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Perforomist (Formoterol Inhalation) - Disability - Suspected Cause - Side Effect Reports

 
 



Index of reports > Disability (1)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Perforomist (Formoterol Inhalation) disability. The selected reports were submitted to the FDA during the sample period of about a year.

Possible Perforomist side effects in 60 year old female

Reported by a individual with unspecified qualification from United States on 2012-06-07

Patient: 60 year old female, weighing 65.8 kg (144.7 pounds)

Reactions: Paranasal Sinus Discomfort, Wheezing, Rhinorrhoea, Ocular Discomfort, Lacrimation Increased, Nasal Septum Perforation, Epistaxis

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Perforomist
    Dosage: 20mcg/2ml vial, twice daily, in nebulizer
    Indication: Chronic Obstructive Pulmonary Disease
    Start date: 2011-06-01
    End date: 2012-01-01

Perforomist
    Dosage: 20mcg/2ml vial, twice daily, in nebulizer
    Indication: Dyspnoea
    Start date: 2011-06-01
    End date: 2012-01-01

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