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Index of reports
> Cases resulting in life threatening events (4)
Below is the selection of adverse event reports related to Lotrel (Amlodipine / Benazepril) that includes cases resulting in life threatening events.
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 65 year old male receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-04-25
Patient: 65 year old male, weighing 109.5 kg (240.9 pounds)
Adverse reactions / side effects: LIP Swelling, Angioedema, Dyspnoea, Respiratory Disorder, Gout, Drug Hypersensitivity, Lens Implant, Pleurisy, Urticaria, Swollen Tongue
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Lotrel
Dosage: level 3
Administration route: Oral
Indication: Hypertension
Start date: 2005-06-28
End date: 2006-03-28
Lotrel
Dosage: level 1
Administration route: Oral
Start date: 2005-05-02
End date: 2005-06-02
Lotrel
Dosage: level 2
Administration route: Oral
Start date: 2005-06-03
End date: 2005-06-27
Cosopt
Ketorolac Tromethamine
Allopurinol
Dosage: 300 mg, unk
Administration route: Oral
Ofloxacin
Prednisolone
Other drugs received by patient: Aspirin; Avandia; Darvon-N; Hydrocodone; Acetaminophen; NPH Insulin; Insulin; Lasix; Metoprolol Succinate; Neurontin; Montelukast Sodium; Nitroglycerin; Simvastatin
Adverse event in 47 year old female receiving Lotrel (Amlodipine / Benazepril)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-02-21
Patient: 47 year old female, weighing 52.2 kg (114.8 pounds)
Adverse reactions / side effects: Phlebitis, Muscle Atrophy, Pain, Post Procedural Complication, Condition Aggravated, Appendicitis Perforated, Gangrene, Collapse of Lung, Haematotoxicity, Peritonitis, Complex Regional Pain Syndrome, Joint Sprain, Pleural Effusion
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
MS Contin
Dosage: 1 tablet twice daily-bid- po
Administration route: Oral
Indication: Complex Regional Pain Syndrome
Start date: 2000-08-20
End date: 2007-02-20
Lotrel
Dosage: 1 tab daily po
Administration route: Oral
Indication: Hypertension
Start date: 2001-01-01
End date: 2007-02-20
Adverse event in 72 year old female receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-01-26
Patient: 72 year old female, weighing 83.0 kg (182.6 pounds)
Adverse reactions / side effects: Dyspnoea, Dyspnoea Paroxysmal Nocturnal, Bundle Branch Block Left, Concomitant Disease Progression, Cardiomegaly, Oedema Peripheral, Orthopnoea, Cough, Cardiac Failure Congestive
Adverse event resulted in: life threatening event
Suspect drug(s):
Lotrel (Amlodipine / Benazepril)
Other drugs received by patient: Cozaar; Norvasc
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