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Index of reports
> Death (2)
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Vigamox (Moxifloxacin) death. The selected reports were submitted to the FDA during the sample period of about a year.
Possible Vigamox side effects in 52 year old male
Reported by a consumer/non-health professional from United States on 2012-03-28
Patient: 52 year old male, weighing 77.1 kg (169.6 pounds)
Reactions: Asthma, Dyspnoea, Throat Irritation, Wheezing, Condition Aggravated, Loss of Consciousness
Adverse event resulted in: death
Drug(s) suspected as cause:
Vigamox
Dosage: 1 drop 3x daily opthalmic 046
Indication: Cataract Operation
Prednisolone Acetate
Dosage: 1 drop 3x daily opthalmic 046
Indication: Cataract Operation
Start date: 2011-08-20
End date: 2011-09-03
Possible Vigamox side effects in 76 year old female
Reported by a consumer/non-health professional from United States on 2011-12-02
Patient: 76 year old female, weighing 52.2 kg (114.8 pounds)
Reactions: Product Substitution Issue, Urticaria, Rash Erythematous
Adverse event resulted in: death, life threatening event, hospitalization, disablity
Drug(s) suspected as cause:
Vigamox
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