|
This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Lotrel (Amlodipine / Benazepril). Click on the relevant link below to view a selection of reports according to the event's seriousness level and/or the nature of the side effect / adverse reaction. Or scroll down to view a sample of recent reports further on this page.
Our database includes reports from Jan 2007 to Dec 2007. The information is not vetted and should not be cosidered as verified clinical evidence.
All cases (126)
Cases resulting in a serious event (116)
Cases resulting in life threatening events (4)
Cases resulting in hospitalization (57)
Cases resulting in other serious reactions (67)
Below is a sample of reports where side effects / adverse reactions may be related to Lotrel (Amlodipine / Benazepril). For a complete list and/or a specific selection of reports, please use the links in the index above.
Adverse event in male receiving Lotrel (Amlodipine / Benazepril)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-30
Patient: male, weighing 68.4 kg (150.5 pounds)
Adverse reactions / side effects: Blood Pressure Increased, Abnormal Dreams, Back Pain, Drug Hypersensitivity, Chest Pain
Suspect drug(s):
Lotrel (Amlodipine / Benazepril)
Adverse event in 85 year old female receiving Lotrel (Amlodipine / Benazepril)
Reported by a consumer/non-health professional from United States on 2007-10-29
Patient: 85 year old female
Adverse reactions / side effects: Heart Rate Irregular, Cough
Suspect drug(s):
Lotrel (Amlodipine / Benazepril)
Adverse event in male receiving Lotrel (Amlodipine / Benazepril)
Reported by a consumer/non-health professional from United States on 2007-10-26
Patient: male
Adverse reactions / side effects: Neuritis
Suspect drug(s):
Lotrel
Indication: Hypertension
Hydrochlorothiazide
Dosage: 25 mg, unk
Indication: Hypertension
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 consumer/non-health professional from United States on 2007-10-25
Patient: female
Adverse reactions / side effects: Loss of Consciousness
Suspect drug(s):
Lotrel (Amlodipine / Benazepril)
Adverse event in receiving Lotrel (Amlodipine / Benazepril)
Reported by a pharmacist from United States on 2007-10-25
Patient:
Adverse reactions / side effects: Pharmaceutical Product Complaint
Suspect drug(s):
Lotrel
Dosage: 5mg/20mg qd po
Administration route: Oral
Indication: Hypertension
Amlodipine / Benazepril 5MG / 20mg Novartis / Sandoz
Dosage: 5mg/20mg qd po
Administration route: Oral
Indication: Hypertension
Adverse event in 80 year old male receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-10-23
Patient: 80 year old male, weighing 79.4 kg (174.6 pounds)
Adverse reactions / side effects: Sensation of Heaviness, Oedema Peripheral
Suspect drug(s):
Lotrel (Amlodipine / Benazepril)
Adverse event in 59 year old female receiving Lotrel (Amlodipine / Benazepril)
Reported by a individual with unspecified qualification from United States on 2007-10-23
Patient: 59 year old female
Adverse reactions / side effects: White Blood Cell Count Decreased, Palpitations, Chest Pain, Proteinuria, Microalbuminuria, Asthenia, Pain in JAW
Suspect drug(s):
Lotensin
Dosage: 40 mg, qd
Administration route: Oral
Indication: Hypertension
Start date: 2007-02-23
Lotrel
Dosage: unk, qd
Administration route: Oral
Indication: Hypertension
Start date: 2007-09-01
End date: 2007-09-01
Other drugs received by patient: Aspirin; Humalog; Vytorin; Lantus
Adverse event in 52 year old male receiving Lotrel (Amlodipine / Benazepril)
Reported by a consumer/non-health professional from United States on 2007-10-22
Patient: 52 year old male, weighing 99.8 kg (219.5 pounds)
Adverse reactions / side effects: Rash Generalised, Retching, Pharmaceutical Product Complaint, Rash Pruritic
Suspect drug(s):
Metoprolol Tartrate
Dosage: 5/10 1 a day po
