FELBA VH*
    
Manufacturer Details
    BAXTER INC
    
    
    
    
    
 
      
Compositions:
Anti-Inhibitor Coagulant Complex  8mg/ml freeze-dried anti-inhibitor coagulant complex  in vials with diluent and needles  ,
  
 
 
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      Strength
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      Rate
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      Packing Style
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            8mg/ml fd.complx
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            0.00
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            in vials with diluent and needles
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List of Related Indications:
List Of Drugs:
   - Anti-Inhibitor Coagulant Complex- @- Antihemophilic Agents
 
 
Indication Type Description:
    
    
    
    
           
            Adverse Reaction:
        
        
            
	Allergic -  allergic reactions ranging from mild to short-term urticarial rashes to severe anaphylactoid
	reactions. discontinue immediately if such signs appear.
	Cardiovascular-   thromboembolic reactions may occur particularly after high doses or in patients
	with thrombotic risk factors.
        
     
    
    
           
            Contra-Indications:
        
        
            
	
	Special Precautions-
	Potential disease transmission-   AICC is made from human plasma . Products made from plasma
	may contain infectious agents such as viruses, that can cause disease. The risk can be reduced by
	effetive screening of the donor , testing for infectious agents
	Idenification of clotting deficiency- use AICC only in patients with circulating inhibitors to one or more
	coagulation factors and do not use it for the treatment of bleeding episodes resulting from coagulation
	factor deficiency. Do not give it to patients with significant signs of disseminated intravascular
	coagulation DIC or fibronolysis
	High doses - give high doses of AICC only as long as absolutely necessary to stop bleeding
	Concomittant antifibrinolytics- it has  been reported that AICC and antifibronolytics have been given
	simultaneously without complications. It is however, recommended not to use antifibrinolysis until
	12 hours after the administration of AICC.
	Anamnestic response- anamnestic responses with rises in factor VIII  inhibitor titer have been
	observed in 20% of the cases.
	Viral infections- individuals who receive infusions of blood or plasma products may develop
	signs and/or symptoms of some viral infections, paricularly non-A , non-B hepatitis
	Pregnancy- not known whether AICC can cause fetal harm when administered to a pregnant woman.
	Give to a pregnant woman only if required
	Children-  no data  are available regarding use of AICC in children
	Monitoring- monitor patients receiving AICC 100units/kg of body weight for the development of
	DIC and/or symptoms of acute coronary ischemia.
	
	 
        
     
    
    
           
            Dosages/ Overdosage  Etc:
        
        
            
	Indication-
	Hemorrhage
	Dosage-
	Recommended dosage- as  general gideline a dosage range of 50 to 100 units of AICC per kg of body
	weight is recommended.
        
     
    
    
           
            Patient Information:
        
        
            
	1. Some viruses such as paraviris B19 or hepatitis A are particularly difficult to remove or
	    inactivate at this time.
	2. Paravirus B19 most seriously affect pregnant woman or immune-compromised individuals
	3. Symptoms of paravirus B19 include fever, drowsiness, chills, and runny nose followed by
	    2 weeks later by a rash and joint pain.
	4. Evidence of hepatitis A several days or weeks of poor appetite, tiredness, and low grade
	    fever, followed by nausea, vomiting, and pain in the belly. Dark urine and yellow complexion
	    are also common  symptoms.
	5. Encourage patients to consult their health care provider if such symptoms develop.
        
     
    
    
           
            Pregnancy and lactation:
        
        
            
	Pregnancy-
	Not known whether AICC can cause fetal harm when administered to a pregnant woman.
	Give to a pregnant woman only if required
	Children- 
	No data  are available regarding use of AICC in children