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Index of reports
> Cases resulting in other serious reactions (9)
> Cases with White Blood Cell Count Decreased (1)
Below is the selection of adverse event reports related to Lotensin (Benazepril) that includes cases resulting in other serious reactions where reactions include white blood cell count decreased.
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
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