Takepron Side Effects
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Recently reported Takepron Side Effects
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Takepron Side Effects reported on Patientsville.com
None reported at this time.Takepron Side Effects reported to FDA
Takepron Side Effects Report #5213217-3
Physician from JAPAN reported Takepron side effect on Sept 12, 2006. Male patient, 70 years of age, was diagnosed with reflux oesophagitis and was treated with Takepron. After drug was administered, patient experienced the following side effects: oculomucocutaneous syndrome. Takepron dosage: unknown. During the same period patient was treated with LASIX, LOXONIN. Patient was hospitalized. Patient recovered.
Takepron Side Effects Report #5223675-6
Takepron side effect was reported by a Consumer or non-health professional from JAPAN on Jan 23, 2007. Male patient, 75 years of age, was diagnosed with gastric ulcer haemorrhage and was treated with Takepron. After drug was administered, patient experienced the following side effects: haematemesis, pyrexia, renal failure acute, shock. Takepron dosage: 30 MG PER ORAL. During the same period patient was treated with OMEPRAZOLE, SIGMART, PREDNISOLONE, HALCION, MUCOSTA. Patient recovered.
Takepron Side Effects Report #5269674-X
Consumer or non-health professional from JAPAN reported Takepron side effect on Mar 09, 2007. Female patient, 68 years of age, was diagnosed with reflux oesophagitis and was treated with Takepron. After drug was administered, patient experienced the following side effects: blood creatine phosphokinase increased, myalgia. Takepron dosage: 15 MG (15 MG, 1 IN 1 D) PER ORAL. During the same period patient was treated with NEUROTROPIN. Patient was hospitalized. Patient recovered.
Takepron Side Effects Report #5060306-2
Takepron side effect was reported by a Consumer or non-health professional from JAPAN on July 10, 2006. Female patient, 60 years of age, was diagnosed with gastric ulcer and was treated with Takepron. After drug was administered, patient experienced the following side effects: abdominal distension, blood pressure increased, dyspnoea, face oedema, oedema peripheral, pruritus, rash
, renal failure acute. Takepron dosage: 30 MG (30 MG, 1 IN 1 D) PER ORAL. During the same period patient was treated with MUCOSTA. Patient recovered.Takepron Side Effects Report #5063666-1
Consumer or non-health professional from JAPAN reported Takepron side effect on May 31, 2006. Female patient was treated with Takepron. After drug was administered, patient experienced the following side effects: autoimmune disorder, encephalopathy. Takepron dosage: unknown. Patient was hospitalized. Patient recovered.
Takepron Side Effects Report #5072862-9
Takepron side effect was reported by a Health Professional from JAPAN on July 31, 2006. Female patient, 51 years of age, was treated with Takepron. After drug was administered, patient experienced the following side effects: cataract
, erythema multiforme, oesophageal ulcer, stevens-johnson syndrome. Takepron dosage: unknown. Patient recovered.Takepron Side Effects Report #5106841-X
Consumer or non-health professional from JAPAN reported Takepron side effect on Sept 06, 2006. Male patient, 70 years of age, was diagnosed with reflux oesophagitis and was treated with Takepron. After drug was administered, patient experienced the following side effects: oculomucocutaneous syndrome. Takepron dosage: 30 MG (30 MG, 1 IN 1 D) PER ORAL. During the same period patient was treated with LOXONIN. Patient was hospitalized. Patient recovered.
Takepron Side Effects Report #5147199-X
Takepron side effect was reported by a Consumer or non-health professional from JAPAN on Oct 31, 2006. Male patient, 78 years of age, was diagnosed with gastrointestinal haemorrhage and was treated with Takepron. After drug was administered, patient experienced the following side effects: condition aggravated, diabetic nephropathy, disease progression, renal impairment. Takepron dosage: 15 MG PER ORAL. During the same period patient was treated with FERROMIA, AMINOFLUID, LACTEC. Patient recovered.
