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Index of reports
> Cases resulting in hospitalization (294)
> Cases with Blood Lactate Dehydrogenase Increased (27)
Below is the selection of adverse event reports related to Diovan (Valsartan) that includes cases resulting in hospitalization where reactions include blood lactate dehydrogenase increased.
Reports 1 - 25 of 27 Next >>
Adverse event in 35 year old male receiving Diovan (Valsartan)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-10-30
Patient: 35 year old male
Adverse reactions / side effects: Blood Alkaline Phosphatase Decreased, Vomiting, Blood Lactate Dehydrogenase Increased, Paralysis, Overdose, Fibrin Increased, Shock, White Blood Cell Count Increased
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Adalat
Dosage: oral
Administration route: Oral
Start date: 2007-08-18
End date: 2007-08-18
Allopurinol
Dosage: oral
Administration route: Oral
Indication: Self Mutilation
Start date: 2007-08-18
End date: 2007-08-18
Carvedilol
Dosage: oral
Administration route: Oral
Start date: 2007-08-18
End date: 2007-08-18
Diovan
Dosage: oral
Administration route: Oral
Start date: 2007-08-18
End date: 2007-08-18
Olmesartan Medoxomil
Dosage: oral
Administration route: Oral
Start date: 2007-08-18
End date: 2007-08-18
Adverse event in 87 year old female receiving Diovan (Valsartan)
Reported by a physician from Japan on 2007-10-30
Patient: 87 year old female
Adverse reactions / side effects: Blood Alkaline Phosphatase Increased, Monoplegia, Blood Lactate Dehydrogenase Increased, Lymphopenia, Dysarthria, Blood Creatinine Decreased, Gamma-Glutamyltransferase Increased, Cerebral Infarction, RED Blood Cell Count Decreased, C-Reactive Protein Increased, Oedema Peripheral, Nuclear Magnetic Resonance Imaging Abnormal, Asthenia, White Blood Cell Count Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Diovan (Valsartan)
Other drugs received by patient: Aspirin; Amlodipine; Aricept; Predonine; Amaryl
Adverse event in 63 year old male receiving Diovan (Valsartan)
Reported by a physician from Japan on 2007-10-25
Patient: 63 year old male, weighing 72.0 kg (158.4 pounds)
Adverse reactions / side effects: Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Hepatic Function Abnormal, Hepatitis Acute, Urticaria, Blood Lactate Dehydrogenase Increased, Alanine Aminotransferase Increased, Jaundice Cholestatic, Leukocytoclastic Vasculitis, Pruritus Generalised, Aspartate Aminotransferase Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Diovan (Valsartan)
Other drugs received by patient: Aspirin; Famotidine; Tamsulosin Hydrochloride; Apolakete; Bladderon; Melbin; Magnesium Oxide; Prednisolone; Tamsulosin HCL
Adverse event in 89 year old female receiving Diovan (Valsartan)
Reported by a physician from Japan on 2007-10-22
Patient: 89 year old female, weighing 42.0 kg (92.4 pounds)
Adverse reactions / side effects: Eyelid Oedema, Atelectasis, Blood Bilirubin Increased, Respiratory Disorder, Hepatic Function Abnormal, Hyperkalaemia, Atrioventricular Block Complete, Sinus Bradycardia, Haematocrit Decreased, Gamma-Glutamyltransferase Increased, RED Blood Cell Count Decreased, Pleural Effusion, Blood Sodium Increased, Sinus Arrest, Blood Creatinine Increased, Blood Glucose Increased, Decreased Appetite, White Blood Cell Count Decreased, Blood Alkaline Phosphatase Increased, Blood Urea Increased, Hypotension, Blood Lactate Dehydrogenase Increased, Alanine Aminotransferase Increased, General Physical Health Deterioration, Blood Potassium Increased, Haemoglobin Decreased, Sick Sinus Syndrome, Cardiac Failure, Cardiac Pacemaker Insertion, Electrocardiogram Abnormal, Aspartate Aminotransferase Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Aricept
Dosage: 5mg
Administration route: Oral
Start date: 2007-03-16
Diltiazem HCL
Dosage: 100 mg/day
