Actos and glycosylated haemoglobin increased Patient Reports February 09, 2010
Actos Side Effects Report #5838398-X
Actos side effect was reported by a Consumer or non-health professional from UNITED STATES on July 29, 2008. Female patient, 73 years of age, weighting 195.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with Actos. After drug was administered, patient experienced the following side effects: blood glucose increased, blood urea increased, fluid retention, gait disturbance, glycosylated haemoglobin increased, swelling, weight increased. Actos dosage: 15 MG, 1 IN 1 D, PER ORAL; 30 MG, 1 IN 1 D, PER ORAL. During the same period patient was treated with ASPIRIN, METOPROLOL TARTRATE, GEMFIBROZIL, LOVASTATIN, LISINOPRIL, FOLIC ACID, VITAMIN. Patient recovered.
Actos Side Effects Report #5909334-2
Actos side effect was reported by a Consumer or non-health professional from JAPAN on Sept 24, 2008. Male patient, 72 years of age, was diagnosed with type 2 diabetes mellitus and was treated with Actos. After drug was administered, patient experienced the following side effects: blood pressure increased, coronary artery occlusion, glycosylated haemoglobin increased, low density lipoprotein increased, myocardial infarction, weight decreased. Actos dosage: 30 MG (30 MG,1 IN 1 D) PER ORAL. During the same period patient was treated with GLUFAST, BASEN, BLOPRESS, CARVEDILOL, ASPIRIN, ZETIA, CRESTOR, AMARYL. Patient was hospitalized. Patient recovered.
Actos Side Effects Report #5727205-1
Actos side effect was reported by a Consumer or non-health professional from JAPAN on Apr 23, 2008. Male patient, 69 years of age, was diagnosed with type 2 diabetes mellitus and was treated with Actos. After drug was administered, patient experienced the following side effects: cardiac failure, glycosylated haemoglobin increased, oedema peripheral, parkinsonism, pneumonia bacterial, weight increased. Actos dosage: 15 MG (15 MG, 1 D) PER ORAL; 30 MG (30 MG, 1 IN 1 D) PER ORAL. During the same period patient was treated with CANDESARTAN CILEXETIL, SIMVASTATIN, ENALAPRIL MALEATE, GLYBURIDE, NIFEDIPINE, ALLOPURINOL, LASIX. Patient was hospitalized. Patient recovered.
Actos Side Effects Report #5761960-X
Actos side effect was reported by a Consumer or non-health professional from JAPAN on May 21, 2008. Male patient, 69 years of age, was diagnosed with type 2 diabetes mellitus and was treated with Actos. After drug was administered, patient experienced the following side effects: cardiac failure, dyspnoea, glycosylated haemoglobin increased, oedema peripheral, parkinsonism, pneumonia bacterial, weight increased. Actos dosage: 15 MG (15 MG, 1 D) PER ORAL; 30 MG (30 MG, 1 IN 1 D) PER ORAL. During the same period patient was treated with CANDESARTAN CILEXETIL, SIMVASTATIN, ENALAPRIL MALEATE, GLYBURIDE, ADALAT, ALLOPURINOL, LASIX. Patient was hospitalized. Patient recovered.
Actos Side Effects Report #5590626-4
Actos side effect was reported by a Consumer or non-health professional from UNITED STATES on Dec 28, 2007. Female patient, 65 years of age, weighting 204.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with Actos. After drug was administered, patient experienced the following side effects: breast cancer female, breast mass, glycosylated haemoglobin increased, pulmonary thrombosis, scar
. Actos dosage: 15 MG, 1 IN 1 D, PER ORAL : 30 MG, 1 IN 1 D, PER ORAL. During the same period patient was treated with GLUCOPHAGE, COUMADIN, ARIMIDEX. Patient was hospitalized. Patient recovered.Actos Side Effects Report #5732618-8
Actos side effect was reported by a Physician from UNITED STATES on Apr 25, 2008. Male patient, 65 years of age, weighting 220.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with Actos. After drug was administered, patient experienced the following side effects: arthralgia, blood glucose increased, glycosylated haemoglobin increased, malignant melanoma, meniscus lesion, precancerous skin lesion. Actos dosage: unknown. During the same period patient was treated with ACTOPLUS MET, ACTOPLUS MET, TAZTIA XT, AVALIDE, METFORMIN, PRAVACHOL. Patient recovered.
Actos Side Effects Report #5383621-1
Actos side effect was reported by a Consumer or non-health professional from JAPAN on June 26, 2007. Male patient, 60 years of age, was diagnosed with type 2 diabetes mellitus and was treated with Actos. After drug was administered, patient experienced the following side effects: dyspnoea, glycosylated haemoglobin increased, oedema peripheral, pulmonary oedema, rhinorrhoea, supraventricular extrasystoles, weight increased. Actos dosage: 15 MG (15 MG, 1 IN 1 D) PER ORAL. During the same period patient was treated with BLOPRESS, GLUFAST, AMARYL, LIVALO, NORVASC, SOLANTAL, FLOMOX. Patient recovered.
