Accupril and condition aggravated Patient Reports February 10, 2012
Accupril Side Effects Report #5271842-8
Accupril side effect was reported by a Health Professional from UNITED STATES on Mar 12, 2007. Female patient, weighting 149.9 lb, was diagnosed with renal disorder and was treated with Accupril. After drug was administered, patient experienced the following side effects: anaemia, bacteria urine, blood glucose abnormal, cells in urine, condition aggravated, haemoglobin urine present, renal impairment, urine leukocyte esterase positive. Accupril dosage: unknown. During the same period patient was treated with GLUCOTROL, LIPITOR. Patient recovered.
Accupril Side Effects Report #4862952-5
Accupril side effect was reported by a Consumer or non-health professional from UNITED STATES on Dec 06, 2005. Female patient, 79 years of age, weighting 158.0 lb, was diagnosed with hypertension, gingival infection, blood pressure
and was treated with Accupril. After drug was administered, patient experienced the following side effects: blood potassium decreased, blood pressure increased, cataract
, chest pain
, condition aggravated, dizziness
, dyspnoea. Accupril dosage: unknown. During the same period patient was treated with NORVASC, FLUORIDE, ZITHROMAX, TOPROL, VITAMIN B CAP, VITAMIN C, VITAMIN E. Patient died.Accupril Side Effects Report #4546352-3
Accupril side effect was reported by a Consumer or non-health professional from on Dec 22, 2004. Female patient, 73 years of age, was diagnosed with hypertension, condition aggravated, osteoarthritis
and was treated with Accupril. After drug was administered, patient experienced the following side effects: activities of daily living impaired, asthenia, bedridden, body height decreased, cardiac fibrillation, condition aggravated, dyspnoea, fatigue, impaired driving ability. Accupril dosage: 40 MG (40 MG, 1 IN 1 D), ORAL. During the same period patient was treated with NORVASC, ARTHROTEC, ATENOLOL, CODEINE PHOSPHATE AND ACETAMINOPHEN, POTASSIUM, CALCIUM. Patient recovered.Accupril Side Effects Report #4618886-4
Accupril side effect was reported by a Consumer or non-health professional from on Feb 21, 2005. Female patient, 73 years of age, was diagnosed with hypertension, condition aggravated, osteoarthritis
and was treated with Accupril. After drug was administered, patient experienced the following side effects: activities of daily living impaired, asthenia, back disorder, body height decreased, cachexia, cardiac fibrillation, condition aggravated, dyspnoea. Accupril dosage: 40 MG (40 MG, 1 IN 1 D), ORAL. During the same period patient was treated with NORVASC, ARTHROTEC, ATENOLOL, CODEINE PHOSPHATE AND ACETAMINOPHEN, POTASSIUM ACETATE, CALCIUM, THYROID. Patient recovered.Accupril Side Effects Report #4618886-4
Accupril side effect was reported by a Consumer or non-health professional from on Feb 21, 2005. Female patient, 73 years of age, was diagnosed with hypertension, condition aggravated, osteoarthritis
and was treated with Accupril. After drug was administered, patient experienced the following side effects: activities of daily living impaired, asthenia, back disorder, body height decreased, cachexia, cardiac fibrillation, condition aggravated, dyspnoea. Accupril dosage: 40 MG (40 MG, 1 IN 1 D), ORAL. During the same period patient was treated with NORVASC, ARTHROTEC, ATENOLOL, CODEINE PHOSPHATE AND ACETAMINOPHEN, POTASSIUM ACETATE, CALCIUM, THYROID. Patient recovered.Accupril Side Effects Report #4916079-4
Accupril side effect was reported by a Physician from UNITED STATES on Feb 02, 2006. Male patient, 53 years of age, weighting 553.4 lb, was diagnosed with hypertension, ill-defined disorder, schizophrenia and was treated with Accupril. After drug was administered, patient experienced the following side effects: abnormal behaviour, condition aggravated, convulsion, mental disorder. Accupril dosage: 20 MG (20 MG, 1 IN 1 D). During the same period patient was treated with HYDROCHLOROTHIAZIDE, CLOZARIL, DEPAKOTE, FELDENE, DITROPAN, BISACODYL, BACLOFEN. Patient died on 09/11/2003.
Accupril Side Effects Report #4737379-7
Accupril side effect was reported by a Consumer or non-health professional from UNITED STATES on July 25, 2005. Male patient, 51 years of age, weighting 166.0 lb, was diagnosed with hypertension, blood cholesterol increased, emphysema and was treated with Accupril. After drug was administered, patient experienced the following side effects: arterial occlusive disease, carotid artery occlusion, condition aggravated, emphysema, skin discolouration. Accupril dosage: 20 MG (20 MG, DAILY INTERVAL: EVERY DAY), ORAL. During the same period patient was treated with LIPITOR, TIOTROPIUM BROMIDE, DURAGESIC, NITRODUR II, NITROGLYCERIN, OXYCODONE, ALBUTEROL, IPRATROPIUM BROMIDE. Patient recovered.
