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Index of reports
> Cases resulting in a serious event (116)
> Cases with Blood Creatinine Increased (19)
Below is the selection of adverse event reports related to Lotrel (Amlodipine / Benazepril) that includes cases resulting in a serious event where reactions include blood creatinine increased.
Adverse event in 70 year old female receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-10-26
Patient: 70 year old female, weighing 72.9 kg (160.4 pounds)
Adverse reactions / side effects: Facial Palsy, Hyperkalaemia, Headache, Hemiparesis, Fall, Dizziness, Blood Creatinine Increased, Blood Urea Increased, Anaemia, Muscular Weakness, Cerebrovascular Accident, Concomitant Disease Progression, Carotid Artery Stenosis, Renal Failure, Vertigo, Hypertension
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotrel
Dosage: level 1
Administration route: Oral
Indication: Hypertension
Start date: 2004-08-02
Lotrel
Dosage: level 3
Administration route: Oral
Lotrel
Dosage: no treatment
Lotrel
Dosage: level 3
Administration route: Oral
Hydrochlorothiazide
Administration route: Oral
End date: 2007-04-11
Other drugs received by patient: Lipitor; Atenolol; Aspirin; Glipizide; Trazodone HCL; Zoloft; Lantus
Adverse event in 70 year old female receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-10-25
Patient: 70 year old female, weighing 72.9 kg (160.4 pounds)
Adverse reactions / side effects: Facial Palsy, Hyperkalaemia, Headache, Hemiparesis, Fall, Dizziness, Blood Creatinine Increased, Blood Urea Increased, Anaemia, Muscular Weakness, Cerebrovascular Accident, Concomitant Disease Progression, Carotid Artery Stenosis, Renal Failure, Vertigo, Hypertension
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotrel
Dosage: level 1
Administration route: Oral
Indication: Hypertension
Start date: 2004-08-02
Lotrel
Dosage: level 3
Administration route: Oral
Lotrel
Dosage: no treatment
Lotrel
Dosage: level 3
Administration route: Oral
Hydrochlorothiazide
Administration route: Oral
End date: 2007-04-11
Other drugs received by patient: Lipitor; Atenolol; Aspirin; Glipizide; Trazodone HCL; Zoloft; Lantus
Adverse event in 70 year old female receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-10-15
Patient: 70 year old female, weighing 72.9 kg (160.4 pounds)
Adverse reactions / side effects: Blood Urea Increased, Hyperkalaemia, Anaemia, Concomitant Disease Progression, Fall, Renal Failure, Vertigo, Dizziness, Blood Creatinine Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotrel
Dosage: level 1
Administration route: Oral
Indication: Hypertension
Start date: 2004-08-02
Lotrel
Dosage: level 3
Administration route: Oral
Lotrel
Dosage: no treatment
Lotrel
Dosage: level 3
Administration route: Oral
Hydrochlorothiazide
Administration route: Oral
End date: 2007-04-11
Other drugs received by patient: Lipitor; Atenolol; Aspirin; Glipizide; Trazodone HCL; Zoloft; Lantus
Adverse event in 76 year old male receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-10-15
Patient: 76 year old male, weighing 84.8 kg (186.6 pounds)
Adverse reactions / side effects: Stent Placement, Angioplasty, Fall, Incontinence, Skin Ulcer, Urinary Retention, Blood Creatinine Increased, Diabetes Mellitus Inadequate Control, Hypovolaemia, Stent Occlusion, Pain in Extremity, Clavicle Fracture, Urinary Tract Infection, Hypotension, Hyperglycaemia, Coronary Angioplasty, Concomitant Disease Progression, Stress, Arterial Bypass Operation, Osteoarthritis, Renal Failure, Blood Potassium Decreased, Impaired Healing, Dehydration, Peripheral Arterial Occlusive Disease, Angiopathy, Leukocytosis, Normochromic Normocytic Anaemia
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotrel
Dosage: level 1
Administration route: Oral
Indication: Hypertension
Start date: 2004-05-18
Lotrel
Dosage: level 3
Administration route: Oral