Actos Side Effects Report #5869663-8
Actos side effect was reported by a Consumer or non-health professional from JAPAN on Aug 20, 2008. Female patient, 55 years of age, was diagnosed with type 2 diabetes mellitus and was treated with Actos. After drug was administered, patient experienced the following side effects: acute pulmonary oedema, atrial fibrillation
, blood pressure increased, brain natriuretic peptide increased, chest discomfort, dyspnoea, glycosylated haemoglobin increased, oxygen saturation decreased. Actos dosage: 15 MG (15 MG, 1 IN 1 D) PER ORAL. During the same period patient was treated with BASEN OD, NOVORAPID, DIOVAN, BISOPROLOL FUMARATE, LOXONIN, KAKKON. Patient was hospitalized. Patient recovered.Actos Side Effects Report #5944512-8
Actos side effect was reported by a Consumer or non-health professional from JAPAN on Oct 28, 2008. Female patient, 55 years of age, was diagnosed with type 2 diabetes mellitus and was treated with Actos. After drug was administered, patient experienced the following side effects: ascites, blood glucose increased, glycosylated haemoglobin increased, oedema peripheral, pericardial effusion, pleural effusion, snoring
. Actos dosage: 15 MG (15 MG, 1 IN 1 D) PER ORAL. During the same period patient was treated with AMARYL, GLUCOBAY, LUPRAC, MICARDIS, NORVASC, GASMOTIN. Patient was hospitalized. Patient recovered.Actos Side Effects Report #6060411-8
Actos side effect was reported by a Health Professional from UNITED STATES on Jan 29, 2009. Female patient, 54 years of age, weighting 210.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with Actos. After drug was administered, patient experienced the following side effects: arthralgia, blood glucose increased, fatigue, glycosylated haemoglobin increased, ill-defined disorder, vitamin d deficiency, weight increased. Actos dosage: 15MG TID PO. During the same period patient was treated with VITAMIN D. Patient recovered.
Actos Side Effects Report #5613172-8
Actos side effect was reported by a Consumer or non-health professional from FRANCE on Jan 22, 2008. Female patient, 73 years of age, was diagnosed with type 1 diabetes mellitus and was treated with Actos. After drug was administered, patient experienced the following side effects: glycosylated haemoglobin increased, weight increased. Actos dosage: 15 MG (15 MG, 1 IN 1 D) ORAL. During the same period patient was treated with INSULIN, COAPROVEL, ALDACTONE, PLAVIX. Patient died.
Actos Side Effects Report #5242197-X
Actos side effect was reported by a Consumer or non-health professional from JAPAN on Jan 31, 2007. Male patient, 81 years of age, was diagnosed with insulin-requiring type ii diabetes mellitus and was treated with Actos. After drug was administered, patient experienced the following side effects: diabetes mellitus inadequate control, glycosylated haemoglobin increased, nasopharyngitis, platelet count decreased, white blood cell count decreased. Actos dosage: unknown. During the same period patient was treated with AMARYL. Patient recovered.
Actos Side Effects Report #5266698-3
Actos side effect was reported by a Consumer or non-health professional from JAPAN on Feb 27, 2007. Male patient, 54 years of age, was diagnosed with insulin-requiring type ii diabetes mellitus, hypercholesterolaemia, demyelinating polyneuropathy and was treated with Actos. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, blood lactate dehydrogenase increased, diabetes mellitus inadequate control, gamma-glutamyltransferase increased, glycosylated haemoglobin increased. Actos dosage: unknown. During the same period patient was treated with LIPITOR, CORTICOSTEROIDS, IMURAN, NOVORAPID. Patient was hospitalized. Patient recovered.
Actos Side Effects Report #4568436-6
Actos side effect was reported by a Consumer or non-health professional from on Jan 25, 2005. Female patient, 68 years of age, was diagnosed with insulin resistant diabetes and was treated with Actos. After drug was administered, patient experienced the following side effects: blood glucose increased, glycosylated haemoglobin increased, hyperkalaemia. Actos dosage: 15 MG (15 MG, 1 IN 1 D) PER ORAL. During the same period patient was treated with DIOVAN, GLYBURIDE, DIGITOXIN. Patient recovered.