Takepron Side Effects Report #5402854-9
Consumer or non-health professional from JAPAN reported Takepron side effect on July 23, 2007. Male patient, 56 years of age, was diagnosed with gastric ulcer and was treated with Takepron. After drug was administered, patient experienced the following side effects: blood creatine phosphokinase increased, oedema peripheral. Takepron dosage: 15 MG (15 MG, 1 IN 1 D); PER ORAL. During the same period patient was treated with LANSAP. Patient was hospitalized. Patient recovered.
Takepron Side Effects Report #5535124-9
Takepron side effect was reported by a Consumer or non-health professional from JAPAN on Nov 19, 2007. Female patient, 81 years of age, was diagnosed with reflux oesophagitis, fracture
, pain and was treated with Takepron. After drug was administered, patient experienced the following side effects: agranulocytosis, sepsis , upper respiratory tract inflammation. Takepron dosage: 15 MG (15 MG, 1 IN 1 D) PER ORAL. During the same period patient was treated with HISRACK, WARFARIN, SELEBEX, SENEVACUL, LENDORMIN. Patient died.Takepron Side Effects Report #5566480-3
Physician from JAPAN reported Takepron side effect on Dec 12, 2007. Female patient, 58 years of age, was diagnosed with gastric ulcer and was treated with Takepron. After drug was administered, patient experienced the following side effects: colitis ischaemic. Takepron dosage: unknown. During the same period patient was treated with FLAGYL, AMOXICILLIN TRIHYDRATE, MICARDIS. Patient was hospitalized. Patient recovered.
Takepron Side Effects Report #5577865-3
Takepron side effect was reported by a Physician from JAPAN on Dec 20, 2007. Female patient, weighting 82.45 lb, was diagnosed with acute myocardial infarction, postoperative analgesia, insomnia and was treated with Takepron. After drug was administered, patient experienced the following side effects: coma. Takepron dosage: 15 MG. During the same period patient was treated with PANALDINE, LIPITOR, ASPIRIN, MYSLEE, DIOVAN. Patient was hospitalized. Patient recovered.
Takepron Side Effects Report #5581654-3
Physician from JAPAN reported Takepron side effect on Dec 28, 2007. Female patient, 58 years of age, was diagnosed with gastric ulcer and was treated with Takepron. After drug was administered, patient experienced the following side effects: colitis ischaemic. Takepron dosage: unknown. During the same period patient was treated with FLAGYL, AMOXICILLIN TRIHYDRATE, MICARDIS. Patient was hospitalized. Patient recovered.
Takepron Side Effects Report #5603402-0
Takepron side effect was reported by a Consumer or non-health professional from JAPAN on Jan 16, 2008. Female patient, 76 years of age, was diagnosed with gastric ulcer, osteoporosis
and was treated with Takepron. After drug was administered, patient experienced the following side effects: agranulocytosis, altered state of consciousness, blood culture positive, disseminated intravascular coagulation, faecal incontinence, neutrophil count decreased, septic shock, staphylococcal infection , urinary incontinence . Takepron dosage: 30 MG (30 MG, 1 - 2) 35 MG (35 MG, 1 - 30 MG (30 MG, 1 IN 1 D), PER ORAL. During the same period patient was treated with FOSAMAC, PREDNISOLONE, MAGNESIUM OXIDE. Patient died.Takepron Side Effects Report #5620185-9
Health Professional from JAPAN reported Takepron side effect on Jan 29, 2008. Female patient, weighting 112.4 lb, was diagnosed with lacunar infarction, hyperlipidaemia and was treated with Takepron. After drug was administered, patient experienced the following side effects: embolic cerebral infarction. Takepron dosage: 15 MG. During the same period patient was treated with ASPIRIN, CLOPIDOGREL, ULCERLMIN, LIVALO. Patient was hospitalized. Patient recovered.