Administration route: Oral
Indication: Drug Therapy
Start date: 2007-07-01
End date: 2007-10-17
Amlodipine Besylate and Benazepril HCL
Dosage: 50 mg 1 a day po
Administration route: Oral
Indication: Hypertension
Start date: 2007-07-01
End date: 2007-10-17
Toprol-XL
Lotrel
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 93 year old female receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-10-18
Patient: 93 year old female
Adverse reactions / side effects: Malaise, Colon Cancer, Palpitations, Oedema Peripheral, Joint Stiffness
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 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 female receiving Lotrel (Amlodipine / Benazepril)
Reported by a consumer/non-health professional from United States on 2007-10-12
Patient: female
Adverse reactions / side effects: Blood Potassium Abnormal, Blood Pressure Fluctuation, Asthenia
Suspect drug(s):
Lotrel (Amlodipine / Benazepril)
Adverse event in female receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-10-10
Patient: female, weighing 1.0 kg (2.2 pounds)
Adverse reactions / side effects: Small FOR Dates Baby, Congenital Hand Malformation, Premature Baby
Suspect drug(s):
Viramune
Indication: HIV Infection
Start date: 2006-10-01
Epzicom
Indication: HIV Infection
Start date: 2006-10-01
Lotrel
End date: 2007-06-19
Procardia XL
Start date: 2007-06-19
Adverse event in 79 year old male receiving Lotrel (Amlodipine / Benazepril)
Reported by a pharmacist from United States on 2007-10-10
Patient: 79 year old male, weighing 82.6 kg (181.6 pounds)
Adverse reactions / side effects: Blood Bilirubin Increased, Abdominal Pain, Vomiting, Hypotension, Food Poisoning, Chills, Transaminases Increased, Hepatic Enzyme Increased
Suspect drug(s):
Lotrel (Amlodipine / Benazepril)
Adverse event in female receiving Lotrel (Amlodipine / Benazepril)
Reported by a consumer/non-health professional from United States on 2007-10-10
Patient: female, weighing 0.7 kg (1.5 pounds)
Adverse reactions / side effects: Congenital Hand Malformation, Drug Exposure During Pregnancy, Premature Baby, Amniotic Cavity Disorder
Suspect drug(s):
Epzicom
Indication: Drug USE FOR Unknown Indication
Start date: 2006-10-01
Lotrel
Indication: Drug USE FOR Unknown Indication
End date: 2007-06-19
Other drugs received by patient: Viramune; Procardia XL
Adverse event in 57 year old female receiving Lotrel (Amlodipine / Benazepril)
Reported by a individual with unspecified qualification from United States on 2007-10-09
Patient: 57 year old female, weighing 102.1 kg (224.5 pounds)
Adverse reactions / side effects: Diplopia, Visual Disturbance, Feeling Abnormal
Suspect drug(s):
Lotrel
Dosage: once day po x 3d
Administration route: Oral
Indication: Hypertension
Start date: 2007-06-22
End date: 2007-06-25
Lotrel
Dosage: one daily po x 14d
Administration route: Oral
Indication: Hypertension
Start date: 2007-06-26
Adverse event in 63 year old female receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-10-05
Patient: 63 year old female, weighing 68.5 kg (150.7 pounds)
Adverse reactions / side effects: Blood Pressure Systolic Decreased, Glomerular Filtration Rate Decreased, Decreased Activity, Hypotension, Asthenia
Suspect drug(s):
Tekturna
Dosage: 150 mg, qd, oral; 75 mg, qd, oral; 150 mg, qd, oral
Administration route: Oral
Indication: Hypertension
Start date: 2007-05-08
End date: 2007-05-01
Tekturna
Dosage: 150 mg, qd, oral; 75 mg, qd, oral; 150 mg, qd, oral
Administration route: Oral
Indication: Hypertension
Start date: 2007-05-01
Lotrel
Dosage: 10/20 mg, qhs, oral
Administration route: Oral
Indication: Hypertension
Start date: 2006-08-23
Diovan
Dosage: in the am, qd, oral
Administration route: Oral
Other drugs received by patient: Diovan HCT; Clonidine
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)
|
