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FDA Issues Approvable Letter For RISPERDAL(R) To Treat Adolescents With Schizophrenia And Children And Adolescents With Bipolar Mania
Johnson & Johnson 
Pharmaceutical Research & Development, L.L.C. (J&JPRD) announced it has  
received an approvable letter from the U.S. Food and Drug Administration 
(FDA) regarding two supplemental New Drug Applications (sNDA) for 
RISPERDAL(R) (risperidone), filed on Dec. 21, 2006. The sNDAs are for the 
treatment of schizophrenia in adolescents ages 13-17 years and for the 
short-term treatment of bipolar mania associated with bipolar I disorder in 
children and adolescents ages 10-17 years, respectively. The FDA has not 
asked for any additional studies. J&JPRD is currently reviewing the 
approvable letter and looks forward to finalizing the label with the 
agency.
 
Important Safety Information For RISPERDAL(R)
 
    
Elderly Patients with dementia-related psychosis treated with atypical 
antipsychotic drugs are at an increased risk of death compared to placebo. 
RISPERDAL(R) (risperidone) is not approved for the treatment of patients 
with Dementia-Related Psychosis.
 
    
Schizophrenia: The most common side effects that occurred with 
RISPERDAL(R) were anxiety, sleepiness, restlessness, tremors and muscle   
stiffness; dizziness, constipation, nausea, indigestion, runny nose, rash 
and rapid heartbeat.
 
    
Bipolar Mania: The most common side effects that occurred in clinical  
trials with RISPERDAL(R), in the treatment of bipolar mania either alone or 
in combination with a mood stabilizer (lithium or valproate) were: 
sleepiness, muscle stiffness, restlessness, tremor, indigestion, nausea, 
abnormal vision, muscle aches, dizziness, runny nose, diarrhea, increased 
saliva, stomach pain and urinary incontinence.
 
    
Autistic Disorder: The most common side effects that occurred with  
RISPERDAL(R) were sleepiness, increased appetite, fatigue, upper 
respiratory tract infection, increased saliva, constipation, dry mouth, 
tremor, muscle stiffness, dizziness, repetitive behavior, involuntary 
movement, rapid heartbeats, confusion, weight increase.
 
    
A rare but serious side effect that has been reported with this kind of 
medicine, including RISPERDAL(R), is known as neuroleptic malignant 
syndrome (NMS). NMS is characterized by muscle rigidity, fever and can be     
serious.
 
    
You may have heard the term "tardive dyskinesia." These are usually 
persistent, uncontrollable, slow or jerky facial or body movements that can   
be caused by all medications of this type. If you have these symptoms, talk 
to your health care professional.
 
    
Studies suggest an increased risk of elevated blood sugar-related side 
effects, and sometimes potentially fatal, in patients treated with this 
class of medications, including RISPERDAL(R). Some people may need regular  
blood sugar testing.
 
    
Some people taking RISPERDAL(R) may feel faint or lightheaded when they  
stand up or sit up too quickly. By standing up or sitting up slowly and 
following your health care professional's dosing instructions, this side 
effect may be reduced or it may go away over time.
 
    
You may have heard the term "extrapyramidal symptoms" (EPS). These are 
usually persistent movement disorders or muscle disturbances, such as 
restlessness, tremors and muscle stiffness. Some people taking RISPERDAL(R)  
have these side effects. If you have these symptoms, talk to your health 
care professional.
 
    
Some medications may interact with RISPERDAL(R). Avoid alcohol while on  
RISPERDAL(R).
 
    
Inform your health care professional if you are pregnant or if you are 
planning to get pregnant while taking RISPERDAL(R). Do not breastfeed if   
you are taking RISPERDAL(R).
 
    
RISPERDAL(R) may affect your driving ability, therefore, do not drive   
or operate machines before talking to your health care professional.
 
    
RISPERDAL(R) may affect alertness and motor skills; use caution until 
the effect of RISPERDAL(R) is known.
 
    
Please see full important U.S. prescribing information for RISPERDAL(R) 
at http://www.janssen.com.
 
    
Janssen, L.P., based in Titusville, NJ, is the only pharmaceutical 
company in the U.S. dedicated solely to mental health. The company    
currently markets prescription medications for the treatment of 
schizophrenia, bipolar mania and irritability associated with autistic 
disorder. For more information about Janssen, L.P., visit http://www.janssen.com, 
and for more information on RISPERDAL(R), visit http://www.RISPERDAL.com.
 
   
 
Johnson & Johnson Pharmaceutical Research and Development, L.L.C., is  
headquartered in Raritan, NJ, and has facilities throughout Europe and the 
U.S. The company is leveraging drug discovery and drug development in a 
variety of therapeutic areas to address unmet medical needs worldwide.
 
Johnson & Johnson Pharmaceutical Research and Development,L.L.C.
http://www.janssen.com
View drug information on Risperdal Oral Formulation.
		
FDA probleme Approvable scrisoare pentru RISPERDAL (R) pentru a trata schizofrenia cu adolescenþi ºi copii ºi adolescenþi cu bipolar Mania - FDA Issues Approvable Letter For RISPERDAL(R) To Treat Adolescents With Schizophrenia And Children And Adolescents With Bipolar Mania - articole medicale engleza - startsanatate