Takepron Side Effects Report #5676750-6
Takepron side effect was reported by a Health Professional from JAPAN on Mar 12, 2008. Female patient, 76 years of age, was diagnosed with gastric ulcer, osteoporosis
and was treated with Takepron. After drug was administered, patient experienced the following side effects: agranulocytosis, altered state of consciousness, antinuclear antibody positive, blood pressure decreased, disseminated intravascular coagulation, faecal incontinence, hepatic necrosis, hepatitis acute, malaise. Takepron dosage: 30 MG (30 MG,1 IN 1 D). During the same period patient was treated with FOSAMAX, PREDNISOLONE, MAGNESIUM OXIDE. Patient died.Takepron Side Effects Report #5701595-8
Pharmacist from JAPAN reported Takepron side effect on Apr 01, 2008. Male patient, weighting 160.9 lb, was diagnosed with prophylaxis against gastrointestinal ulcer, brain stem infarction and was treated with Takepron. After drug was administered, patient experienced the following side effects: c-reactive protein increased, pyrexia. Takepron dosage: unknown. During the same period patient was treated with PLAVIX. Patient recovered.
Takepron Side Effects Report #5724629-3
Takepron side effect was reported by a Consumer or non-health professional from JAPAN on Apr 23, 2008. Female patient, 74 years of age, was diagnosed with gastritis atrophic, hiatus hernia and was treated with Takepron. After drug was administered, patient experienced the following side effects: convulsion, myoglobinuria, rash erythematous, renal failure acute, rhabdomyolysis. Takepron dosage: 15 MG (15 MG, 1 IN 1 D), PER ORAL. During the same period patient was treated with TAKEPRON CAPSULES, PANSPORIN, THYRADIN, JOLETHIN, SELBEX, MECLOCELIN, INDERAL. Patient was hospitalized. Patient recovered.
Takepron Side Effects Report #5728425-2
Consumer or non-health professional from JAPAN reported Takepron side effect on Apr 24, 2008. Female patient, 76 years of age, was diagnosed with gastric ulcer, osteoporosis
and was treated with Takepron. After drug was administered, patient experienced the following side effects: agranulocytosis, disseminated intravascular coagulation, hepatic necrosis, hepatitis acute, malaise, neutrophil count decreased, septic shock, staphylococcal infection , white blood cell count decreased. Takepron dosage: 30 MG (30 MG, 1 IN 1 D) PER ORAL. During the same period patient was treated with FOSAMAC, PREDNISOLONE, MAGNESIUM OXIDE. Patient died.Takepron Side Effects Report #5789413-3
Takepron side effect was reported by a Consumer or non-health professional from JAPAN on June 16, 2008. Female patient, 86 years of age, was diagnosed with reflux oesophagitis and was treated with Takepron. After drug was administered, patient experienced the following side effects: abasia, asthenia, cardiac hypertrophy, colon cancer, dizziness
, insomnia, iron deficiency anaemia. Takepron dosage: 30 MG (30 MG, 1 IN 1 D). During the same period patient was treated with TAKEPRON CAPULES, TAKEPRON CAPULES, TAKEPRON CAPULES, TAKEPRON CAPULES, LANSOPRAZOLE, ZANTAC. Patient was hospitalized. Patient recovered.Takepron Side Effects Report #5814645-5
Consumer or non-health professional from JAPAN reported Takepron side effect on July 08, 2008. Female patient, 41 years of age, was diagnosed with gastrooesophageal reflux disease and was treated with Takepron. After drug was administered, patient experienced the following side effects: ectopic pregnancy. Takepron dosage: unknown. Patient was hospitalized. Patient recovered.