Accupril Side Effects Report #5333983-6
Accupril side effect was reported by a Health Professional from UNITED STATES on May 15, 2007. Female patient, weighting 149.9 lb, was diagnosed with hypertension, diabetes mellitus non-insulin-dependent and was treated with Accupril. After drug was administered, patient experienced the following side effects: anaemia, bacteria urine, blood glucose abnormal, cells in urine, condition aggravated, haemoglobin urine present, renal impairment, urine leukocyte esterase positive. Accupril dosage: unknown. During the same period patient was treated with GLUCOTROL, LIPITOR. Patient recovered.
Accupril Side Effects Report #4834813-9
Accupril side effect was reported by a Consumer or non-health professional from UNITED STATES on Nov 03, 2005. Female patient, weighting 158.0 lb, was diagnosed with hypertension, blood pressure
and was treated with Accupril. After drug was administered, patient experienced the following side effects: cataract
, condition aggravated, dyspnoea, flatulence, hypertension, myocardial infarction, ocular vascular disorder, oedema peripheral, vision blurred. Accupril dosage: 20 MG (20 MG, 1 IN 1 D). During the same period patient was treated with TOPROL. Patient recovered.Accupril Side Effects Report #4973020-6
Accupril side effect was reported by a Consumer or non-health professional from UNITED STATES on Mar 29, 2006. Female patient, weighting 150.0 lb, was diagnosed with hypertension and was treated with Accupril. After drug was administered, patient experienced the following side effects: anxiety
, back pain
, condition aggravated, hypertension, panic attack. Accupril dosage: unknown. During the same period patient was treated with ACCURETIC, NORVASC, HYDROCHLOROTHIAZIDE. Patient was hospitalized. Patient recovered.Accupril Side Effects Report #4973936-0
Accupril side effect was reported by a Consumer or non-health professional from UNITED STATES on Mar 31, 2006. Female patient, weighting 130.0 lb, was diagnosed with hypertension and was treated with Accupril. After drug was administered, patient experienced the following side effects: arthritis
, condition aggravated, decreased activity, depression
, fibromyalgia, immune system disorder, knee arthroplasty, nasopharyngitis, pain
. Accupril dosage: 40 MG (40 MG, DAILY). During the same period patient was treated with PRAVACHOL, TRICOR, LEXAPRO, PREDNISONE, VALIUM, QUININE SULPHATE, RITALIN. Patient was hospitalized and became disabled. Patient recovered.Accupril Side Effects Report #4999174-3
Accupril side effect was reported by a Consumer or non-health professional from UNITED STATES on May 02, 2006. Male patient, weighting 142.0 lb, was diagnosed with hypertension, depression
and was treated with Accupril. After drug was administered, patient experienced the following side effects: anorexia, blood creatinine increased, blood urea increased, condition aggravated, depression
, hypertension, renal disorder, weight decreased. Accupril dosage: unknown. During the same period patient was treated with PROZAC, ACETYLSALICYLIC ACID SRT, FOLIC ACID, PRAVACHOL. Patient recovered.Accupril Side Effects Report #4963649-3
Accupril side effect was reported by a Physician from POLAND on Mar 21, 2006. Female patient, 72 years of age, weighting 158.7 lb, was diagnosed with cardiac failure and was treated with Accupril. After drug was administered, patient experienced the following side effects: asthenia, atrioventricular block second degree, cardiac failure congestive, condition aggravated, hyperkalaemia, palpitations, vertigo. Accupril dosage: unknown. During the same period patient was treated with SPIRONOLACTONE, POTASSIUM CHLORIDE, AMARYL, GLUCOBAY, CONCOR COR. Patient was hospitalized. Patient recovered.
Accupril Side Effects Report #4983284-0
Accupril side effect was reported by a Physician from POLAND on Apr 11, 2006. Female patient, 72 years of age, weighting 158.7 lb, was diagnosed with cardiac failure and was treated with Accupril. After drug was administered, patient experienced the following side effects: asthenia, atrioventricular block second degree, cardiac failure congestive, condition aggravated, hyperkalaemia, palpitations, vertigo. Accupril dosage: (10 MG, QD), ORAL. During the same period patient was treated with SPIRONOLACTONE, POTASSIUM CHLORIDE, AMARYL, GLUCOBAY, CONCOR COR. Patient was hospitalized. Patient recovered.
Accupril Side Effects Report #4656351-9
Accupril side effect was reported by a Physician from on May 16, 2002. Female patient, 62 years of age, weighting 165.3 lb, was treated with Accupril. After drug was administered, patient experienced the following side effects: arteriosclerosis, azotaemia, cardiac failure congestive, cholecystitis, cholelithiasis, chronic obstructive pulmonary disease, condition aggravated, diplopia. Accupril dosage: unknown. During the same period patient was treated with LEVAQUIN, PROTONIX. Patient was hospitalized. Patient recovered.
Accupril Side Effects Report #5195735-X
Accupril side effect was reported by a Physician from UNITED STATES on Dec 22, 2006. Female patient, 37 years of age, was treated with Accupril. After drug was administered, patient experienced the following side effects: bile duct stone, biliary tract disorder, blood glucose increased, condition aggravated, dysphagia, ejection fraction decreased, electrophoresis protein abnormal, feeling abnormal. Accupril dosage: unknown. During the same period patient was treated with LANTUS, NOVOLOG, GLUCOPHAGE, LIPITOR, ACTOS, NEXIUM. Patient recovered.
Accupril and condition aggravated 