Start date: 2006-12-27
End date: 2007-07-01
Other drugs received by patient: Metformin; Simvastatin; Plavix; Aspirin; Insulin; Glucophage; Zocor; Flomax
Adverse event in 76 year old male receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-10-05
Patient: 76 year old male, weighing 84.8 kg (186.6 pounds)
Adverse reactions / side effects: Stent Placement, Angioplasty, Fall, Incontinence, Skin Ulcer, Urinary Retention, Blood Creatinine Increased, Hypovolaemia, Diabetes Mellitus Inadequate Control, Stent Occlusion, Pain in Extremity, Clavicle Fracture, Urinary Tract Infection, Hyperglycaemia, Hypotension, Concomitant Disease Progression, Stress, Arterial Bypass Operation, Osteoarthritis, Renal Failure, Impaired Healing, Blood Potassium Decreased, Dehydration, Peripheral Arterial Occlusive Disease, Normochromic Normocytic Anaemia, Leukocytosis, Angiopathy
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotrel
Dosage: level 1
Administration route: Oral
Indication: Hypertension
Start date: 2004-05-18
Lotrel
Dosage: level 3
Administration route: Oral
Start date: 2006-12-27
End date: 2007-07-01
Other drugs received by patient: Metformin HCL; Simvastatin; Plavix; Aspirin; Insulin; Glucophage; Zocor; Flomax
Adverse event in 70 year old male receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-10-05
Patient: 70 year old male
Adverse reactions / side effects: Weight Decreased, Bile Duct Stent Insertion, Vomiting, Nausea, Abdominal Pain Upper, Cholelithiasis, Blood Amylase Increased, Pancreatitis, Cholecystectomy, Lipase Increased, Biliary Sphincterotomy, Blood Creatinine Increased, Renal Failure Acute
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotrel
Dosage: level 1
Administration route: Oral
Indication: Hypertension
Start date: 2004-04-13
End date: 2004-05-12
Lotrel
Dosage: level 3
Administration route: Oral
Start date: 2007-05-13
End date: 2007-04-10
Lotrel
Dosage: unk, level 3
Administration route: Oral
Start date: 2006-04-11
End date: 2007-08-22
Other drugs received by patient: Vitamin CAP; Tramadol HCL; Aspirin; Meloxicam; Terazosin HCL; Simvastatin; Amlodipine; Omeprazole; Omega 3 Fish OIL; Glucosamine
Adverse event in 84 year old male receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-07-20
Patient: 84 year old male, weighing 75.0 kg (165.0 pounds)
Adverse reactions / side effects: Abdominal Pain, Pneumonia Aspiration, Head Injury, Pyrexia, Fall, Hypokalaemia, Lumbar Spinal Stenosis, Hypomagnesaemia, Chest Pain, Hypoxia, Intervertebral Disc Degeneration, Blood Creatinine Increased, Anuria, Renal Failure Acute, Dysphagia, Hyperglycaemia, Muscular Weakness, Paraesthesia, Oliguria, Gait Disturbance, Leukocytosis
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotrel
Dosage: level 1
Administration route: Oral
Indication: Hypertension
Start date: 2005-02-22
Lotrel
Dosage: level 3
Administration route: Oral
Other drugs received by patient: Flomax; Detrol; Lipitor; Calcium Carbonate W / Vitamin D NOS; Allopurinol; Diflucan; Lisinopril; Norvasc; Celexa; Phoslo; Aranesp; Nephro-Vite; Folic Acid; Lasix; Lantus; Insulin; Metoprolol Tartrate; Protonix; Hytrin
Adverse event in 70 year old female receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-07-11
Patient: 70 year old female, weighing 72.9 kg (160.4 pounds)
Adverse reactions / side effects: Blood Urea Increased, Hyperkalaemia, Anaemia, Concomitant Disease Progression, Fall, Renal Failure, Vertigo, Dizziness, Blood Creatinine Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotrel
Dosage: level 1
Administration route: Oral
Indication: Hypertension
Start date: 2004-08-02
Lotrel
Dosage: level 3
Administration route: Oral
Hydrochlorothiazide
Administration route: Oral
End date: 2007-04-11
Other drugs received by patient: Lipitor; Atenolol; Aspirin; Glipizide; Trazodone HCL; Zoloft; Lantus
Adverse event in 70 year old female receiving Lotrel (Amlodipine / Benazepril)