Takepron Side Effects Report #5884082-6
Takepron side effect was reported by a Physician from JAPAN on Sept 03, 2008. Female patient, 72 years of age, was diagnosed with prophylaxis against gastrointestinal ulcer and was treated with Takepron. After drug was administered, patient experienced the following side effects: bone marrow failure, decreased appetite, liver disorder. Takepron dosage: 30 MG (30 MG, 1 IN 1 D) PER ORAL. During the same period patient was treated with NEORAL, PREDNISOLONE, DOGMATYL. Patient was hospitalized. Patient recovered.
Takepron Side Effects Report #5912838-X
Consumer or non-health professional from JAPAN reported Takepron side effect on Sept 26, 2008. Male patient, 81 years of age, was diagnosed with duodenal ulcer, helicobacter infection, diabetes mellitus and was treated with Takepron. After drug was administered, patient experienced the following side effects: altered state of consciousness, blood glucose increased, diarrhoea, duodenal perforation, heart rate decreased, helicobacter infection, hyperhidrosis, hypoglycaemia, hypophagia. Takepron dosage: 30 MG (30 MG, 1 IN 1 D) PER ORAL. During the same period patient was treated with TAKEPRON OD, GLYBURIDE, CLARITHROMYCIN, SWACILLIN. Patient was hospitalized. Patient recovered.
Takepron Side Effects Report #5923793-0
Takepron side effect was reported by a Consumer or non-health professional from TAIWAN, PROVINCE OF CHINA on Oct 06, 2008. Female patient was diagnosed with gouty arthritis, ischaemic stroke, upper gastrointestinal haemorrhage and was treated with Takepron. After drug was administered, patient experienced the following side effects: multi-organ failure, septic shock, stevens-johnson syndrome, toxic epidermal necrolysis. Takepron dosage: unknown. During the same period patient was treated with TAKEPRON OD, TAKEPRON OD, CELECOXIB, CLOPIDOGREL. Patient died.
Takepron Side Effects Report #5978909-7
Consumer or non-health professional from JAPAN reported Takepron side effect on Nov 17, 2008. Female patient, 60 years of age, was treated with Takepron. After drug was administered, patient experienced the following side effects: agranulocytosis, pneumonia
. Takepron dosage: unknown. Patient died.Takepron Side Effects Report #6068803-8
Takepron side effect was reported by a Consumer or non-health professional from JAPAN on Jan 26, 2009. Male patient, 81 years of age, was diagnosed with helicobacter infection, diabetes mellitus and was treated with Takepron. After drug was administered, patient experienced the following side effects: altered state of consciousness, blood glucose increased, diarrhoea, duodenal ulcer perforation, gastrointestinal ulcer, glycosylated haemoglobin increased, heart rate decreased, hyperhidrosis. Takepron dosage: 30 MG (30 MG, 1 OM 1 D) PER ORAL, 60 MG MG (30 MG, 2 IN 1 D) PER ORAL. During the same period patient was treated with TAKEPRON OD, TAKEPRON OD, GLYBURIDE, CLARITIN. Patient was hospitalized. Patient recovered.
Takepron Side Effects Report #6075978-3
Physician from JAPAN reported Takepron side effect on Feb 04, 2009. Male patient, weighting 176.4 lb, was diagnosed with stent placement, acute myocardial infarction and was treated with Takepron. After drug was administered, patient experienced the following side effects: cholestasis, jaundice cholestatic. Takepron dosage: unknown. During the same period patient was treated with ASPIRIN, PLAVIX. Patient was hospitalized and became disabled. Patient recovered.
