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Index of reports
> Cases resulting in hospitalization (57)
Below is the selection of adverse event reports related to Lotrel (Amlodipine / Benazepril) that includes cases resulting in hospitalization.
Reports 1 - 25 of 57 Next >>
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 female receiving Lotrel (Amlodipine / Benazepril)
Reported by a individual with unspecified qualification from United States on 2007-10-19
Patient: female
Adverse reactions / side effects: Angioedema, Dyspnoea, Urticaria, Pharyngolaryngeal Pain, Hearing Impaired, Sleep Apnoea Syndrome, Pharyngitis
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotrel (Amlodipine / Benazepril)
Adverse event in 64 year old female receiving Lotrel (Amlodipine / Benazepril)
Reported by a individual with unspecified qualification from United States on 2007-10-17
Patient: 64 year old female
Adverse reactions / side effects: Abdominal Pain, Dizziness, White Blood Cell Count Increased, Blood Glucose Increased, Lymphocyte Count Decreased, Neutrophil Count Increased, Angioedema, Vomiting, Nausea, Hypotension, Intestinal Congestion, Haematochezia, Dysstasia, Blood Potassium Decreased, Diarrhoea, Blood Urea Decreased, Colitis
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotrel (Amlodipine / Benazepril)
Other drugs received by patient: Norvasc
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 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 2007-10-05
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 64 year old female receiving Lotrel (Amlodipine / Benazepril)
Reported by a individual with unspecified qualification from United States on 2007-10-04
Patient: 64 year old female
Adverse reactions / side effects: Abdominal Pain, Haemorrhage, Diarrhoea Haemorrhagic, Dizziness, White Blood Cell Count Increased, Lymphocyte Count Decreased, Blood Glucose Increased, Vomiting, Neutrophil Count Increased, Angioedema, Nausea, Hypotension, Intestinal Congestion, Haematochezia, Dysstasia, Blood Potassium Decreased, Diarrhoea, Small Bowel Angioedema, Colitis, Blood Urea Decreased, Gastrointestinal Oedema
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotrel (Amlodipine / Benazepril)
Other drugs received by patient: Norvasc
Adverse event in 77 year old female receiving Lotrel (Amlodipine / Benazepril)
Reported by a individual with unspecified qualification from United States on 2007-10-02
Patient: 77 year old female
Adverse reactions / side effects: Renal Failure, Laboratory Test Abnormal, Dyspnoea, Renal Artery Stent Placement, Gait Disturbance, Feeling Abnormal, Asthenia
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Lotrel (Amlodipine / Benazepril)
Adverse event in 53 year old female receiving Lotrel (Amlodipine / Benazepril)
Reported by a individual with unspecified qualification from United States on 2007-07-23
Patient: 53 year old female
Adverse reactions / side effects: Chest Pain, Coronary Artery Occlusion, Heart Rate Increased, Dizziness, Nuclear Magnetic Resonance Imaging Brain Abnormal, Headache
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotrel
Dosage: 5/20mg, qd
Administration route: Oral
Indication: Hypertension
Zelnorm
Dosage: 6 mg, qd
Administration route: Oral
Indication: Irritable Bowel Syndrome
Start date: 2004-11-01
End date: 2007-05-11
Other drugs received by patient: Duragesic-100; Nexium; Valium; Lorazepam; Lexapro; Zetia; Methylprednisolone; Darvocet
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 female receiving Lotrel (Amlodipine / Benazepril)
Reported by a individual with unspecified qualification from United States on 2007-07-13
Patient: female
Adverse reactions / side effects: Arrhythmia
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotrel (Amlodipine / Benazepril)
Adverse event in female receiving Lotrel (Amlodipine / Benazepril)
Reported by a individual with unspecified qualification from United States on 2007-07-13
Patient: female
Adverse reactions / side effects: Arrhythmia
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotrel (Amlodipine / Benazepril)
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 82 year old male receiving Lotrel (Amlodipine / Benazepril)
Reported by a consumer/non-health professional from United States on 2007-07-06
Patient: 82 year old male
Adverse reactions / side effects: Nausea, Aphasia, Dizziness, Muscular Weakness, Hypoaesthesia, Cerebrovascular Accident
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotrel (Amlodipine / Benazepril)
Other drugs received by patient: Glucovance
Adverse event in 75 year old female receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-07-02
Patient: 75 year old female, weighing 77.7 kg (170.9 pounds)
Adverse reactions / side effects: Back Pain, Spinal Compression Fracture, Hypotension, Hyponatraemia, Inappropriate Antidiuretic Hormone Secretion, Convulsion
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotrel
Dosage: level 1
Administration route: Oral
Indication: Hypertension
Start date: 2004-08-01
