Methylphenidate
(Ritalin, Ritalin SR)
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Category:
Description:
Indications:
-
Attention
deficit disorders
-
Narcolepsy
-
Depression
in elderly, cancer, and post-stroke victims (non FDA approved)
Contraindications:
-
Marked
anxiety, tension and agitation
-
Glaucoma,
Tourette’s syndrome or motor tics, prevention of normal fatigue
Precautions:
-
Pregnancy
category C
-
Severe
depression, seizure disorders, hypertension, history of drug abuse
-
Children
<6 years, symptoms associated with acute stress reactions
Adverse
Reactions (Side Effects):
-
CNS:
akathisia, dizziness, dyskinesia, fever, headache, hyperactivity,
insomnia, restlessness, talkativeness, Tourette’s syndrome (rare)
-
CV:
angina, blood pressure changes, dysrhythmias, palpitations,
tachycardia
-
GI:
abdominal pain, anorexia, dry mouth, nausea, weight loss
-
GU:
uremia
-
HEME:
anemia, leukopenia
-
METAB:
growth retardation
-
MS:
arthralgia
-
SKIN:
erythema-multiforme, exfoliative dermatitis, rash, scalp hair loss,
urticaria
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Dosage:
Administered
orally
-
Adult:
-
Child
> or =6 years:
-
Attention
deficit disorder: PO 0.3 mg/kg/dose or 2.5-5 mg/dose given
before breakfast and lunch; increase by 0.1 mg/kg/dose or 5-10mg
daily at weekly intervals; usual dose 0.5-1 mg/kg/day, max 2
mg/kg/day or 60mg daily; sustained release may be used when the 8
hour dose of sustained release corresponds to the titrated 8 hour
dose of immediate-release tablets
Drug
interactions:
-
Labs:
false positive urine amphetamine
-
MAOIs:
hypertensive reactions
-
Guanethidine:
inhibition of guanethidine antihypertensive effect
Special
considerations:
-
Overdosage
may cause vomiting, agitation, tremor, muscle twitching, seizures,
confusion, tachycardia, hypertension, arrythmias
-
Take
last daily dose prior to 1800 to avoid insomnia
-
Do
not chew or crush sustained release formulation
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Source:
Operational Medicine 2001, Health
Care in Military Settings, NAVMED P-5139, May 1, 2001, Bureau
of Medicine and Surgery, Department of the Navy, 2300 E Street NW, Washington,
D.C., 20372-5300
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