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Lotrel (Amlodipine / Benazepril) - Adverse Event Reports - Life Threatening Events - Pleurisy

 



Index of reports > Cases resulting in life threatening events (4) > Cases with Pleurisy (1)

Below is the selection of adverse event reports related to Lotrel (Amlodipine / Benazepril) that includes cases resulting in life threatening events where reactions include pleurisy.

Adverse event in 65 year old male receiving Lotrel (Amlodipine / Benazepril)

Reported by a physician from United States on 2007-04-25

Patient: 65 year old male, weighing 109.5 kg (240.9 pounds)

Adverse reactions / side effects: LIP Swelling, Angioedema, Dyspnoea, Respiratory Disorder, Gout, Drug Hypersensitivity, Lens Implant, Pleurisy, Urticaria, Swollen Tongue

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Lotrel
    Dosage: level 3
    Administration route: Oral
    Indication: Hypertension
    Start date: 2005-06-28
    End date: 2006-03-28

Lotrel
    Dosage: level 1
    Administration route: Oral
    Start date: 2005-05-02
    End date: 2005-06-02

Lotrel
    Dosage: level 2
    Administration route: Oral
    Start date: 2005-06-03
    End date: 2005-06-27

Cosopt

Ketorolac Tromethamine

Allopurinol
    Dosage: 300 mg, unk
    Administration route: Oral

Ofloxacin

Prednisolone

Other drugs received by patient: Aspirin; Avandia; Darvon-N; Hydrocodone; Acetaminophen; NPH Insulin; Insulin; Lasix; Metoprolol Succinate; Neurontin; Montelukast Sodium; Nitroglycerin; Simvastatin

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