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Factive (Gemifloxacin) - Side Effect Reports to FDA

 
 



This is an index of side effect / adverse reaction reports (a.k.a. adverse event reports) related to Factive (Gemifloxacin) and submitted to the FDA during the sample period of about a year. The information is not vetted and should not be considered as verified clinical evidence.

Reports by Event Outcome

All Cases (6)
Disability (1)

Reports by Reaction Type

Rash (3)Urticaria (2)Night Sweats (1)Hypersensitivity (1)Pruritus (1)Retinal Detachment (1)Pain (1)Visual Acuity Reduced (1)Vitreous Floaters (1)Oedema (1)Oedema Mouth (1)Sinusitis (1)

Possible Factive side effects in 53 year old male

Reported by a consumer/non-health professional from United States on 2012-06-26

Patient: 53 year old male, weighing 120.2 kg (264.4 pounds)

Reactions: Retinal Detachment, Vitreous Floaters, Visual Acuity Reduced

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Factive
    Dosage: 320 mg. 1 day for five day po
    Administration route: Oral
    Indication: Asthma
    Start date: 2007-08-21
    End date: 2007-08-25

Factive
    Dosage: 320 mg. 1 day for five day po
    Administration route: Oral
    Indication: Asthma
    Start date: 2007-12-04
    End date: 2008-01-02



Possible Factive side effects in female

Reported by a physician from Brazil on 2012-04-02

Patient: female

Reactions: Mucocutaneous Rash, Hypersensitivity, Eczema Eyelids, Oedema Mouth, Toxic Skin Eruption

Drug(s) suspected as cause:
Desloratadine
    Administration route: Oral
    Indication: Sinusitis
    Start date: 2012-03-08
    End date: 2012-03-18

Factive
    Administration route: Oral
    Indication: Sinusitis
    Start date: 2012-03-08
    End date: 2012-03-14

Desloratadine
    Administration route: Oral
    Indication: Tympanic Membrane Perforation
    Start date: 2012-03-08
    End date: 2012-03-18

Factive
    Administration route: Oral
    Indication: Tympanic Membrane Perforation
    Start date: 2012-03-08
    End date: 2012-03-14

Prelone
    Administration route: Oral
    Indication: Tympanic Membrane Perforation
    Start date: 2012-03-08
    End date: 2012-03-18

Prelone
    Administration route: Oral
    Indication: Sinusitis
    Start date: 2012-03-08
    End date: 2012-03-18



Possible Factive side effects in 45 year old female

Reported by a consumer/non-health professional from United States on 2012-02-03

Patient: 45 year old female, weighing 68.9 kg (151.7 pounds)

Reactions: Rash Generalised

Drug(s) suspected as cause:
Factive



Possible Factive side effects in male

Reported by a consumer/non-health professional from United States on 2011-12-22

Patient: male, weighing 97.5 kg (214.5 pounds)

Reactions: Urticaria, Oedema, Rash

Drug(s) suspected as cause:
Factive



Possible Factive side effects in 61 year old female

Reported by a consumer/non-health professional from United States on 2011-12-15

Patient: 61 year old female, weighing 57.2 kg (125.7 pounds)

Reactions: Night Sweats, Pruritus, Nausea, Pain, Urticaria, Rash, Gastric Disorder, Feeling Jittery, Insomnia, Sinusitis

Drug(s) suspected as cause:
Factive



Possible Factive side effects in 32 year old female

Reported by a consumer/non-health professional from United States on 2011-10-11

Patient: 32 year old female, weighing 70.3 kg (154.7 pounds)

Reactions: NO Therapeutic Response, Rash

Drug(s) suspected as cause:
Factive

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