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Index of reports
> Cases resulting in other serious reactions (9)
Below is the selection of adverse event reports related to Lotensin (Benazepril) that includes cases resulting in other serious reactions.
Adverse event in 59 year old female receiving Lotensin (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 38 year old male receiving Lotensin (Benazepril)
Reported by a consumer/non-health professional from China on 2007-10-16
Patient: 38 year old male
Adverse reactions / side effects: Heart Rate Decreased
Suspect drug(s):
Lotensin (Benazepril)
Other drugs received by patient: Aspirin; JIN KUI Shen QI Pill
Adverse event in male receiving Lotensin (Benazepril)
Reported by a consumer/non-health professional from United States on 2007-10-12
Patient: male, weighing 104.8 kg (230.6 pounds)
Adverse reactions / side effects: Renal Function Test Abnormal, Vision Blurred, Blood Glucose Increased
Suspect drug(s):
Chantix
Indication: EX-Smoker
Glibenclamide Tablet
Indication: Diabetes Mellitus Inadequate Control
Lotensin
Indication: Hypertension
Lotensin
Other drugs received by patient: Norvasc; Darvocet; Simvastatin; Acetylsalicylic Acid
Adverse event in 65 year old male receiving Lotensin (Benazepril)
Reported by a physician from United States on 2007-10-08
Patient: 65 year old male, weighing 98.9 kg (217.5 pounds)
Adverse reactions / side effects: Pharyngeal Oedema, Tongue Oedema, Stent Placement, Coronary Artery Disease, Percutaneous Coronary Intervention, Myocardial Infarction
Suspect drug(s):
Benazepril Hydrochloride
Dosage: 40 mg, bid
Administration route: Oral
Indication: Hypertension
End date: 2007-09-12
Lotensin
Dosage: 40 mg, bid
Administration route: Oral
Indication: Hypertension
Start date: 1987-01-01
Other drugs received by patient: Glucovance; Byetta; Actos; Levemir; Valium; Plavix; Lipitor; Hydrochlorothiazide; Potassium Chloride; Bisoprolol Fumarate
Adverse event in 49 year old male receiving Lotensin (Benazepril)
Reported by a consumer/non-health professional from China on 2007-07-16
Patient: 49 year old male
Adverse reactions / side effects: Blood Bilirubin Increased, Gamma-Glutamyltransferase Increased, Aspartate Aminotransferase Increased, Alanine Aminotransferase Increased, Urine Protein / Creatinine Ratio Increased, Urine Bilirubin Increased
Suspect drug(s):
Lotensin (Benazepril)
Other drugs received by patient: Adalat
Adverse event in 28 year old female receiving Lotensin (Benazepril)
Reported by a consumer/non-health professional from China on 2007-03-08
Patient: 28 year old female
Adverse reactions / side effects: Normal Newborn, Caesarean Section, Drug Exposure During Pregnancy
Suspect drug(s):
Lotensin (Benazepril)
Adverse event in 57 year old female receiving Lotensin (Benazepril)
Reported by a individual with unspecified qualification from United States on 2007-02-20
Patient: 57 year old female
Adverse reactions / side effects: LIP Swelling
Suspect drug(s):
Lotensin (Benazepril)
Adverse event in 64 year old male receiving Lotensin (Benazepril)
Reported by a physician from United States on 2007-02-13
Patient: 64 year old male
Adverse reactions / side effects: Urinary Tract Obstruction, Blood Creatine Phosphokinase Increased, Renal Failure, Rhabdomyolysis, Urinary Tract Infection, Hepatic Failure
Adverse event resulted in: hospitalization
Suspect drug(s):
Casodex
Administration route: Oral
Coumadin
Crestor
Administration route: Oral
Floxmax
Lotensin
Norvasc
Adverse event in 61 year old female receiving Lotensin (Benazepril)
Reported by a physician from United States on 2007-02-06
Patient: 61 year old female, weighing 111.0 kg (244.2 pounds)
Adverse reactions / side effects: Back Pain, Drooling, Aphasia, Cerebrovascular Accident, Fall, Dysarthria, Limb Injury, Hypoaesthesia Facial, Hypertension
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotensin
Dosage: 5 mg, qd
Indication: Hypertension
Start date: 1986-01-01
Lotensin
Dosage: 10 mg, qd
Lotensin
Dosage: 20 mg, bid
Start date: 2004-01-01
Other drugs received by patient: Synthroid
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