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Index of reports
> Cases resulting in life threatening events (4)
> Cases with Pharmaceutical Product Complaint (3)
Below is the selection of adverse event reports related to Proventil (Inhalation) that includes cases resulting in life threatening events where reactions include pharmaceutical product complaint.
Adverse event in 46 year old female receiving Proventil (Inhalation)
Reported by a individual with unspecified qualification from United States on 2007-10-10
Patient: 46 year old female, weighing 82.1 kg (180.6 pounds)
Adverse reactions / side effects: Asthma, Dyspnoea, Drug Ineffective, Respiratory Arrest, Pharmaceutical Product Complaint, Loss of Consciousness
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Proventil
Indication: Asthma
Proventil
Indication: Chronic Obstructive Pulmonary Disease
Proair HFA
Levalbuterol HCL
Adverse event in female receiving Proventil (Inhalation)
Reported by a consumer/non-health professional from United States on 2007-03-28
Patient: female
Adverse reactions / side effects: Dyspnoea, Pharmaceutical Product Complaint
Adverse event resulted in: life threatening event
Suspect drug(s):
Proventil (Inhalation)
Adverse event in 55 year old female receiving Proventil (Inhalation)
Reported by a consumer/non-health professional from United States on 2007-01-08
Patient: 55 year old female, weighing 59.0 kg (129.7 pounds)
Adverse reactions / side effects: Device Failure, Pharmaceutical Product Complaint
Adverse event resulted in: life threatening event
Suspect drug(s):
Proventil (Inhalation)
Other drugs received by patient: Epipen
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