Actos Side Effects Report #5169537-4
Actos side effect was reported by a Physician from UNITED STATES on Nov 21, 2006. Male patient, 82 years of age, weighting 179.0 lb, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actos. After drug was administered, patient experienced the following side effects: dialysis
, dyspnoea, ejection fraction decreased, glomerulosclerosis, glycosylated haemoglobin increased, rales, weight increased. Actos dosage: 30 MG, 1 IN 1 D, PER ORAL. During the same period patient was treated with INSULIN GLARGINE, NIACIN, VITAMIN B, ZETIA. Patient was hospitalized. Patient recovered.Actos Side Effects Report #4664709-7
Actos side effect was reported by a Consumer or non-health professional from on Sept 19, 2003. Male patient, 79 years of age, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actos. After drug was administered, patient experienced the following side effects: atrial fibrillation
, back pain
, blood glucose increased, cardiac failure acute, cardiac fibrillation, cardiomegaly, decreased appetite, glycosylated haemoglobin increased, heart rate increased. Actos dosage: 15 MG(15 MG, 1 IN 1 D), PER ORAL. During the same period patient was treated with BLOPRESSELTS, BASEN, GLYBURIDE, ATELEC. Patient was hospitalized. Patient died.Actos Side Effects Report #4745325-5
Actos side effect was reported by a Consumer or non-health professional from GERMANY on Aug 16, 2005. Female patient, 76 years of age, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actos. After drug was administered, patient experienced the following side effects: abdominal pain upper, anorexia, back pain
, condition aggravated, cyanosis, depression
, dry mouth, glycosylated haemoglobin increased, hepatitis
. Actos dosage: 30 MG (30 MCI, 1 IN 1 D), PER ORAL. During the same period patient was treated with RANITIDINE. Patient was hospitalized. Patient recovered.Actos Side Effects Report #4909809-9
Actos side effect was reported by a Physician from UNITED STATES on Jan 30, 2006. Female patient, 76 years of age, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actos. After drug was administered, patient experienced the following side effects: anaemia, blood glucose increased, cardiac murmur, cerebral cyst, cerebral ventricle dilatation, depressed level of consciousness, feeling abnormal, glycosylated haemoglobin increased, haematoma. Actos dosage: unknown. During the same period patient was treated with BYETTA, AMARYL, ASPIRIN, CARVEDILOL, ATORVASTATIN CALCIUM, LISINOPRIL, SERTRALINE. Patient was hospitalized. Patient recovered.
Actos Side Effects Report #5291087-5
Actos side effect was reported by a Consumer or non-health professional from JAPAN on Mar 20, 2007. Male patient, 74 years of age, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actos. After drug was administered, patient experienced the following side effects: colonic polyp
, diarrhoea, gallbladder disorder, gastric cancer, gastric ulcer, gastritis, glycosylated haemoglobin increased, hepatic steatosis, nasopharyngitis. Actos dosage: 30 MG (30 MG, 1 IN 1 D), PER ORAL. During the same period patient was treated with NATEGLINIDE, AMARYL, KINEDAK. Patient recovered.Actos Side Effects Report #4662038-9
Actos side effect was reported by a Physician from on May 04, 2005. Female patient, 74 years of age, weighting 182.0 lb, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actos. After drug was administered, patient experienced the following side effects: blood albumin increased, glycosylated haemoglobin increased, myocardial infarction, pain
, pain in extremity. Actos dosage: 15 MG, 1 IN 1 D, PER ORAL. During the same period patient was treated with CRESTOR, FUROSEMIDE. Patient was hospitalized. Patient recovered.Actos Side Effects Report #5312941-1
Actos side effect was reported by a Health Professional from UNITED STATES on Apr 13, 2007. Female patient, 72 years of age, weighting 142.0 lb, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actos. After drug was administered, patient experienced the following side effects: glycosylated haemoglobin increased, retinal oedema, weight increased. Actos dosage: 30 MG, 1 IN 1 D, PER ORAL. During the same period patient was treated with ARMOUR THYROID. Patient recovered.
Actos Side Effects Report #5318540-X
Actos side effect was reported by a Health Professional from UNITED STATES on Apr 19, 2007. Female patient, 72 years of age, weighting 142.0 lb, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actos. After drug was administered, patient experienced the following side effects: glycosylated haemoglobin increased, retinal oedema, weight increased. Actos dosage: 30 MG, 1 IN 1 D, PER ORAL. During the same period patient was treated with ARMOUR THYROID. Patient recovered.
Actos Side Effects Report #4954424-4
Actos side effect was reported by a Consumer or non-health professional from JAPAN on Mar 10, 2006. Male patient, 71 years of age, was diagnosed with diabetes mellitus non-insulin-dependent, hypertension, myocardial ischaemia and was treated with Actos. After drug was administered, patient experienced the following side effects: atrioventricular block complete, atrioventricular block second degree, glycosylated haemoglobin increased, treatment noncompliance. Actos dosage: 15 MG (15 MG, 1 IN 1 D) PER ORAL. During the same period patient was treated with DILTIAZEM, NICORANDIS, ASPIRIN, ISOSORBIDE DINITRATE, ALLOPURINOL, GLYBURIDE, GLUCOBAY. Patient recovered.
Actos Side Effects Report #4767788-1
Actos side effect was reported by a Consumer or non-health professional from JAPAN on Sept 06, 2005. Female patient, 70 years of age, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actos. After drug was administered, patient experienced the following side effects: acute myocardial infarction, blood creatinine decreased, blood glucose increased, brain natriuretic peptide increased, coronary artery occlusion, dehydration, gamma-glutamyltransferase increased, glycosylated haemoglobin increased, haematocrit increased. Actos dosage: 15 MG (15 MG, 1 IN 1 D) PER ORAL. Patient was hospitalized. Patient recovered.
Actos Side Effects Report #4869584-3
Actos side effect was reported by a Consumer or non-health professional from JAPAN on Dec 19, 2005. Female patient, 70 years of age, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actos. After drug was administered, patient experienced the following side effects: acute myocardial infarction, blood alkaline phosphatase increased, blood creatinine decreased, gamma-glutamyltransferase increased, glycosylated haemoglobin increased, haematocrit increased, neck pain, rash vesicular, red blood cell count increased. Actos dosage: unknown. Patient was hospitalized. Patient recovered.
