Cozaar and platelet count decreased Patient Reports February 10, 2012
Cozaar Side Effects Report #4835292-8
Cozaar side effect was reported by a Physician from JAPAN on Oct 31, 2005. Female patient, 67 years of age, weighting 127.9 lb, was diagnosed with ventricular remodeling, hypertension, insomnia, constipation prophylaxis, pulmonary artery dilatation and was treated with Cozaar. After drug was administered, patient experienced the following side effects: pancytopenia, platelet count decreased, pyrexia. Cozaar dosage: unknown. During the same period patient was treated with ROHYPNOL, HEPARIN, ALDACTONE, MAGNESIUM OXIDE, PROCYLIN. Patient was hospitalized. Patient recovered.
Cozaar Side Effects Report #4564510-9
Cozaar side effect was reported by a Consumer or non-health professional from on Jan 12, 2005. Male patient, 72 years of age, was diagnosed with hypertension and was treated with Cozaar. After drug was administered, patient experienced the following side effects: atrial fibrillation
, blood cholesterol increased, blood lactate dehydrogenase increased, blood potassium decreased, cardiac failure, platelet count decreased, ventricular hypertrophy. Cozaar dosage: 50MG/DAILY. During the same period patient was treated with HERBESSER, NORMONAL, NORVASC. Patient was hospitalized. Patient recovered.Cozaar Side Effects Report #4682506-3
Cozaar side effect was reported by a Physician from on May 26, 2005. Female patient, 71 years of age, was diagnosed with hypertension, viraemia, hepatic function abnormal and was treated with Cozaar. After drug was administered, patient experienced the following side effects: cerebral haemorrhage, platelet count decreased. Cozaar dosage: unknown. During the same period patient was treated with GLYCYRON. Patient recovered.
Cozaar Side Effects Report #4699849-X
Cozaar side effect was reported by a Physician from on June 14, 2005. Female patient, 60 years of age, weighting 121.3 lb, was diagnosed with hypertension, fibromyalgia and was treated with Cozaar. After drug was administered, patient experienced the following side effects: haemorrhage subcutaneous, platelet count decreased, thrombocytopenia. Cozaar dosage: unknown. During the same period patient was treated with NICARDIPINE, PREDONINE. Patient was hospitalized. Patient recovered.
Cozaar Side Effects Report #4749729-6
Cozaar side effect was reported by a Physician from JAPAN on Aug 12, 2005. Male patient, 56 years of age, was diagnosed with hypertension, diabetes mellitus and was treated with Cozaar. After drug was administered, patient experienced the following side effects: nasopharyngitis, platelet count decreased. Cozaar dosage: unknown. During the same period patient was treated with BASEN, PREDONINE, COTRIM. Patient recovered.
Cozaar Side Effects Report #4751901-6
Cozaar side effect was reported by a Physician from JAPAN on Aug 12, 2005. Male patient, 56 years of age, was diagnosed with hypertension, diabetes mellitus and was treated with Cozaar. After drug was administered, patient experienced the following side effects: nasopharyngitis, platelet count decreased. Cozaar dosage: unknown. During the same period patient was treated with BASEN, PREDONINE, COTRIM. Patient recovered.
Cozaar Side Effects Report #4761951-1
Cozaar side effect was reported by a Physician from JAPAN on Aug 12, 2005. Male patient, 56 years of age, was diagnosed with hypertension, diabetes mellitus and was treated with Cozaar. After drug was administered, patient experienced the following side effects: nasopharyngitis, platelet count decreased. Cozaar dosage: unknown. During the same period patient was treated with BASEN, PREDONINE, COTRIM. Patient recovered.
Cozaar Side Effects Report #4590384-6
Cozaar side effect was reported by a Physician from on Feb 18, 2005. Female patient, 31 years of age, was diagnosed with glomerulonephritis proliferative and was treated with Cozaar. After drug was administered, patient experienced the following side effects: platelet count decreased, white blood cell count decreased. Cozaar dosage: unknown. Patient was hospitalized. Patient recovered.
