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Index of reports
> Cases resulting in a serious event (4)
> Cases with Wrong Technique in Drug Usage Process (1)
Below is the selection of adverse event reports related to Flovent HFA (Fluticasone Inhalation) that includes cases resulting in a serious event where reactions include wrong technique in drug usage process.
Adverse event in 61 year old female receiving Flovent HFA (Fluticasone Inhalation)
Reported by a consumer/non-health professional from United States on 2007-07-23
Patient: 61 year old female, weighing 65.8 kg (144.7 pounds)
Adverse reactions / side effects: Drug Effect Decreased, Wrong Technique in Drug Usage Process, Wheezing, Bronchitis, Pharmaceutical Product Complaint
Suspect drug(s):
Proair HFA
Dosage: 2 puffs 4 times a day inhal
Indication: Asthma
Start date: 2007-07-10
End date: 2007-07-22
Flovent HFA
Dosage: 2 puffs 2 times a day inhal
Indication: Bronchitis
Start date: 2007-07-10
End date: 2007-07-22
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