Administration route: Oral
Indication: Angina Pectoris
Start date: 2007-06-15
End date: 2007-08-17
Diovan
Dosage: 40 mg/day
Administration route: Oral
Indication: Hypertension
Start date: 2007-07-20
End date: 2007-08-17
Other drugs received by patient: Famogast; Urso 250; Trepibutone; Coniel; Nitroderm; Sigmart; Lasix; Doxazosin Mesylate
Adverse event in 35 year old male receiving Diovan (Valsartan)
Reported by a individual with unspecified qualification from United Kingdom on 2007-10-19
Patient: 35 year old male
Adverse reactions / side effects: Blood Alkaline Phosphatase Decreased, Vomiting, Hypotension, Blood Lactate Dehydrogenase Increased, Paralysis, Gastrointestinal Tube Insertion, Respiratory Rate Decreased, Overdose, Heart Rate Decreased, White Blood Cell Count Increased, Shock, Fibrin Increased
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Adalat
Dosage: 40 mg x 40 tablets
Administration route: Oral
Start date: 2007-08-18
End date: 2007-08-18
Allopurinol
Dosage: 100 mg x 32 tablets
Administration route: Oral
Start date: 2007-08-18
End date: 2007-08-18
Carvedilol
Dosage: 10 mg x 32 tablets
Administration route: Oral
Indication: Self Mutilation
Start date: 2007-08-18
End date: 2007-08-18
Diovan
Dosage: 40mgx 8 tablets
Administration route: Oral
Start date: 2007-08-18
End date: 2007-08-18
Olmetec
Dosage: 20 mg x 74 tablets
Administration route: Oral
Start date: 2007-08-18
End date: 2007-08-18
Other drugs received by patient: Alcohol
Adverse event in 63 year old male receiving Diovan (Valsartan)
Reported by a physician from Japan on 2007-10-18
Patient: 63 year old male, weighing 72.0 kg (158.4 pounds)
Adverse reactions / side effects: Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Hepatic Function Abnormal, Hepatitis Acute, Urticaria, Blood Lactate Dehydrogenase Increased, Alanine Aminotransferase Increased, Jaundice Cholestatic, Leukocytoclastic Vasculitis, Pruritus Generalised, Aspartate Aminotransferase Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Diovan (Valsartan)
Other drugs received by patient: Aspirin; Famotidine; Tamsulosin Hydrochloride; Apolakete; Bladderon; Melbin; Magnesium Oxide; Prednisolone; Tamsulosin HCL
Adverse event in 87 year old female receiving Diovan (Valsartan)
Reported by a physician from Japan on 2007-10-09
Patient: 87 year old female
Adverse reactions / side effects: Blood Alkaline Phosphatase Increased, Monoplegia, Blood Lactate Dehydrogenase Increased, Lymphopenia, Dysarthria, Blood Creatinine Decreased, Gamma-Glutamyltransferase Increased, Cerebral Infarction, RED Blood Cell Count Decreased, C-Reactive Protein Increased, Oedema Peripheral, Nuclear Magnetic Resonance Imaging Abnormal, Asthenia, White Blood Cell Count Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Diovan (Valsartan)
Other drugs received by patient: Aspirin; Amlodipine; Aricept; Predonine; Amaryl
Adverse event in 35 year old male receiving Diovan (Valsartan)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-10-09
Patient: 35 year old male
Adverse reactions / side effects: Blood Alkaline Phosphatase Decreased, Vomiting, Blood Lactate Dehydrogenase Increased, Paralysis, Overdose, Fibrin Increased, Shock, White Blood Cell Count Increased
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Adalat
Dosage: 1920mg per day
Administration route: Oral
Indication: Self Mutilation
Start date: 2007-08-18
End date: 2007-08-18
Allopurinol
Dosage: 32000mg per day
Administration route: Oral
Indication: Self Mutilation
Start date: 2007-08-18
End date: 2007-08-18
Artist
Dosage: 320mg per day
Administration route: Oral
Indication: Self Mutilation
Start date: 2007-08-18
End date: 2007-08-18
Diovan
Dosage: 320mg per day
Administration route: Oral
Indication: Self Mutilation
Start date: 2007-08-18
End date: 2007-08-18
Olmetec
Dosage: 1480mg per day