Takepron Side Effects Report #6080832-7
Takepron side effect was reported by a Physician from JAPAN on Feb 10, 2009. Male patient, 78 years of age, was diagnosed with prophylaxis, cerebral infarction and was treated with Takepron. After drug was administered, patient experienced the following side effects: hypereosinophilic syndrome, oedema peripheral, rash
. Takepron dosage: unknown. During the same period patient was treated with PLAVIX. Patient was hospitalized. Patient recovered.Takepron Side Effects Report #6094436-3
Physician from JAPAN reported Takepron side effect on Feb 19, 2009. Male patient, 78 years of age, was diagnosed with prophylaxis, cerebral infarction and was treated with Takepron. After drug was administered, patient experienced the following side effects: hypereosinophilic syndrome, oedema peripheral, rash
. Takepron dosage: unknown. During the same period patient was treated with PLAVIX. Patient was hospitalized. Patient recovered.Takepron Side Effects Report #4573917-5
Takepron side effect was reported by a Physician from on Jan 27, 2005. Male patient, 72 years of age, was diagnosed with gastric cancer, gastric ulcer haemorrhage and was treated with Takepron. After drug was administered, patient experienced the following side effects: abdominal pain upper, anuria, ascites, blood pressure increased, blood urine present, condition aggravated, gastric haemorrhage, haemodialysis. Takepron dosage: 30 MG (15 MG 2 IN 1 D). During the same period patient was treated with ACTOS, GLIMEPIRIDE, BROTIZOLAM. Patient recovered.
Takepron Side Effects Report #4749209-8
Consumer or non-health professional from JAPAN reported Takepron side effect on Aug 12, 2005. Female patient, 79 years of age, was diagnosed with gastritis erosive, helicobacter infection and was treated with Takepron. After drug was administered, patient experienced the following side effects: acidosis, blood pressure decreased, depressed level of consciousness, exchange blood transfusion, haemolytic anaemia, infection in an immunocompromised host, pneumonia
, pyrexia, respiratory disorder. Takepron dosage: 60 MG (60 MG, 1 D), PER ORAL. During the same period patient was treated with TAKEPRON OD, CLARITHROMYCIN, SAWASILLIN. Patient was hospitalized. Patient died.Takepron Side Effects Report #4758070-7
Takepron side effect was reported by a Consumer or non-health professional from JAPAN on Aug 25, 2005. Female patient, 79 years of age, was diagnosed with gastritis erosive, helicobacter infection and was treated with Takepron. After drug was administered, patient experienced the following side effects: acidosis, blood pressure decreased, condition aggravated, depressed level of consciousness, gastritis erosive, haemolytic anaemia, no therapeutic response, pneumonia
, respiratory disorder. Takepron dosage: unknown. During the same period patient was treated with TAKEPRON OD, TAKEPRON OD, TAKEPRON OD, CLARITHROMYCIN, SAWASILLIN. Patient was hospitalized. Patient died.Takepron Side Effects Report #4779088-4
Consumer or non-health professional from JAPAN reported Takepron side effect on Sept 21, 2005. Female patient, 65 years of age, was diagnosed with gastric ulcer and was treated with Takepron. After drug was administered, patient experienced the following side effects: abdominal pain upper, alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood lactate dehydrogenase increased, c-reactive protein increased, gamma-glutamyltransferase increased, hepatic function abnormal, myelodysplastic syndrome. Takepron dosage: 30 MG (30 MG, 1 IN 1 D); PER ORAL. During the same period patient was treated with DASEN, ULCHYONE, MIRIDACIN, SELBEX. Patient was hospitalized. Patient recovered.
Takepron Side Effects Report #4906931-8
Takepron side effect was reported by a Consumer or non-health professional from JAPAN on Feb 02, 2006. Male patient, 44 years of age, was diagnosed with stomach discomfort, nasopharyngitis and was treated with Takepron. After drug was administered, patient experienced the following side effects: ocular hyperaemia, rash
. Takepron dosage: 15 MG (15 MG, 1 IN 1 D), PER ORAL. During the same period patient was treated with RESPLEN, SELBEX. Patient was hospitalized. Patient recovered.Takepron Side Effects Report #4932309-7
Consumer or non-health professional from JAPAN reported Takepron side effect on Feb 24, 2006. Female patient, 60 years of age, was diagnosed with gastric ulcer and was treated with Takepron. After drug was administered, patient experienced the following side effects: eyelid oedema, hypersensitivity, oedema peripheral, pruritus, rash
, renal failure acute, weight increased. Takepron dosage: 30 MG (30 MG, 1 D) PER ORAL. During the same period patient was treated with MUCOSTA. Patient was hospitalized. Patient recovered.Takepron Side Effects Report #4972055-7
Takepron side effect was reported by a Consumer or non-health professional from JAPAN on Mar 27, 2006. Male patient, 65 years of age, was treated with Takepron. After drug was administered, patient experienced the following side effects: stevens-johnson syndrome. Takepron dosage: unknown. Patient died.
