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Lotrel (Amlodipine / Benazepril) - Adverse Event Reports - Other Serious Reactions - Abdominal Pain

 



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

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