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VPA treatment was discontinued and L-carnitine supplementation (100 mg/kg per day) was initiated
No FDA approval means the benefits and risks are unknown
Less commonly reported adverse reactions (less than 1% or less than twice rate of placebo) included increased heart rate, headache, abdominal pain upper, dyspnea, rash, insomnia, irritability, feeling jittery and anxiety
L., David, L
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The method of administration intramuscular or intravenous also affects the absorption rate and effectiveness
That leap is where expectationsand disappointmenttend to start
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