient recovered.
Original Side Effects Report #5740726-0
Consumer or non-health professional from UNITED STATES reported Original side effect on May 02, 2008. Female patient, 54 years of age, weighting 145.5 lb, was treated with Original. After drug was administered, patient experienced the following side effects: haematemesis. Original dosage: unknown. During the same period patient was treated with NEXIUM, PLAVIX, LIPITOR. 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 #5798100-7
Consumer or non-health professional from UNITED STATES reported Original side effect on June 23, 2008. Female patient, 53 years of age, weighting 200.6 lb, was diagnosed with dyspepsia and was treated with Original. After drug was administered, patient experienced the following side effects: alopecia, blood pressure increased, dyspepsia, fluid retention, gastrooesophageal reflux disease. Original dosage: unknown. During the same period patient was treated with ORIGINAL ALKA. Patient recovered.
Original Side Effects Report #5821168-6
Original side effect was reported by a Consumer or non-health professional from UNITED STATES on July 10, 2008. Male patient, 76 years of age, weighting 180.8 lb, was diagnosed with dyspepsia and was treated with Original. After drug was administered, patient experienced the following side effects: dyspepsia, oesophageal carcinoma. Original dosage: unknown. Patient recovered.
Original Side Effects Report #5835102-6
Consumer or non-health professional from UNITED STATES reported Original side effect on July 23, 2008. Female patient, 54 years of age, weighting 145.5 lb, was treated with Original. After drug was administered, patient experienced the following side effects: haematemesis. Original dosage: unknown. During the same period patient was treated with NEXIUM, PLAVIX, LIPITOR. Patient recovered.
Original Side Effects Report #5876283-8
Original side effect was reported by a Consumer or non-health professional from UNITED STATES on Sept 03, 2008. Female patient, 53 years of age, weighting 200.6 lb, was diagnosed with dyspepsia and was treated with Original. After drug was administered, patient experienced the following side effects: alopecia, blood pressure increased, dyspepsia, fluid retention, gastrooesophageal reflux disease, local swelling. Original dosage: unknown. During the same period patient was treated with ORIGINAL ALKA. Patient recovered.
Original Side Effects Report #5944800-5
Consumer or non-health professional from UNITED STATES reported Original side effect 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.Original Side Effects Report #6022626-4
Consumer or non-health professional from UNITED STATES reported Original side effect on Dec 29, 2008. Male patient, 76 years of age, weighting 180.8 lb, was diagnosed with dyspepsia and was treated with Original. After drug was administered, patient experienced the following side effects: dyspepsia, oesophageal carcinoma. Original dosage: unknown. Patient recovered.
Original Side Effects Report #6061272-3
Original side effect was reported by a Consumer or non-health professional from UNITED STATES on Jan 19, 2009. Female patient, 92 years of age, weighting 149.9 lb, was diagnosed with laxative supportive care and was treated with Original. After drug was administered, patient experienced the following side effects: diarrhoea, eructation, malaise, nausea
, weight decreased. Original dosage: unknown. During the same period patient was treated with PLENDIL, ZOCOR, MAXZIDE, AGGRENOX. Patient was hospitalized. Patient recovered.Original Side Effects Report #6061787-8
Consumer or non-health professional from UNITED STATES reported Original side effect on Jan 26, 2009. Male patient, 28 years of age, weighting 180.8 lb, was diagnosed with dyspepsia and was treated with Original. After drug was administered, patient experienced the following side effects: abdominal pain upper, gastric ulcer, haematemesis, vomiting. Original dosage: unknown. During the same period patient was treated with CARAFATE, ZANTAC, PRILOSEC. Patient recovered.
Original Side Effects Report #6077072-4
Original side effect was reported by a Consumer or non-health professional from UNITED STATES on Feb 09, 2009. Female patient, 92 years of age, weighting 149.9 lb, was diagnosed with laxative supportive care and was treated with Original. After drug was administered, patient experienced the following side effects: diarrhoea, eructation, malaise, nausea
, weight decreased. Original dosage: unknown. During the same period patient was treated with PLENDIL, ZOCOR, MAXZIDE, AGGRENOX. Patient was hospitalized. Patient recovered.Original Side Effects Report #4547116-7
Consumer or non-health professional from reported Original side effect 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.
Original Side Effects Report #4600435-8
Consumer or non-health professional from reported Original side effect 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 #4600438-3
Original side effect was reported by a Consumer or non-health professional from on Feb 23, 2005. Male patient, child 6 years of age, weighting 42.00 lb, was diagnosed with nasopharyngitis and was treated with Original. After drug was administered, patient experienced the following side effects: amnesia, confusional state, depressed level of consciousness, dysstasia. Original dosage: 325/1916 MG, ONCE, ORAL. Patient recovered.
