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Index of reports
> Disability (2)
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Atrovent (Ipratropium) disability. The selected reports were submitted to the FDA during the sample period of about a year.
Possible Atrovent side effects in female
Reported by a consumer/non-health professional from Brazil on 2012-06-20
Patient: female
Reactions: Fatigue, Dyspnoea, Chronic Obstructive Pulmonary Disease
Adverse event resulted in: disablity
Drug(s) suspected as cause:
Atrovent
Dosage: 0.5 mg
Indication: Chronic Obstructive Pulmonary Disease
Start date: 2008-01-01
Berotec
Dosage: 7.5 mg
Indication: Chronic Obstructive Pulmonary Disease
Start date: 2008-01-01
Other drugs received by patient: Alenia
Possible Atrovent side effects in female
Reported by a pharmacist from France on 2012-06-15
Patient: female, weighing 65.0 kg (143.0 pounds)
Reactions: Ageusia, Anosmia
Adverse event resulted in: disablity
Drug(s) suspected as cause:
Atrovent
Other drugs received by patient: Amoxicillin and Clavulanate Potassium; Prednisolone; Bricanyl; Oxygenotherapy
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