Actos Side Effects Report #4869589-2
Actos side effect was reported by a Consumer or non-health professional from JAPAN on Dec 19, 2005. Female patient, 70 years of age, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actos. After drug was administered, patient experienced the following side effects: acute myocardial infarction, blood alkaline phosphatase increased, blood creatinine decreased, coronary artery occlusion, gamma-glutamyltransferase increased, glycosylated haemoglobin increased, haematocrit increased, heart rate increased, hypothyroidism. Actos dosage: unknown. Patient was hospitalized. Patient recovered.
Actos Side Effects Report #4889478-7
Actos side effect was reported by a Physician from JAPAN on Jan 16, 2006. Female patient, 70 years of age, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actos. After drug was administered, patient experienced the following side effects: acute myocardial infarction, blood alkaline phosphatase increased, blood creatinine decreased, coronary artery occlusion, gamma-glutamyltransferase increased, glycosylated haemoglobin increased, haematocrit increased, hypothyroidism, liver disorder. Actos dosage: unknown. Patient was hospitalized. Patient recovered.
Actos Side Effects Report #4915891-5
Actos side effect was reported by a Consumer or non-health professional from UNITED STATES on Feb 07, 2006. Female patient, 70 years of age, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actos. After drug was administered, patient experienced the following side effects: acute myocardial infarction, blood creatinine decreased, brain natriuretic peptide increased, coronary artery occlusion, gamma-glutamyltransferase increased, glycosylated haemoglobin increased, haematocrit increased, neck pain, rash
. Actos dosage: unknown. Patient was hospitalized. Patient recovered.Actos Side Effects Report #5148315-6
Actos side effect was reported by a Consumer or non-health professional from FRANCE on Oct 27, 2006. Female patient, 69 years of age, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actos. After drug was administered, patient experienced the following side effects: glycosylated haemoglobin increased, macular oedema, retinal aneurysm. Actos dosage: 30 MG (30 MG, 1 IN 1 D) ORAL. During the same period patient was treated with DIAMICRON, GLUCOPHAGE, ATORVASTATIN CALCIUM, COTAREG, CELECTOL, ASPEGIC. Patient recovered.
Actos Side Effects Report #4903519-X
Actos side effect was reported by a Consumer or non-health professional from JAPAN on Jan 25, 2006. Male patient, 69 years of age, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actos. After drug was administered, patient experienced the following side effects: blood glucose increased, glycosylated haemoglobin increased, prostate cancer
, rhinorrhoea, sneezing. Actos dosage: 30 MG (30 MG, 1 D) PER ORAL. During the same period patient was treated with NATEGLINIDE, AMLODIPINE BESYLATE, LOSARTAN POTASSIUM, OMEPRAZOLE, SELBEX, LAMISIL. Patient was hospitalized. Patient recovered.Actos Side Effects Report #4991423-0
Actos side effect was reported by a Consumer or non-health professional from JAPAN on Apr 25, 2006. Male patient, 68 years of age, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actos. After drug was administered, patient experienced the following side effects: blood glucose increased, glycosylated haemoglobin increased, prostate cancer
, rhinorrhoea, sneezing. Actos dosage: 30 MG (30 MG 1 IN 1/D) PER ORAL. During the same period patient was treated with NATEGLINIDE, AMLODIPINE BESYLATE, LOSARTAN POTASSIUM, OMEPRAZOLE, SELBEX, LAMISIL. Patient was hospitalized. Patient recovered.Actos Side Effects Report #5201863-2
Actos side effect was reported by a Consumer or non-health professional from AUSTRIA on Dec 19, 2006. Male patient, 67 years of age, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actos. After drug was administered, patient experienced the following side effects: cervicobrachial syndrome, dental caries, diabetic microangiopathy, diplopia, fatigue, glycosylated haemoglobin increased, headache
, hyperlipidaemia. Actos dosage: 30 MG (30 MG, 1 IN 1 D) PER ORAL. During the same period patient was treated with TENORMIN, GLUCOPHAGE, ALLOPURINOL. Patient was hospitalized. Patient recovered.Actos Side Effects Report #5313747-X
Actos side effect was reported by a Consumer or non-health professional from AUSTRIA on Apr 17, 2007. Male patient, 63 years of age, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actos. After drug was administered, patient experienced the following side effects: cardiac failure, coronary arterial stent insertion, glycosylated haemoglobin increased, pulmonary oedema. Actos dosage: 45 MG (45 MG, 1 IN 1 D) PER ORAL. During the same period patient was treated with DIABETEX, COSAAR PLUS, CARVEDILOL, LESCOL MR, SPIRIVA, PLAVIX, FURON, GLIMEPIRIDE. Patient was hospitalized. Patient recovered.
Actos Side Effects Report #5128718-6
Actos side effect was reported by a Consumer or non-health professional from UNITED STATES on Sept 27, 2006. Female patient, 62 years of age, weighting 157.0 lb, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actos. After drug was administered, patient experienced the following side effects: blood glucose increased, feeling abnormal, glare, glycosylated haemoglobin increased, photophobia, toothache, treatment noncompliance, visual disturbance. Actos dosage: unknown. During the same period patient was treated with HYZAAR, NORVASC, CILOSTAZOL, NEXIUM. Patient recovered.
