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Vigamox (Moxifloxacin) - Death - Suspected Cause - Side Effect Reports

 
 



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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