Reported by a individual with unspecified qualification from United States on 2007-07-11
Patient: 70 year old female
Adverse reactions / side effects: Confusional State, Body Temperature Increased, Restlessness, Hypotension, Blood Potassium Increased, Hyponatraemia, Delirium, Herpes Zoster, Renal Failure, Hypoalbuminaemia, Blood Creatinine Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotrel
Dosage: unk, qd
Administration route: Oral
Indication: Hypertension
End date: 2006-04-01
Lotrel
Dosage: unk, qd
Administration route: Oral
End date: 2006-04-01
Other drugs received by patient: Fosamax; Advair Diskus 100 / 50; Xopenex; Spiriva ^pfizer^; Singulair; Prednisone; Oxygen
Adverse event in 84 year old male receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-06-11
Patient: 84 year old male, weighing 75.0 kg (165.0 pounds)
Adverse reactions / side effects: Abdominal Pain, Pneumonia Aspiration, Head Injury, Pyrexia, Fall, Hypokalaemia, Lumbar Spinal Stenosis, Hypomagnesaemia, Chest Pain, Hypoxia, Intervertebral Disc Degeneration, Blood Creatinine Increased, Anuria, Renal Failure Acute, Dysphagia, Hyperglycaemia, Muscular Weakness, Paraesthesia, Oliguria, Gait Disturbance, Leukocytosis
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotrel
Dosage: level 1
Administration route: Oral
Indication: Hypertension
Start date: 2005-02-22
Lotrel
Dosage: level 3
Administration route: Oral
Other drugs received by patient: Flomax; Detrol; Lipitor; Calcium Carbonate W / Vitamin D NOS; Allopurinol; Diflucan; Lisinopril; Norvasc; Celexa; Phoslo; Aranesp; Nephro-Vite; Folic Acid; Lasix; Lantus; Insulin; Metoprolol Succinate; Protonix; Hytrin
Adverse event in 77 year old female receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-05-06
Patient: 77 year old female, weighing 75.0 kg (165.0 pounds)
Adverse reactions / side effects: Abdominal Pain, Blood Urea Increased, Gastrointestinal Haemorrhage, Nausea, Hypotension, Atrial Fibrillation, Hyponatraemia, Hyperhidrosis, Haematochezia, Diverticulum, Haematocrit Decreased, Dizziness, Colitis, Asthenia, Blood Creatinine Increased, White Blood Cell Count Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotrel
Dosage: level 1
Administration route: Oral
Indication: Hypertension
Start date: 2004-04-23
Lotrel
Dosage: level 3
Administration route: Oral
End date: 2007-04-05
Coumadin
Indication: Atrial Fibrillation
Other drugs received by patient: Atenolol
Adverse event in 77 year old female receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-05-04
Patient: 77 year old female, weighing 75.0 kg (165.0 pounds)
Adverse reactions / side effects: Abdominal Pain, Blood Urea Increased, Gastrointestinal Haemorrhage, Nausea, Hypotension, Atrial Fibrillation, Hyponatraemia, Hyperhidrosis, Haematochezia, Diverticulum, Haematocrit Decreased, Dizziness, Colitis, Asthenia, Blood Creatinine Increased, White Blood Cell Count Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotrel
Dosage: level 1
Administration route: Oral
Indication: Hypertension
Start date: 2004-04-23
Lotrel
Dosage: level 3
Administration route: Oral
End date: 2007-04-05
Coumadin
Indication: Atrial Fibrillation
Other drugs received by patient: Atenolol
Adverse event in 58 year old female receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-05-02
Patient: 58 year old female
Adverse reactions / side effects: Blood Creatinine Increased
Suspect drug(s):
Lotrel (Amlodipine / Benazepril)
Adverse event in 77 year old female receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-04-30
Patient: 77 year old female, weighing 75.0 kg (165.0 pounds)
Adverse reactions / side effects: Abdominal Pain, Colitis Ischaemic, Blood Urea Increased, Gastrointestinal Haemorrhage, Nausea, Atrial Fibrillation, Hyponatraemia, Hyperhidrosis, Haematochezia, Diverticulum, Haematocrit Decreased, Dizziness, Blood Creatinine Increased, Asthenia, White Blood Cell Count Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotrel
Dosage: level 1
Administration route: Oral
Indication: Hypertension
Start date: 2004-04-23
Lotrel
Dosage: level 3
Administration route: Oral
End date: 2007-04-05
Other drugs received by patient: Atenolol; Coumadin
Adverse event in 65 year old male receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-04-24
Patient: 65 year old male, weighing 90.0 kg (198.0 pounds)
Adverse reactions / side effects: Renal Failure, Urine Albumin / Creatinine Ratio Increased, Blood Creatinine Increased, Concomitant Disease Progression, Sleep Apnoea Syndrome
Suspect drug(s):
Lotrel
Dosage: unk, level 1
Administration route: Oral
Indication: Hypertension
Start date: 2005-03-10
Lotrel
Dosage: off study drug
Start date: 2006-04-18
End date: 2006-05-23
Lotrel
Dosage: level 3
Administration route: Oral
Start date: 2006-05-24
End date: 2007-03-12
Hydrochlorothiazide
Dosage: unknown
Start date: 2006-01-05
End date: 2006-03-06
Other drugs received by patient: Minipress; Glucotrol XL; Metformin Hydrochloride; Atenolol
Adverse event in 63 year old female receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-04-13
Patient: 63 year old female, weighing 63.1 kg (138.8 pounds)
Adverse reactions / side effects: Confusional State, Electrocardiogram ST-T Change, Chills, Drug Interaction, Mental Status Changes, Hyperhidrosis, Dizziness, Pharyngolaryngeal Pain, Microangiopathy, Blood Creatinine Increased, White Blood Cell Count Increased, Hypovolaemia, Acute Prerenal Failure, Hypotension, Encephalopathy, Hypertension
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotrel
Dosage: level 1
Administration route: Oral
Indication: Hypertension
Start date: 2004-04-16
End date: 2004-04-29
Lotrel
Dosage: level 2
Administration route: Oral
Start date: 2004-04-30
End date: 2005-11-17
Imdur
Dosage: 30 mg, qd
Administration route: Oral
Indication: Coronary Artery Disease
Start date: 2002-01-15
End date: 2005-11-17
Nitroglycerin
Neuroton
Dosage: 600 mg, tid
Administration route: Oral
Indication: Restless Legs Syndrome
End date: 2005-11-17
Other drugs received by patient: Lipitor; Amitriptyline HCL; Oxytrol; Oyster Shell Calcium; Aspirin; Vitamin CAP; Nexium; Rhinocort; Serevent; Singulair; Magnesium Oxide; Glyburide; Pulmicort; Zyrtec; Metformin; Albuterol; Plavix
Adverse event in 65 year old male receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-03-23
Patient: 65 year old male, weighing 90.0 kg (198.0 pounds)
Adverse reactions / side effects: Urine Albumin / Creatinine Ratio Increased, Blood Creatinine Increased, Sleep Apnoea Syndrome
Suspect drug(s):
Lotrel
Dosage: unk, level 1
Administration route: Oral
Indication: Hypertension
Start date: 2005-03-10
Lotrel
Dosage: off study drug
Start date: 2006-04-18
End date: 2006-05-23
Lotrel
Dosage: level 3
Administration route: Oral
Start date: 2006-05-24
End date: 2007-03-12
Hydrochlorothiazide
Dosage: unknown
Start date: 2006-01-05
End date: 2006-03-06
Other drugs received by patient: Minipress; Glucotrol XL; Metformin Hydrochloride; Atenolol
Adverse event in 73 year old male receiving Lotrel (Amlodipine / Benazepril)
Reported by a consumer/non-health professional from United States on 2007-03-10
Patient: 73 year old male
Adverse reactions / side effects: Protein Urine Present, Blood Creatinine Increased, Cough
Suspect drug(s):
Lotrel (Amlodipine / Benazepril)
Adverse event in 63 year old male receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-01-26
Patient: 63 year old male, weighing 88.4 kg (194.6 pounds)
Adverse reactions / side effects: Renal Failure, Fatigue, Dyspnoea, Hypotension, Dizziness, Blood Creatinine Increased, Acute Prerenal Failure
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotrel (Amlodipine / Benazepril)
Other drugs received by patient: Maxzide; Norvasc; Insulin
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