Actos Side Effects Report #5340032-2
Actos side effect was reported by a Consumer or non-health professional from KOREA, REPUBLIC OF on May 22, 2007. Male patient, 61 years of age, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actos. After drug was administered, patient experienced the following side effects: blood creatinine increased, condition aggravated, diabetes mellitus, glycosylated haemoglobin increased, haematocrit decreased, haemoglobin decreased, hypertension, oedema. Actos dosage: 15 MG (15 MG, 1 IN 1 D) PER ORAL. During the same period patient was treated with NPH INSULIN, MONOPRIL, AMLODIPINE BESYLATE, ADALAT, CARVEDILOL, ZAROXOLYN, FUROSEMIDE, THIOCTACID. Patient was hospitalized. Patient recovered.
Actos Side Effects Report #5118901-8
Actos side effect was reported by a Consumer or non-health professional from JAPAN on Sept 15, 2006. Male patient, 60 years of age, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actos. After drug was administered, patient experienced the following side effects: blood alkaline phosphatase increased, blood glucose increased, condition aggravated, gamma-glutamyltransferase increased, glycosylated haemoglobin increased, no therapeutic response, pancreatic duct dilatation, thirst. Actos dosage: unknown. During the same period patient was treated with GLUCOBAY, URSO, LANTUS. Patient recovered.
Actos Side Effects Report #5354819-3
Actos side effect was reported by a Consumer or non-health professional from UNITED STATES on May 29, 2007. Male patient, 58 years of age, weighting 184.0 lb, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actos. After drug was administered, patient experienced the following side effects: blood glucose decreased, disease recurrence, glycosylated haemoglobin increased, hepatitis c
, insomnia, tremor. Actos dosage: 15 MG, 1 IN 1 D, PER ORAL. During the same period patient was treated with GLYBURIDE, LISINOPRIL, RIBAVIRIN INTERFERON. Patient recovered.Actos Side Effects Report #5167273-1
Actos side effect was reported by a Consumer or non-health professional from JAPAN on Nov 16, 2006. Male patient, 55 years of age, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actos. After drug was administered, patient experienced the following side effects: autoimmune hepatitis, blood lactate dehydrogenase increased, diarrhoea, glycosylated haemoglobin increased, haemorrhagic diathesis, headache
, hepatic necrosis, hepatitis b
, liver disorder. Actos dosage: 30 MG (30 MG, 1 IN 1 D) PER ORAL. During the same period patient was treated with BASEN, AMARYL, METFORMIN. Patient was hospitalized. Patient recovered.Actos Side Effects Report #5314650-1
Actos side effect was reported by a Physician from JAPAN on Apr 16, 2007. Male patient, 54 years of age, was diagnosed with diabetes mellitus non-insulin-dependent, chronic inflammatory demyelinating polyradiculoneuropathy, hypercholesterolaemia and was treated with Actos. After drug was administered, patient experienced the following side effects: cholangitis, chronic inflammatory demyelinating polyradiculoneuropathy, computerised tomogram abnormal, diabetes mellitus inadequate control, gastric disorder, glycosylated haemoglobin increased, hepatic cyst, hepatic necrosis, hepatocellular damage. Actos dosage: unknown. During the same period patient was treated with IMURAN, LIPITOR, PREDNISOLONE, NOVORAPID. Patient was hospitalized. Patient recovered.
Actos Side Effects Report #4653925-6
Actos side effect was reported by a Consumer or non-health professional from on Apr 22, 2005. Male patient, 46 years of age, was diagnosed with diabetes mellitus non-insulin-dependent, hiv infection
and was treated with Actos. After drug was administered, patient experienced the following side effects: blood cholesterol increased, blood triglycerides increased, glycosylated haemoglobin increased, myocardial infarction. Actos dosage: unknown. During the same period patient was treated with DIAMICRON, MEDIATOR, VIRAMUNE, COMBIVIR. Patient was hospitalized. Patient recovered.Actos Side Effects Report #5141019-5
Actos side effect was reported by a Consumer or non-health professional from JAPAN on Oct 13, 2006. Male patient, 42 years of age, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actos. After drug was administered, patient experienced the following side effects: condition aggravated, glycosylated haemoglobin increased, macular oedema. Actos dosage: 30 MG (30 MG, 1 IN 1 D), PER ORAL. During the same period patient was treated with AMARYL, GLUCOBAY, TICLOPIDINE, LOCHOL, GASMOTIN. Patient recovered.
Actos Side Effects Report #5197712-1
Actos side effect was reported by a Consumer or non-health professional from JAPAN on Dec 14, 2006. Male patient, 42 years of age, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actos. After drug was administered, patient experienced the following side effects: glycosylated haemoglobin increased, macular oedema. Actos dosage: 30 MG (30 MG, 1 IN 1 D), PER ORAL. During the same period patient was treated with AMARYL, GLUCOBAY, TICLOPIDINE, LOCHOL, GASMOTIN. Patient recovered.