Cozaar Side Effects Report #4600051-8
Cozaar side effect was reported by a Physician from on Feb 18, 2005. Female patient, 31 years of age, weighting 90.39 lb, was diagnosed with glomerulonephritis proliferative and was treated with Cozaar. After drug was administered, patient experienced the following side effects: platelet count decreased, white blood cell count decreased. Cozaar dosage: unknown. Patient was hospitalized. Patient recovered.
Cozaar Side Effects Report #4625575-9
Cozaar side effect was reported by a Physician from on Feb 18, 2005. Female patient, 31 years of age, weighting 90.39 lb, was diagnosed with glomerulonephritis proliferative and was treated with Cozaar. After drug was administered, patient experienced the following side effects: platelet count decreased, white blood cell count decreased. Cozaar dosage: unknown. Patient was hospitalized. Patient recovered.
Cozaar Side Effects Report #4640795-5
Cozaar side effect was reported by a Physician from on Feb 18, 2005. Female patient, 31 years of age, weighting 90.39 lb, was diagnosed with glomerulonephritis proliferative and was treated with Cozaar. After drug was administered, patient experienced the following side effects: platelet count decreased, white blood cell count decreased. Cozaar dosage: unknown. Patient was hospitalized. Patient recovered.
Cozaar Side Effects Report #4691339-3
Cozaar side effect was reported by a Physician from on May 26, 2005. Female patient, 74 years of age, weighting 116.8 lb, was diagnosed with essential hypertension, neoplasm prophylaxis, gastritis and was treated with Cozaar. After drug was administered, patient experienced the following side effects: cerebral haemorrhage, platelet count decreased. Cozaar dosage: unknown. During the same period patient was treated with GLYCYRON, TEPRENONE. Patient recovered.
Cozaar Side Effects Report #4591191-0
Cozaar side effect was reported by a Physician from on Feb 14, 2005. Female patient, 83 years of age, weighting 112.4 lb, was diagnosed with cardiac failure, atrial fibrillation
, thrombosis prophylaxis, hyperuricaemia and was treated with Cozaar. After drug was administered, patient experienced the following side effects: adverse event, cardiac failure, platelet count decreased. Cozaar dosage: unknown. During the same period patient was treated with ITOROL, FRANDOL TAPE S, DIGOXIN, PANALDINE, LASIX, ALLOPURINOL. Patient was hospitalized. Patient recovered.Cozaar Side Effects Report #4603796-9
Cozaar side effect was reported by a Physician from on Feb 14, 2005. Female patient, 83 years of age, weighting 112.4 lb, was diagnosed with cardiac failure, atrial fibrillation
, thrombosis prophylaxis, hyperuricaemia and was treated with Cozaar. After drug was administered, patient experienced the following side effects: adverse event, cardiac failure, platelet count decreased, refusal of treatment by patient. Cozaar dosage: unknown. During the same period patient was treated with ITOROL, FRANDOL TAPE S, DIGOXIN, PANALDINE, LASIX, ALLOPURINOL. Patient was hospitalized. Patient recovered.Cozaar Side Effects Report #5663590-7
Cozaar side effect was reported by a Consumer or non-health professional from BRAZIL on Dec 21, 2007. Female patient, 54 years of age, was diagnosed with cardiac failure and was treated with Cozaar. After drug was administered, patient experienced the following side effects: cardiogenic shock, haemodialysis, hepatic congestion, hypokalaemia, platelet count decreased, prothrombin time shortened, renal impairment, respiratory tract infection, septic shock. Cozaar dosage: unknown. During the same period patient was treated with AMIODARONE, DIGOXIN, FUROSEMIDE, LEVOTHYROXINE, PANTOPRAZOLE, SPIRONOLACTONE. Patient was hospitalized. Patient died.