Administration route: Oral
Indication: Self Mutilation
Start date: 2007-08-18
End date: 2007-08-18
Adverse event in 35 year old male receiving Diovan (Valsartan)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-10-09
Patient: 35 year old male
Adverse reactions / side effects: Blood Alkaline Phosphatase Decreased, Vomiting, Blood Lactate Dehydrogenase Increased, Paralysis, Overdose, Fibrin Increased, Shock, White Blood Cell Count Increased
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Adalat
Dosage: 1920mg per day
Administration route: Oral
Indication: Self Mutilation
Start date: 2007-08-18
End date: 2007-08-18
Allopurinol
Dosage: 32000mg per day
Administration route: Oral
Indication: Self Mutilation
Start date: 2007-08-18
End date: 2007-08-18
Artist
Dosage: 320mg per day
Administration route: Oral
Indication: Self Mutilation
Start date: 2007-08-18
End date: 2007-08-18
Diovan
Dosage: 320mg per day
Administration route: Oral
Indication: Self Mutilation
Start date: 2007-08-18
End date: 2007-08-18
Olmetec
Dosage: 1480mg per day
Administration route: Oral
Indication: Self Mutilation
Start date: 2007-08-18
End date: 2007-08-18
Adverse event in 73 year old female receiving Diovan (Valsartan)
Reported by a physician from Japan on 2007-10-08
Patient: 73 year old female, weighing 57.0 kg (125.4 pounds)
Adverse reactions / side effects: Upper Respiratory Tract Inflammation, Fall, Weight Increased, RED Blood Cell Count Decreased, C-Reactive Protein Increased, Hepatic Atrophy, Gamma-Glutamyltransferase Increased, Blood Uric Acid Increased, Oedema, RIB Fracture, Blood Glucose Increased, Cough, Hepatic Cirrhosis, Blood Pressure Increased, Renal Disorder, Blood Lactate Dehydrogenase Increased, Ascites, Haemoglobin Decreased, Aspartate Aminotransferase Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Diovan
Dosage: 80 mg, bid
Administration route: Oral
Indication: Hypertension
Start date: 2007-02-15
End date: 2007-05-25
Diovan
Dosage: 40 mg
Administration route: Oral
Start date: 2004-06-11
End date: 2004-08-05
Diovan
Dosage: 80 mg/day
Administration route: Oral
Start date: 2004-08-06
Other drugs received by patient: Thyradin; Thyradin; Neurovitan; Frandol; Lipidil; Novorapid; Atelec; Pursennid; Coniel
Adverse event in 78 year old male receiving Diovan (Valsartan)
Reported by a physician from Japan on 2007-07-26
Patient: 78 year old male, weighing 52.0 kg (114.4 pounds)
Adverse reactions / side effects: Jaundice, Eosinophil Count Decreased, Blood Bilirubin Increased, Nasopharyngitis, Alanine Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Liver Disorder, Weight Increased, Haemoglobin Decreased, Haematocrit Decreased, Malaise, Gamma-Glutamyltransferase Increased, RED Blood Cell Count Decreased, Aspartate Aminotransferase Increased, Peritoneal Effusion
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Diovan
Dosage: 40 mg/day
Administration route: Oral
Indication: Hypertension
Start date: 2006-11-01
Flomox
Dosage: 300 mg/day
Administration route: Oral
Indication: Upper Respiratory Tract Inflammation
Start date: 2007-05-21
End date: 2007-05-25
Kakkon-TO
Dosage: 7.5 g/day
Administration route: Oral
Indication: Upper Respiratory Tract Inflammation
Start date: 2007-05-21
End date: 2007-05-25
Adverse event in 84 year old female receiving Diovan (Valsartan)
Reported by a physician from Japan on 2007-07-25
Patient: 84 year old female, weighing 38.0 kg (83.6 pounds)
Adverse reactions / side effects: Blood Bilirubin Increased, Blood Alkaline Phosphatase Increased, Hepatic Function Abnormal, Alanine Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Purpura, Eosinophilia, Cholelithiasis, Gamma-Glutamyltransferase Increased, Aspartate Aminotransferase Increased, Platelet Count Decreased, Thrombocytopenia, Bilirubin Conjugated Increased
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Diovan (Valsartan)