Takepron Side Effects Report #4976154-5
Consumer or non-health professional from JAPAN reported Takepron side effect on Mar 28, 2006. Male patient, 63 years of age, was diagnosed with gastric ulcer, gastric disorder, prophylaxis and was treated with Takepron. After drug was administered, patient experienced the following side effects: facial palsy, haematuria, haemodialysis, malaise, nephrosclerosis, renal failure acute, tubulointerstitial nephritis. Takepron dosage: 30 MG (30 MG, 1 IN 1 D). During the same period patient was treated with RABEPRAZOLE. Patient recovered.
Takepron Side Effects Report #4994201-1
Takepron side effect was reported by a Physician from JAPAN on Apr 27, 2006. Female patient, 75 years of age, was diagnosed with reflux oesophagitis and was treated with Takepron. After drug was administered, patient experienced the following side effects: oculomucocutaneous syndrome. Takepron dosage: 15 MG (15 MG, 1 IN 1 D). Patient recovered.
Takepron Side Effects Report #5015513-1
Consumer or non-health professional from JAPAN reported Takepron side effect on May 19, 2006. Male patient, 81 years of age, was diagnosed with gastric ulcer haemorrhage, prostate cancer
and was treated with Takepron. After drug was administered, patient experienced the following side effects: anaemia, cardiac failure, interstitial lung disease, pulmonary oedema, respiratory failure. Takepron dosage: 30 MG (30 MG, 1 IN 1 D), PER ORAL. During the same period patient was treated with LEUPLINFORECTION, CASODEX, MUCOSTA, SUCRALFATE, APLACE, SOLCOSERYL, AMINOFLUID, PESIN. Patient died.Takepron Side Effects Report #5016905-7
Takepron side effect was reported by a Consumer or non-health professional from JAPAN on May 17, 2006. Male patient, 39 years of age, was diagnosed with reflux oesophagitis and was treated with Takepron. After drug was administered, patient experienced the following side effects: fluid retention, pancreatic disorder. Takepron dosage: 15 MG (15 MG, 1 IN 1 D) PER ORAL. Patient was hospitalized. Patient recovered.
Takepron Side Effects Report #5020490-3
Consumer or non-health professional from JAPAN reported Takepron side effect on May 22, 2006. Male patient, 61 years of age, was diagnosed with reflux oesophagitis and was treated with Takepron. After drug was administered, patient experienced the following side effects: asthenia, blood creatine phosphokinase increased, muscular weakness. Takepron dosage: 15 MG (15 MG, 1 - 1 D) PER ORAL. During the same period patient was treated with OMEPRAZOLE, ASPIRIN, PLETAL, MUCOSTA. Patient was hospitalized. Patient recovered.
Takepron Side Effects Report #5023744-X
Takepron side effect was reported by a Physician from JAPAN on May 26, 2006. Male patient, 64 years of age, was diagnosed with reflux oesophagitis and was treated with Takepron. After drug was administered, patient experienced the following side effects: cardiac failure, pulmonary alveolar haemorrhage. Takepron dosage: 15 MG (15 MG, 1 IN 1 D). During the same period patient was treated with BUFFERIN, TICLOPIDINE, LOSARTAN POTASSIUM, SIGMART, MEXITIL, MAGNESIUM OXIDE. Patient recovered.