Cozaar Side Effects Report #5748108-2
Cozaar side effect was reported by a Consumer or non-health professional from BRAZIL on Dec 21, 2007. Female patient, 54 years of age, was diagnosed with cardiac failure and was treated with Cozaar. After drug was administered, patient experienced the following side effects: asthenia, cardiogenic shock, haemodialysis, hepatic congestion, hypokalaemia, hypotension, platelet count decreased, prothrombin time shortened. Cozaar dosage: unknown. During the same period patient was treated with AMIODARONE, DIGOXIN, FUROSEMIDE, LEVOTHYROXINE, PANTOPRAZOLE, SPIRONOLACTONE. Patient was hospitalized. Patient died.
Cozaar Side Effects Report #5425107-1
Cozaar side effect was reported by a Physician from JAPAN on Aug 17, 2007. Female patient, 64 years of age, weighting 97.00 lb, was treated with Cozaar. After drug was administered, patient experienced the following side effects: blood creatine phosphokinase increased, hepatic function abnormal, pericarditis, platelet count decreased. Cozaar dosage: unknown. During the same period patient was treated with CILOSTAZOL, ADALAT, RENAGEL, CALTAN, PREDONINE. Patient was hospitalized. Patient recovered.
Cozaar Side Effects Report #5473176-5
Cozaar side effect was reported by a Physician from JAPAN on Sept 18, 2007. Female patient, 64 years of age, weighting 97.00 lb, was treated with Cozaar. After drug was administered, patient experienced the following side effects: blood creatine phosphokinase increased, hepatic function abnormal, pericarditis, platelet count decreased. Cozaar dosage: unknown. During the same period patient was treated with CILOSTAZOL, ADALAT, RENAGEL, CALTAN, PREDONINE. Patient was hospitalized. Patient recovered.
Cozaar Side Effects Report #4623919-5
Cozaar side effect was reported by a Pharmacist from on Mar 23, 2005. Female patient, 60 years of age, was treated with Cozaar. After drug was administered, patient experienced the following side effects: platelet count decreased. Cozaar dosage: unknown. During the same period patient was treated with RHEUMATREX, PREDNISOLONE. Patient recovered.
Cozaar Side Effects Report #5155264-6
Cozaar side effect was reported by a Physician from JAPAN on Oct 31, 2006. Female patient, 21 years of age, was treated with Cozaar. After drug was administered, patient experienced the following side effects: haemolytic anaemia, platelet count decreased. Cozaar dosage: unknown. During the same period patient was treated with ACTONEL, PERSANTINE, SUCRALFATE, PREDONINE. Patient was hospitalized. Patient recovered.
Cozaar Side Effects Report #5160148-3
Cozaar side effect was reported by a Physician from JAPAN on Oct 31, 2006. Female patient, 21 years of age, was treated with Cozaar. After drug was administered, patient experienced the following side effects: haemolytic anaemia, platelet count decreased. Cozaar dosage: unknown. During the same period patient was treated with ACTONEL, PERSANTIN, SUCRALFATE, PREDONINE. Patient was hospitalized. Patient recovered.
Cozaar Side Effects Report #5160154-9
Cozaar side effect was reported by a Physician from JAPAN on Oct 31, 2006. Female patient, 21 years of age, was treated with Cozaar. After drug was administered, patient experienced the following side effects: haemolytic anaemia, platelet count decreased. Cozaar dosage: unknown. During the same period patient was treated with ACTONEL, PERSANTINE, SUCRALFATE, PREDONINE. Patient was hospitalized. Patient recovered.
Cozaar Side Effects Report #5147305-7
Cozaar side effect was reported by a Physician from JAPAN on Oct 31, 2006. Female patient, 20 years of age, was treated with Cozaar. After drug was administered, patient experienced the following side effects: haemolytic anaemia, platelet count decreased. Cozaar dosage: unknown. Patient was hospitalized. Patient recovered.
Cozaar and platelet count decreased 