Other drugs received by patient: Spiriva; Frandol
Adverse event in 78 year old male receiving Diovan (Valsartan)
Reported by a physician from Japan on 2007-07-24
Patient: 78 year old male, weighing 52.0 kg (114.4 pounds)
Adverse reactions / side effects: Jaundice, Eosinophil Count Decreased, Blood Bilirubin Increased, Nasopharyngitis, Alanine Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Liver Disorder, Weight Increased, Haemoglobin Decreased, Haematocrit Decreased, Malaise, Gamma-Glutamyltransferase Increased, RED Blood Cell Count Decreased, Aspartate Aminotransferase Increased, Peritoneal Effusion
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Diovan
Dosage: 40 mg/day
Administration route: Oral
Indication: Hypertension
Start date: 2006-11-01
Flomox
Dosage: 300 mg/day
Administration route: Oral
Indication: Upper Respiratory Tract Inflammation
Start date: 2007-05-21
End date: 2007-05-25
Kakkon-TO
Dosage: 7.5 g/day
Administration route: Oral
Indication: Upper Respiratory Tract Inflammation
Start date: 2007-05-21
End date: 2007-05-25
Adverse event in 87 year old female receiving Diovan (Valsartan)
Reported by a physician from Japan on 2007-07-23
Patient: 87 year old female, weighing 35.0 kg (77.0 pounds)
Adverse reactions / side effects: Blood Bilirubin Increased, Coagulopathy, Cholestasis, Coma, Hepatic Failure, Gastrointestinal Tube Insertion, Liver Disorder, Hepatic Encephalopathy, Subdural Haematoma, Malaise, Gamma-Glutamyltransferase Increased, Cholecystitis, Gallbladder Disorder, Prothrombin Time Ratio Increased, Alanine Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Tremor, Cholelithiasis, Anorexia, Aspartate Aminotransferase Increased, Gallbladder Polyp
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Amaryl
Dosage: 1 mg/day
Administration route: Oral
Indication: Diabetes Mellitus
Start date: 2007-04-01
End date: 2007-05-17
Aspirin
Dosage: 100 mg/day
Administration route: Oral
Indication: Angina Pectoris
Start date: 2007-04-01
End date: 2007-05-26
Diovan
Dosage: 40 mg/day
Administration route: Oral
Indication: Hypertension
Start date: 2006-06-14
End date: 2007-05-23
Norvasc
Dosage: 2.5 mg/day
Administration route: Oral
Indication: Hypertension
Start date: 1999-05-01
End date: 2007-05-25
Other drugs received by patient: Roxatidine Acetate HCL; Nateglinide; Triazolam; Lisinopril; Lisinopril
Adverse event in 79 year old male receiving Diovan (Valsartan)
Reported by a physician from Japan on 2007-07-09
Patient: 79 year old male
Adverse reactions / side effects: Blood Bilirubin Increased, Pyrexia, Liver Disorder, Malaise, Haematocrit Decreased, RED Blood Cell Count Decreased, Gamma-Glutamyltransferase Increased, White Blood Cell Count Increased, Blood Glucose Increased, Lymphocyte Count Decreased, Blood Alkaline Phosphatase Increased, Blood Urea Increased, Pneumonia, Blood Lactate Dehydrogenase Increased, Alanine Aminotransferase Increased, Urine Output Decreased, Haemoglobin Decreased, Aspartate Aminotransferase Increased, Platelet Count Decreased
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Diovan (Valsartan)
Other drugs received by patient: Lendormin; Pariet; Norvasc; Rinderon; Aspirin; Clarithromycin; Rizaben
Adverse event in 51 year old male receiving Diovan (Valsartan)
Reported by a physician from Japan on 2007-06-27
Patient: 51 year old male
Adverse reactions / side effects: Drug Eruption, Alanine Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Toxic Epidermal Necrolysis, Cerebral Haemorrhage, Hypoalbuminaemia, Stevens-Johnson Syndrome, Infection
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Diovan
Dosage: 1 dosage forms, 1 in 1 d, oral
Administration route: Oral
Indication: Hypertension
Start date: 2006-12-31
End date: 2007-03-17
Zonisamide
Dosage: 200 mg, 2 in 1 d, oral
Administration route: Oral