Actos Side Effects Report #5004174-3
Actos side effect was reported by a Physician from UNITED STATES on May 03, 2006. Male patient, 42 years of age, weighting 250.0 lb, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actos. After drug was administered, patient experienced the following side effects: anxiety
, blood glucose increased, glycosylated haemoglobin increased, haemoglobin decreased, myocardial infarction, visual disturbance. Actos dosage: 30 MG, 1 IN 1 D, PER ORAL. During the same period patient was treated with GLUCOVANCE, INSULIN, LANTUS, TOPROL, VICOPROFEN, FLEXERIL, NEXIUM, LIPITOR. Patient was hospitalized. Patient recovered.Actos Side Effects Report #4661081-3
Actos side effect was reported by a Consumer or non-health professional from on May 02, 2005. Female patient, 25 years of age, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actos. After drug was administered, patient experienced the following side effects: caesarean section, diabetes mellitus inadequate control, foetal growth retardation, glycosylated haemoglobin increased, hypersensitivity, placental insufficiency, pregnancy
, pregnancy induced hypertension. Actos dosage: 45 MG (45 MG, 1 IN 1 D) PER ORAL. During the same period patient was treated with METFORMIN HYDROCHLORIDE, BISOPROLOL, LEVOTHYROXINE. Patient was hospitalized. Patient recovered.Actos Side Effects Report #4573023-X
Actos side effect was reported by a Physician from on Jan 26, 2005. Male patient was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actos. After drug was administered, patient experienced the following side effects: glycosylated haemoglobin increased, weight decreased. Actos dosage: 30 MG (30 MG, 1 IN 1 D), ORAL. Patient was hospitalized. Patient recovered.
Actos Side Effects Report #4896849-1
Actos side effect was reported by a Health Professional from JAPAN on Jan 20, 2006. Male patient was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actos. After drug was administered, patient experienced the following side effects: blood glucose increased, glycosylated haemoglobin increased. Actos dosage: 30 MG PER (30MG.1 D). During the same period patient was treated with NATEGLINIDE. Patient was hospitalized. Patient recovered.
Actos Side Effects Report #5465555-7
Actos side effect was reported by a Consumer or non-health professional from JAPAN on Sept 12, 2007. Female patient, 83 years of age, was diagnosed with diabetes mellitus and was treated with Actos. After drug was administered, patient experienced the following side effects: anaphylactic shock, blood glucose increased, chest discomfort, dizziness
, dyspnoea, glycosylated haemoglobin increased, immobile, pruritus genital, swelling. Actos dosage: 15MG (15 MG, 1 -2), PER ORAL; 15 MG (15 MG, 1 IN 1 D); 30 MG (30 MG, 1 IN 1 D) PER ORAL. During the same period patient was treated with BASEN OD, NATEGLINIDE, COLCHICUM JTL LIQ, ALFAROL, ASPARA. Patient was hospitalized. Patient recovered.Actos Side Effects Report #5090684-X
Actos side effect was reported by a Consumer or non-health professional from JAPAN on Aug 09, 2006. Female patient, 78 years of age, was diagnosed with diabetes mellitus and was treated with Actos. After drug was administered, patient experienced the following side effects: computerised tomogram thorax abnormal, cough, cyanosis, dyspnoea, glycosylated haemoglobin increased, interstitial lung disease, lymphocyte count increased, malaise, pco2 increased. Actos dosage: 15 MG (15 MG, 1 IN 1 D) PER ORAL. During the same period patient was treated with BASEN OD, GLYBURIDE, COMELIAN, DILTIAZEM HYDROCHLORIDE, ENALAPRIL MALEATE, LENDORM. Patient was hospitalized. Patient recovered.
Actos Side Effects Report #5383022-6
Actos side effect was reported by a Consumer or non-health professional from JAPAN on June 22, 2007. Female patient, 78 years of age, was diagnosed with diabetes mellitus and was treated with Actos. After drug was administered, patient experienced the following side effects: colitis ulcerative, gastrointestinal erosion, glycosylated haemoglobin increased, hypoglycaemia. Actos dosage: 15 MG (15 MG, 1 IN 1 D) PER ORAL. During the same period patient was treated with EPINASTINE HYDROCHLORIDE, NILDILART, GOODMIN, NOVORAPID, HUMACART. Patient was hospitalized. Patient recovered.
