|
Index of reports
> Cases resulting in other serious reactions (67)
> Cases with Abdominal Pain (7)
Below is the selection of adverse event reports related to Lotrel (Amlodipine / Benazepril) that includes cases resulting in other serious reactions where reactions include abdominal pain.
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 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 84 year old male receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-05-29
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 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 73 year old male receiving Lotrel (Amlodipine / Benazepril)
Reported by a physician from United States on 2007-05-02
Patient: 73 year old male
Adverse reactions / side effects: Jaundice, Abdominal Pain, Blood Bilirubin Increased, Vomiting, Chest Discomfort, Intubation, Chromaturia, Cholestasis, Hepatic Enzyme Increased, Hepatocellular Damage, Liver Function Test Abnormal, Ocular Icterus, Pancreatitis, Gait Disturbance, Immobile
Adverse event resulted in: hospitalization
Suspect drug(s):
Lotrel (Amlodipine / Benazepril)
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
|