End date: 2004-09-05
Lotrel
Dosage: level 2
Administration route: Oral
Start date: 2004-09-06
End date: 2004-10-04
Lotrel
Dosage: unk, level 3
Administration route: Oral
Start date: 2004-10-05
End date: 2004-11-15
Lotrel
Dosage: unk, level 3
Administration route: Oral
Start date: 2004-12-05
Other drugs received by patient: Toprol-XL; Amiodarone; Protonix; Lexapro; Aspirin; Klor-CON; Bentyl
Adverse event in 68 year old female receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-07-02
Patient: 68 year old female, weighing 77.7 kg (170.9 pounds)
Adverse reactions / side effects: Fluid Overload, Dyspnoea, Diabetic Nephropathy, Concomitant Disease Progression, Dyspnoea Exertional, Renal Failure, Proteinuria, Orthopnoea, Oedema, Cardiac Failure Congestive
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotrel
Dosage: unk, level 3
Administration route: Oral
Indication: Hypertension
Start date: 2006-02-27
End date: 2007-05-17
Lotrel
Dosage: level 1
Administration route: Oral
Start date: 2004-01-09
End date: 2004-02-11
Lotrel
Dosage: level 2
Administration route: Oral
Start date: 2004-02-12
End date: 2004-03-17
Lotrel
Dosage: unk, level 3
Administration route: Oral
Start date: 2004-03-18
End date: 2004-12-27
Lotrel
Dosage: unk, no treatment
Start date: 2004-12-28
End date: 2005-01-01
Lotrel
Dosage: unk, level 3
Administration route: Oral
Start date: 2005-01-02
End date: 2006-02-22
Lotrel
Dosage: unk, no treatment
Start date: 2006-02-23
End date: 2006-02-26
Other drugs received by patient: Labetalol HCL; Lasix
Adverse event in 68 year old female receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-06-29
Patient: 68 year old female, weighing 77.7 kg (170.9 pounds)
Adverse reactions / side effects: Fluid Overload, Dyspnoea, Diabetic Nephropathy, Concomitant Disease Progression, Dyspnoea Exertional, Renal Failure, Proteinuria, Orthopnoea, Oedema, Cardiac Failure Congestive
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotrel
Dosage: unk, level 3
Administration route: Oral
Indication: Hypertension
Start date: 2006-02-27
End date: 2007-05-17
Lotrel
Dosage: level 1
Administration route: Oral
Start date: 2004-01-09
End date: 2004-02-11
Lotrel
Dosage: level 2
Administration route: Oral
Start date: 2004-02-12
End date: 2004-03-17
Lotrel
Dosage: unk, level 3
Administration route: Oral
Start date: 2004-03-18
End date: 2004-12-27
Lotrel
Dosage: unk, no treatment
Start date: 2004-12-28
End date: 2005-01-01
Lotrel
Dosage: unk, level 3
Administration route: Oral
Start date: 2005-01-02
End date: 2006-02-22
Lotrel
Dosage: unk, no treatment
Start date: 2006-02-23
End date: 2006-02-26
Other drugs received by patient: Labetalol HCL; Lasix
Adverse event in 72 year old female receiving Lotrel (Amlodipine / Benazepril)
Reported by a pharmacist from United States on 2007-06-27
Patient: 72 year old female, weighing 31.8 kg (70.0 pounds)
Adverse reactions / side effects: Myalgia, Blood Creatine Phosphokinase Increased, Asthenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Simvastatin
Dosage: at bedtime po
Administration route: Oral
Indication: Diabetes Mellitus
Start date: 2007-04-10
End date: 2007-05-06
Simvastatin
Dosage: at bedtime po
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2007-04-10
End date: 2007-05-06
Lotrel
Dosage: 5mg/20mg qday po prior to march 2007
Administration route: Oral
Indication: Hypertension
Start date: 2007-03-01
Adverse event in 69 year old male receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-06-18
Patient: 69 year old male, weighing 93.9 kg (206.6 pounds)
Adverse reactions / side effects: Back Pain, Surgery, Nausea, Dizziness, Hyperhidrosis, Concomitant Disease Progression, Arthritis
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotrel
Dosage: level 1
Administration route: Oral
Indication: Hypertension
Start date: 2004-03-11
Lotrel
Dosage: level 2
Administration route: Oral
Lotrel
Dosage: unknown
Administration route: Oral
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 84 year old male receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-05-30
Patient: 84 year old male, weighing 75.0 kg (165.0 pounds)
Adverse reactions / side effects: Abdominal Pain, Dysphagia, Pneumonia Aspiration, Head Injury, Muscular Weakness, Pyrexia, Fall, Lumbar Spinal Stenosis, Paraesthesia, Anaemia of Chronic Disease, Oliguria, Intervertebral Disc Degeneration, Anuria, Renal Failure Acute
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
Adverse event in 79 year old male receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-05-30
Patient: 79 year old male, weighing 81.1 kg (178.4 pounds)
Adverse reactions / side effects: Syncope, Vomiting, Nausea, Dizziness
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotrel
Dosage: level 1
Administration route: Oral
Indication: Hypertension
Start date: 2004-06-16
End date: 2004-07-13
Lotrel
Dosage: level 2
Administration route: Oral
Start date: 2004-07-14
Other drugs received by patient: Crestor; Metoprolol Succinate; Aspirin
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