Original Side Effects Report #4618625-7
Consumer or non-health professional from reported Original side effect 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 #4628250-X
Original side effect was reported by a Consumer or non-health professional from on Mar 21, 2005. Male patient, 40 years of age, weighting 265.0 lb, was diagnosed with nasopharyngitis and was treated with Original. After drug was administered, patient experienced the following side effects: asthma
, contraindication to medical treatment, respiratory arrest, respiratory distress. Original dosage: 650 MG, ONCE, ORAL. During the same period patient was treated with FIORINAL W, PREDNISONE. Patient recovered.Original Side Effects Report #4635231-9
Consumer or non-health professional from reported Original side effect on Apr 04, 2005. Male patient, 59 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: full blood count decreased. Original dosage: 5200 MG, TOTAL DAILY, ORAL. During the same period patient was treated with METFORMIN, SIMVASTATIN, OMEPRAZOLE, FOLIC ACID. Patient was hospitalized. Patient recovered.
Original Side Effects Report #4635322-2
Original side effect was reported by a Consumer or non-health professional from on Apr 01, 2005. Male patient, 49 years of age, weighting 195.0 lb, was treated with Original. After drug was administered, patient experienced the following side effects: deafness unilateral. Original dosage: 650 MG, BID, ORAL. During the same period patient was treated with ATENOLOL. Patient recovered.
Original Side Effects Report #4648772-5
Consumer or non-health professional from reported Original side effect on Apr 20, 2005. Male patient, child 6 years of age, weighting 42.00 lb, was diagnosed with nasopharyngitis and was treated with Original. After drug was administered, patient experienced the following side effects: abasia, confusional state, hypersomnia, memory impairment. Original dosage: 325/1915 MG, ONCE, ORAL. Patient died.
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.
Original Side Effects Report #4668460-9
Consumer or non-health professional from reported Original side effect on May 13, 2005. Male patient, 49 years of age, weighting 195.0 lb, was diagnosed with dyspepsia and was treated with Original. After drug was administered, patient experienced the following side effects: deafness unilateral. Original dosage: 650 MG, BID, ORAL. During the same period patient was treated with ATENOLOL. Patient recovered.
Original Side Effects Report #4681217-8
Original side effect was reported by a Consumer or non-health professional from on May 19, 2005. Male patient, 61 years of age, weighting 260.0 lb, was diagnosed with dyspepsia and was treated with Original. After drug was administered, patient experienced the following side effects: benign prostatic hyperplasia, cholelithiasis, myocardial infarction, nephrolithiasis. Original dosage: unknown. During the same period patient was treated with ADVIL, SENIOR VITAMINS, POTASSIUM CHLORIDE. Patient recovered.
Original Side Effects Report #4684561-3
Consumer or non-health professional from reported Original side effect 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 #4698679-2
Original side effect was reported by a Consumer or non-health professional from on June 17, 2005. Female patient, 75 years of age, weighting 150.0 lb, was diagnosed with myocardial infarction, prophylaxis and was treated with Original. After drug was administered, patient experienced the following side effects: dizziness
, myocardial infarction, stomach discomfort. Original dosage: 325 MG, QD; ORAL. During the same period patient was treated with ORIGINAL BAYER ASPIRIN, PLAVIX. Patient recovered.Original Side Effects Report #4704185-9
Consumer or non-health professional from reported Original side effect on June 21, 2005. Male patient, 61 years of age, weighting 260.0 lb, was diagnosed with dyspepsia and was treated with Original. After drug was administered, patient experienced the following side effects: benign prostatic hyperplasia, cholelithiasis, myocardial infarction, nephrolithiasis. Original dosage: unknown. During the same period patient was treated with ADVIL, SENIOR VITAMINS, POTASSIUM CHLORIDE. 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 #4753176-0
Consumer or non-health professional from UNITED STATES reported Original side effect 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 #4822043-6
Original side effect was reported by a Consumer or non-health professional from UNITED STATES on Oct 24, 2005. Male patient, 70 years of age, weighting 165.0 lb, was diagnosed with dyspepsia and was treated with Original. After drug was administered, patient experienced the following side effects: blood phosphorus increased. Original dosage: 650 MG, ORAL. During the same period patient was treated with COREG, NORVASC, PRAVACHOL, IMDUR, OMEPRAZOLE, RENAGEL, HYTRIN. Patient recovered.
Original Side Effects Report #4866046-4
Consumer or non-health professional from UNITED STATES reported Original side effect on Dec 05, 2005. Male patient, 67 years of age, weighting 198.0 lb, was diagnosed with dyspepsia, flatulence, prophylaxis and was treated with Original. After drug was administered, patient experienced the following side effects: blood glucose fluctuation. Original dosage: unknown. During the same period patient was treated with ORIGINAL ALKA SELZER, ORIGINAL ALKA SELZER, PLAVIX, CELEXA, PRAVACHOL, PROTONIX, EQUATE ASPIRIN, BETAPACE. Patient recovered.
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