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Index of reports
> Cases resulting in a serious event (116)
> Cases with Dizziness (25)
Below is the selection of adverse event reports related to Lotrel (Amlodipine / Benazepril) that includes cases resulting in a serious event where reactions include dizziness.
Reports 1 - 25 of 25 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 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 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 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 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 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 female receiving Lotrel (Amlodipine / Benazepril)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-06-22
Patient: female, weighing 109.3 kg (240.5 pounds)
Adverse reactions / side effects: Dizziness, Paraesthesia
Suspect drug(s):
Lotrel (Amlodipine / Benazepril)
Adverse event in 51 year old female receiving Lotrel (Amlodipine / Benazepril)
Reported by a individual with unspecified qualification from United States on 2007-06-21
Patient: 51 year old female
Adverse reactions / side effects: Vomiting, Nausea, Hypotension, Dizziness, Headache, Eating Disorder, Loss of Consciousness
Suspect drug(s):
Lotrel
Dosage: 10/20 mg, qd
Administration route: Oral
Indication: Hypertension
Start date: 2007-05-17
End date: 2007-05-22
Lotrel
Dosage: 5/20 mg, qd
Administration route: Oral
Start date: 2007-05-23
End date: 2007-06-09
Other drugs received by patient: Benicar
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 48 year old female receiving Lotrel (Amlodipine / Benazepril)
Reported by a consumer/non-health professional from United States on 2007-06-05
Patient: 48 year old female
Adverse reactions / side effects: Hot Flush, Panic Attack, Electrocardiogram Abnormal, Dizziness
Suspect drug(s):
Lotrel
Dosage: unk, qd
Administration route: Oral
Indication: Hypertension
Start date: 2006-12-01
End date: 2007-05-25
Diovan
Dosage: unk, qd
Administration route: Oral
Indication: Hypertension
Start date: 2006-12-01
End date: 2007-05-25
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
Adverse event in 53 year old female receiving Lotrel (Amlodipine / Benazepril)
Reported by a individual with unspecified qualification from United States on 2007-05-29
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 16mg TAB; Darvocet-N 100
Adverse event in 79 year old male receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-05-29
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
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 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 female receiving Lotrel (Amlodipine / Benazepril)
Reported by a consumer/non-health professional from United States on 2007-04-17
Patient: female, weighing 56.2 kg (123.6 pounds)
Adverse reactions / side effects: Blood Pressure Increased, Dizziness, Eye Pain
Suspect drug(s):
Depo-Medrol
Indication: Pain
Start date: 2007-03-07
End date: 2007-03-07
Depo-Medrol
Indication: Swelling
Depo-Medrol
Indication: Osteoarthritis
Valsartan
Indication: Hypertension
Start date: 2007-03-09
End date: 2007-04-04
Lotrel
Dosage: text:5/10 mg; 5/10 mg-freq:qd:every day
Indication: Hypertension
Other drugs received by patient: Vitamins; Xanax
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 pharmacist from United States on 2007-04-05
Patient: 65 year old male, weighing 71.9 kg (158.2 pounds)
Adverse reactions / side effects: Hypotension, Presyncope, Dizziness, Bradycardia
Adverse event resulted in: hospitalization
Suspect drug(s):
Doxazosin Mesylate
Dosage: 2 mg qd po
Administration route: Oral
Indication: Benign Prostatic Hyperplasia
Lotrel
Dosage: 10 mg/ 20 mg qd po
Administration route: Oral
Indication: Hypertension
Adverse event in 93 year old female receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-03-07
Patient: 93 year old female, weighing 74.8 kg (164.6 pounds)
Adverse reactions / side effects: Nausea, Dizziness, Headache, Depression, Gait Disturbance, Tremor
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotrel (Amlodipine / Benazepril)
Other drugs received by patient: Lipitor; Atenolol; Synthroid; Zantac
Adverse event in 93 year old female receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-03-07
Patient: 93 year old female, weighing 74.8 kg (164.6 pounds)
Adverse reactions / side effects: Nausea, Dizziness, Headache, Depression, Gait Disturbance, Tremor
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotrel (Amlodipine / Benazepril)
Other drugs received by patient: Lipitor; Atenolol; Synthroid; Zantac
Adverse event in 75 year old male receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-02-01
Patient: 75 year old male, weighing 83.6 kg (183.9 pounds)
Adverse reactions / side effects: Productive Cough, Atelectasis, Pulmonary Hypertension, Electrocardiogram T Wave Amplitude Decreased, Stent Placement, Chronic Obstructive Pulmonary Disease, Disease Progression, Fatigue, Dyspnoea Exertional, Oedema Peripheral, Hypoxia, Dizziness, Oedema, Cardiac Failure Congestive, Electrocardiogram T Wave Inversion, Coronary Artery Disease, Diastolic Dysfunction, Bronchitis, Asthenia, Arterial Stenosis
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotrel
Dosage: unk, level 3
Administration route: Oral
Indication: Hypertension
Start date: 2004-11-15
End date: 2007-01-19
Lotrel
Dosage: level 3
Administration route: Oral
Start date: 2004-09-08
End date: 2004-10-11
Lotrel
Dosage: level 2
Administration route: Oral
Start date: 2004-10-12
End date: 2004-11-14
Other drugs received by patient: Amaryl; Metformin HCL; Atenolol; Fexofenadine; Aspirin; Tricor; Clonidine; Ranitidine; Sulindac; Lipitor; Valium; Lasix
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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