Actos Side Effects Report #5372875-3
Actos side effect was reported by a Consumer or non-health professional from JAPAN on June 12, 2007. Male patient, 74 years of age, was diagnosed with diabetes mellitus and was treated with Actos. After drug was administered, patient experienced the following side effects: depressed level of consciousness, fall
, glycosylated haemoglobin increased, rhabdomyolysis, urinary incontinence
. Actos dosage: unknown. During the same period patient was treated with AMLODIPINE BESYLATE, GLYBURIDE. Patient was hospitalized. Patient recovered.Actos Side Effects Report #5388690-0
Actos side effect was reported by a Consumer or non-health professional from JAPAN on June 30, 2007. Female patient, 73 years of age, was diagnosed with diabetes mellitus, senile dementia and was treated with Actos. After drug was administered, patient experienced the following side effects: abasia, anorexia, arrhythmia
, asthenia, back pain
, blood creatine phosphokinase increased, cerebral infarction, glycosylated haemoglobin increased, hemiparesis. Actos dosage: 15 MG (15 MG, 1 IN 1 D), PER ORAL. During the same period patient was treated with ARICEPT, METRION, NATEGLINIDE, SAWACHION S, LEPRINTON. Patient recovered.Actos Side Effects Report #4911206-7
Actos side effect was reported by a Consumer or non-health professional from JAPAN on Jan 27, 2006. Male patient, 71 years of age, was diagnosed with diabetes mellitus and was treated with Actos. After drug was administered, patient experienced the following side effects: abasia, asthenia, blood glucose increased, cerebral atrophy, glycosylated haemoglobin increased, hypoaesthesia, myocardial infarction, rhabdomyolysis, viral infection
. Actos dosage: 15 MG (15 MG, 1 IN 1 D), PER ORAL. During the same period patient was treated with NORVASC, LOSARTAN POTASSIUM, ALMATOL, GLYBURIDE. Patient was hospitalized. Patient recovered.Actos Side Effects Report #4932632-6
Actos side effect was reported by a Physician from JAPAN on Feb 16, 2006. Male patient, 71 years of age, was diagnosed with diabetes mellitus and was treated with Actos. After drug was administered, patient experienced the following side effects: blood glucose increased, cerebral atrophy, glycosylated haemoglobin increased, hypertension, hypoaesthesia, rhabdomyolysis. Actos dosage: 15 MG (15 MG, 1 IN 1 D) PER ORAL. During the same period patient was treated with NORVASC, LOSARTAN POTASSIUM, ALMATOL, GLYBURIDE. Patient was hospitalized. Patient recovered.
Actos Side Effects Report #4976165-X
Actos side effect was reported by a Consumer or non-health professional from JAPAN on Mar 30, 2006. Male patient, 70 years of age, was diagnosed with diabetes mellitus and was treated with Actos. After drug was administered, patient experienced the following side effects: cholecystitis, cholelithiasis, diabetes mellitus inadequate control, glycosylated haemoglobin increased, lymphocyte percentage decreased, pyrexia, renal impairment, rhabdomyolysis, sepsis
. Actos dosage: unknown. During the same period patient was treated with EUGLUCON, METFORMIN. Patient was hospitalized. Patient recovered.Actos Side Effects Report #5362862-3
Actos side effect was reported by a Consumer or non-health professional from KOREA, REPUBLIC OF on June 08, 2007. Female patient, 66 years of age, was diagnosed with diabetes mellitus and was treated with Actos. After drug was administered, patient experienced the following side effects: blood cholesterol increased, blood glucose increased, glycosylated haemoglobin increased, hepatic neoplasm malignant. Actos dosage: 15 MG PER ORAL. During the same period patient was treated with AMARYL. Patient died.
Actos Side Effects Report #5368530-6
Actos side effect was reported by a Physician from KOREA, REPUBLIC OF on June 14, 2007. Female patient, 66 years of age, was diagnosed with diabetes mellitus and was treated with Actos. After drug was administered, patient experienced the following side effects: blood glucose increased, glycosylated haemoglobin increased, hepatic neoplasm malignant. Actos dosage: 15 MG PER ORAL. During the same period patient was treated with AMARYL. Patient died.
Actos Side Effects Report #5372666-3
Actos side effect was reported by a Consumer or non-health professional from KOREA, REPUBLIC OF on June 20, 2007. Female patient, 66 years of age, was diagnosed with diabetes mellitus and was treated with Actos. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood cholesterol increased, glycosylated haemoglobin increased, hepatic neoplasm malignant. Actos dosage: 15 MG. During the same period patient was treated with AMARYL. Patient died.
Actos Side Effects Report #5305726-3
Actos side effect was reported by a Consumer or non-health professional from AUSTRIA on Apr 06, 2007. Male patient, 63 years of age, was diagnosed with diabetes mellitus and was treated with Actos. After drug was administered, patient experienced the following side effects: cardiac failure, glycosylated haemoglobin increased, pulmonary oedema. Actos dosage: unknown. Patient was hospitalized. Patient recovered.
Actos Side Effects Report #5022079-9
Actos side effect was reported by a Consumer or non-health professional from JAPAN on May 25, 2006. Male patient, 61 years of age, was diagnosed with diabetes mellitus and was treated with Actos. After drug was administered, patient experienced the following side effects: blood glucose increased, cerebrovascular disorder, depressed level of consciousness, electroencephalogram abnormal, glycosylated haemoglobin increased, hyperammonaemia, metastases to liver, refusal of treatment by patient. Actos dosage: unknown. During the same period patient was treated with BASEN, AMARYL, URSO, KELNAC, EXCELASE. Patient was hospitalized. Patient recovered.
Actos Side Effects Report #5219244-4
Actos side effect was reported by a Consumer or non-health professional from JAPAN on Jan 10, 2007. Female patient, 51 years of age, was diagnosed with diabetes mellitus and was treated with Actos. After drug was administered, patient experienced the following side effects: glycosylated haemoglobin increased, macular oedema, oedema peripheral, visual disturbance, weight increased. Actos dosage: unknown. During the same period patient was treated with GLYBURIDE. Patient recovered.
