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Mononine (Coagulation Factor IX Human) - Side Effect Reports to FDA

 
 



This is an index of side effect / adverse reaction reports (a.k.a. adverse event reports) related to Mononine (Coagulation Factor IX Human) 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 (2)

Reports by Reaction Type

Epistaxis (2)

Possible Mononine side effects in 65 year old male

Reported by a physician from United States on 2012-08-24

Patient: 65 year old male, weighing 133.0 kg (292.6 pounds)

Reactions: Epistaxis

Drug(s) suspected as cause:
Benefix
    Dosage: 3000 iu, 2x/day
    Indication: Factor IX Deficiency

Mononine
    Dosage: unk
    Indication: Factor IX Deficiency
    End date: 2010-01-01

Benefix
    Dosage: 6000 iu, 2x/day (3 days)
    Start date: 2010-01-01

Benefix
    Dosage: 3000 iu, 2x/day
    Start date: 2010-01-01



Possible Mononine side effects in male

Reported by a health professional (non-physician/pharmacist) from United States on 2012-06-14

Patient: male, weighing 133.8 kg (294.4 pounds)

Reactions: Epistaxis

Drug(s) suspected as cause:
Benefix
    Dosage: 3000 iu, 2x/day
    Indication: Factor IX Deficiency

Benefix
    Dosage: 3000 iu, 2x/day
    Start date: 2010-01-01

Mononine
    Dosage: unk
    Indication: Factor IX Deficiency
    End date: 2010-01-01

Benefix
    Dosage: 6000 iu, 2x/day (3 days)
    Start date: 2010-01-01

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