|
Index of reports
> Cases resulting in other serious reactions (67)
> Cases with Dizziness (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 dizziness.
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 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 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
|