Indication: Cerebral Haemorrhage
Start date: 2007-01-04
End date: 2007-02-07
Other drugs received by patient: Takepron (Lansoprazole) (Lansoprazole); NI (Magnesium Oxide) (Magnesium Oxide); Pursennid (Sennoside) (Senna Leaf)
Adverse event in 51 year old male receiving Diovan (Valsartan)
Reported by a physician from Japan on 2007-06-19
Patient: 51 year old male
Adverse reactions / side effects: Alanine Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Toxic Epidermal Necrolysis, Varicella, Mycoplasma Infection, Staphylococcal Infection, NO Therapeutic Response, Hypoalbuminaemia, Dermatitis Exfoliative, White Blood Cell Count Increased, Infection
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Diovan
Dosage: 1 dosage forms, 1 in 1 d, oral
Administration route: Oral
Indication: Hypertension
Start date: 2006-12-31
End date: 2007-03-17
Zonisamide
Dosage: 200 mg, 2 in 1 d, oral
Administration route: Oral
Indication: Cerebral Haemorrhage
Start date: 2007-01-04
End date: 2007-02-07
Other drugs received by patient: Lansoprazole; NI (Magnesium Oxide); Pursennid (Sennoside) (Senna Leaf)
Adverse event in 51 year old male receiving Diovan (Valsartan)
Reported by a physician from Japan on 2007-05-29
Patient: 51 year old male
Adverse reactions / side effects: Drug Eruption, Alanine Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, NO Therapeutic Response, Toxic Epidermal Necrolysis
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Diovan
Dosage: 1 in 1 d; oral
Administration route: Oral
Indication: Hypertension
Start date: 2006-12-31
End date: 2007-03-17
Diovan
Dosage: 1 in 1 d; oral
Administration route: Oral
Indication: Hypertension
Start date: 2006-12-31
End date: 2007-03-17
Zonisamide
Dosage: 200 mg, 2 in 1 d; oral
Administration route: Oral
Indication: Cerebral Haemorrhage
Start date: 2007-01-04
End date: 2007-02-07
Zonisamide
Dosage: 200 mg, 2 in 1 d; oral
Administration route: Oral
Indication: Cerebral Haemorrhage
Start date: 2007-01-04
End date: 2007-02-07
Other drugs received by patient: Takepron (Lansoprazole) (Lansoprazole); NI (Magnesium Oxide ) (Magnesium Oxide); Pursennid (Sennoside) (Senna Leaf); Takepron (Lansoprazole) (Lansoprazole); NI (Magnesium Oxide ) (Magnesium Oxide); Pursennid (Sennoside) (Senna Leaf)
Adverse event in 51 year old male receiving Diovan (Valsartan)
Reported by a physician from Japan on 2007-05-22
Patient: 51 year old male
Adverse reactions / side effects: Drug Eruption, Alanine Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Toxic Epidermal Necrolysis, Pyrexia, Dermatitis Exfoliative, Stevens-Johnson Syndrome
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Diovan
Dosage: 1 in 1 d, oral
Administration route: Oral
Indication: Hypertension
Start date: 2006-12-31
End date: 2007-03-17
Zonisamide
Dosage: 200 mg, 2 in 1 d, oral
Administration route: Oral
Indication: Cerebral Haemorrhage
Start date: 2007-01-04
End date: 2007-02-07
Other drugs received by patient: Takepron (Lansoprazole) (Lansoprazole); NI (Magnesium Oxide) (Magnesium Oxide); Pursennid (Sennoside) (Senna Leaf)
Adverse event in 51 year old male receiving Diovan (Valsartan)
Reported by a physician from Japan on 2007-05-14
Patient: 51 year old male
Adverse reactions / side effects: Drug Eruption, Alanine Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Toxic Epidermal Necrolysis, Pyrexia, White Blood Cell Count Increased
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Diovan
Dosage: 1 in 1 d, oral
Administration route: Oral
Indication: Hypertension
Start date: 2006-12-31
End date: 2007-03-17
Zonisamide
Dosage: 200 mg, 2 in 1 d, oral
Administration route: Oral
Indication: Cerebral Haemorrhage
Start date: 2007-01-04
End date: 2007-02-07
Other drugs received by patient: Lansoprazole; (Magnesium Oxide) (Magnesium Oxide); Pursennid (Sennoside) (Senna Leaf)