Actos Side Effects Report #5472450-6
Actos side effect was reported by a Consumer or non-health professional from JAPAN on Sept 13, 2007. Female patient, 51 years of age, was diagnosed with diabetes mellitus and was treated with Actos. After drug was administered, patient experienced the following side effects: blood glucose increased, glycosylated haemoglobin increased, macular oedema, oedema peripheral, retinopathy, scotoma, visual acuity reduced, weight fluctuation. Actos dosage: 30 MG (30 MG, 1 D) PER ORAL; 15 MG (15 MG, 1 IN 1 D) PER ORAL. During the same period patient was treated with GLYBURIDE. Patient recovered.
Actos Side Effects Report #5293606-1
Actos side effect was reported by a Consumer or non-health professional from GERMANY on Mar 22, 2007. Male patient was diagnosed with diabetes mellitus and was treated with Actos. After drug was administered, patient experienced the following side effects: bundle branch block left, cardiac failure, cholelithiasis, condition aggravated, glycosylated haemoglobin increased, renal failure, respiratory failure, sleep apnoea syndrome, ventricular extrasystoles. Actos dosage: 45 MG. During the same period patient was treated with METFORMIN, DIURETICS, BETA BLOCKING AGENTS, RENIN, ANTITHROMBOTIC AGENTS. Patient was hospitalized. Patient recovered.
Actos Side Effects Report #4764626-8
Actos side effect was reported by a Physician from UNITED STATES on Aug 25, 2005. Male patient, weighting 268.0 lb, was diagnosed with diabetes mellitus and was treated with Actos. After drug was administered, patient experienced the following side effects: glycosylated haemoglobin increased, pancreatitis acute. Actos dosage: unknown. During the same period patient was treated with BYETTA, GLUCOPHAGE, HUMULIN N. Patient was hospitalized. Patient recovered.
Actos Side Effects Report #4833723-0
Actos side effect was reported by a Physician from UNITED STATES on Nov 03, 2005. Male patient, weighting 268.0 lb, was diagnosed with diabetes mellitus and was treated with Actos. After drug was administered, patient experienced the following side effects: blood lactic acid increased, glycosylated haemoglobin increased, pancreatitis acute. Actos dosage: unknown. During the same period patient was treated with BYETTA, GLUCOPHAGE, HUMULIN NPH. Patient was hospitalized. Patient recovered.
Actos Side Effects Report #4653054-1
Actos side effect was reported by a Health Professional from on Apr 22, 2005. Female patient, 68 years of age, weighting 180.0 lb, was diagnosed with blood glucose increased and was treated with Actos. After drug was administered, patient experienced the following side effects: blood glucose increased, glycosylated haemoglobin increased. Actos dosage: unknown. During the same period patient was treated with GLUCOTROL, SYNTHROID, IBUPROFEN, LIPITOR. Patient recovered.
Actos Side Effects Report #4643005-8
Actos side effect was reported by a Health Professional from on Apr 06, 2005. Female patient, 68 years of age, weighting 180.0 lb, was treated with Actos. After drug was administered, patient experienced the following side effects: blood glucose increased, glycosylated haemoglobin increased. Actos dosage: 15 MG, 1 IN 1 D, PER ORAL. During the same period patient was treated with GLUCOTROL, SYNTHROID, IBUPROFEN, LIPITOR. Patient recovered.
Actos Side Effects Report #4657458-2
Actos side effect was reported by a Health Professional from on Apr 22, 2005. Female patient, 68 years of age, weighting 180.0 lb, was treated with Actos. After drug was administered, patient experienced the following side effects: blood glucose increased, glycosylated haemoglobin increased, treatment noncompliance. Actos dosage: unknown. During the same period patient was treated with GLUCOTROL, SYNTHROID, IBUPROFEN, LIPITOR. Patient recovered.
Actos Side Effects Report #5625153-9
Actos side effect was reported by a Consumer or non-health professional from IRELAND on Jan 28, 2008. Male patient, 65 years of age, was treated with Actos. After drug was administered, patient experienced the following side effects: blood glucose increased, dysstasia, eye rolling, glycosylated haemoglobin increased. Actos dosage: unknown. During the same period patient was treated with GLUCOPHAGE, DIAMICRON. Patient recovered.
Actos Side Effects Report #4784282-2
Actos side effect was reported by a Physician from UNITED STATES on Sept 19, 2005. Female patient was treated with Actos. After drug was administered, patient experienced the following side effects: blood glucose increased, cholecystitis acute, glycosylated haemoglobin increased, nausea
, weight decreased. Actos dosage: unknown. During the same period patient was treated with EXENATIDE, GLUCOPHAGE. Patient was hospitalized. Patient recovered.Actos Side Effects Report #4832601-0
Actos side effect was reported by a Physician from UNITED STATES on Nov 09, 2005. Female patient was treated with Actos. After drug was administered, patient experienced the following side effects: cholecystitis acute, disease recurrence, glycosylated haemoglobin increased, weight decreased. Actos dosage: unknown. During the same period patient was treated with EXENATIDE, GLUCOPHAGE. Patient was hospitalized. Patient recovered.
Actos and glycosylated haemoglobin increased 