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Kogenate (Antihemophilic Factor) - Haemarthrosis - Suspected Cause - Side Effect Reports

 
 



Index of reports > Cases with Haemarthrosis (3)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Kogenate (Antihemophilic Factor) where reactions include haemarthrosis. The selected reports were submitted to the FDA during the sample period of about a year.

Possible Kogenate side effects in 43 year old male

Reported by a pharmacist from United States on 2012-06-12

Patient: 43 year old male, weighing 45.4 kg (99.8 pounds)

Reactions: Haemarthrosis, Haemorrhage, Factor Viii Inhibition

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Kogenate

Kogenate

Kogenate
    Dosage: 4-6 units/kg/hr continuous infusio iv drip
    Indication: Haemorrhage
    Start date: 2011-10-10
    End date: 2011-10-14

Kogenate
    Dosage: 4 units/kg/hr continuous infusio iv drip
    Indication: Haemorrhage
    Start date: 2011-06-27
    End date: 2011-06-30

Other drugs received by patient: Advate



Possible Kogenate side effects in 69 year old male

Reported by a pharmacist from United States on 2012-06-08

Patient: 69 year old male, weighing 88.0 kg (193.6 pounds)

Reactions: Product Quality Issue, Haemorrhage, Haemarthrosis, Haematuria, Coronary Artery Disease, Factor Viii Inhibition, Weight Bearing Difficulty, NO Therapeutic Response, Chest Pain

Adverse event resulted in: life threatening event, hospitalization, disablity

Drug(s) suspected as cause:
Kogenate
    Dosage: 4-5units/kg/hr continuous infusion iv drip
    Indication: Factor Viii Deficiency
    Start date: 2012-02-08
    End date: 2012-02-14

Kogenate
    Dosage: 4-5units/kg/hr continuous infusion iv drip
    Indication: Haemorrhage
    Start date: 2012-02-08
    End date: 2012-02-14

Kogenate
    Dosage: 6units/kg/hr continuous infusion iv drip
    Start date: 2012-03-01
    End date: 2012-03-02



Possible Kogenate side effects in 23 year old male

Reported by a pharmacist from United States on 2012-06-08

Patient: 23 year old male, weighing 75.0 kg (165.0 pounds)

Reactions: Product Quality Issue, Therapeutic Response Decreased, Haemarthrosis, Factor Viii Inhibition

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Kogenate
    Dosage: 4-5 units/kg/hr continuous infusion iv drip
    Start date: 2012-04-06
    End date: 2012-04-10

Kogenate
    Dosage: 4 units/kg/hr continuous infusion iv drip
    Indication: Factor Viii Deficiency
    Start date: 2012-03-11
    End date: 2012-03-14

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