Adverse event in 74 year old male receiving Diovan (Valsartan)
Reported by a physician from Japan on 2007-03-19
Patient: 74 year old male
Adverse reactions / side effects: Blood Bilirubin Increased, Hepatic Function Abnormal, C-Reactive Protein Increased, Gamma-Glutamyltransferase Increased, Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Prothrombin Time Shortened, Bilirubin Conjugated Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Cardenalin
Dosage: 2 mg, bid
Administration route: Oral
Indication: Hypertension
Diovan
Dosage: 80 mg/day
Administration route: Oral
Indication: Hypertension
Start date: 2006-04-01
End date: 2007-01-09
Adverse event in 74 year old male receiving Diovan (Valsartan)
Reported by a physician from Japan on 2007-03-06
Patient: 74 year old male
Adverse reactions / side effects: Blood Bilirubin Increased, Hepatic Function Abnormal, C-Reactive Protein Increased, Gamma-Glutamyltransferase Increased, Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Prothrombin Time Shortened, Bilirubin Conjugated Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Cardenalin
Dosage: 2 mg, bid
Administration route: Oral
Indication: Hypertension
Diovan
Dosage: 80 mg/day
Administration route: Oral
Indication: Hypertension
Start date: 2006-04-01
End date: 2007-01-01
Adverse event in 76 year old male receiving Diovan (Valsartan)
Reported by a pharmacist from Japan on 2007-03-05
Patient: 76 year old male
Adverse reactions / side effects: Choking Sensation, PO2 Decreased, Interstitial Lung Disease, C-Reactive Protein Increased, Palpitations, Tracheostomy, Blood Bicarbonate Increased, Cell Marker Increased, Acute Respiratory Failure, White Blood Cell Count Increased, Oxygen Saturation Decreased, Blood Alkaline Phosphatase Increased, Dyspnoea, Blood Lactate Dehydrogenase Increased, Lung Disorder, Hypertension, Inflammation
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Diovan (Valsartan)
Other drugs received by patient: Adalat; Actos; Lasix
Adverse event in 76 year old male receiving Diovan (Valsartan)
Reported by a pharmacist from Japan on 2007-02-27
Patient: 76 year old male
Adverse reactions / side effects: Choking Sensation, PO2 Decreased, Interstitial Lung Disease, C-Reactive Protein Increased, Palpitations, Tracheostomy, Blood Bicarbonate Increased, Cell Marker Increased, Acute Respiratory Failure, White Blood Cell Count Increased, Oxygen Saturation Decreased, Blood Alkaline Phosphatase Increased, Dyspnoea, Blood Lactate Dehydrogenase Increased, Lung Disorder, Hypertension, Inflammation
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Diovan (Valsartan)
Other drugs received by patient: Adalat; Actos; Lasix
Adverse event in 76 year old male receiving Diovan (Valsartan)
Reported by a pharmacist from Japan on 2007-02-19
Patient: 76 year old male
Adverse reactions / side effects: Choking Sensation, PO2 Decreased, Interstitial Lung Disease, C-Reactive Protein Increased, Palpitations, Tracheostomy, Blood Bicarbonate Increased, Acute Respiratory Failure, Cell Marker Increased, Oxygen Saturation Decreased, White Blood Cell Count Increased, Blood Alkaline Phosphatase Increased, Dyspnoea, Blood Lactate Dehydrogenase Increased, Lung Disorder, Hypertension, Inflammation
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Actos
Dosage: 15 mg/day
Administration route: Oral
Indication: Diabetes Mellitus
Start date: 2005-08-29
End date: 2006-10-16
Adalat
Dosage: 40 mg/ day
Administration route: Oral
Indication: Hypertension
Start date: 2005-08-29
End date: 2006-10-16
Diovan
Dosage: 80 mg, tid
Administration route: Oral
Indication: Hypertension
Start date: 2005-08-25
End date: 2006-10-16
Lasix
Dosage: 20 mg/day
Administration route: Oral
Indication: Hypertension
Start date: 2005-08-29
End date: 2006-10-16
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