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

 
 



Index of reports > Disability (3)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Vigamox (Moxifloxacin) disability. The selected reports were submitted to the FDA during the sample period of about a year.

Possible Vigamox side effects in 65 year old female

Reported by a health professional (non-physician/pharmacist) from United States on 2012-04-20

Patient: 65 year old female, weighing 58.1 kg (127.7 pounds)

Reactions: Endophthalmitis, Post Procedural Complication

Adverse event resulted in: disablity

Drug(s) suspected as cause:
BSS
    Dosage: intraocular
    Indication: Intraocular Lens Implant
    Start date: 2012-02-16
    End date: 2012-02-16

Vigamox
    Dosage: ophthalmic
    Indication: Preoperative Care
    Start date: 2012-01-01

Other drugs received by patient: Epinephrine



Possible Vigamox side effects in 77 year old male

Reported by a health professional (non-physician/pharmacist) from United States on 2012-03-27

Patient: 77 year old male, weighing 88.5 kg (194.6 pounds)

Reactions: Endophthalmitis, Medication Error, Eye Infection Bacterial, Visual Acuity Reduced, Streptococcal Infection, Treatment Noncompliance

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Vigamox
    Dosage: (ophthalmic)
    Indication: Intraocular Lens Implant
    Start date: 2011-12-21
    End date: 2011-12-21

Betadine
    Dosage: (ophthalmic)
    Indication: Intraocular Lens Implant
    Start date: 2011-12-21
    End date: 2011-12-21

BSS
    Dosage: (intraocular)
    Indication: Intraocular Lens Implant
    Start date: 2011-12-21
    End date: 2011-12-21

Other drugs received by patient: Epinephrine; Cefuroxime



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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