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The analgesic activity of Amantadine is due to both parent drug and the M1 metabolite (see CLINICAL PHARMACOLOGY, Pharmacodynamics).
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Amantadine has not been shown to cause histamine release. At therapeutic doses, Amantadine has no effect on heart rate,
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Talk with your doctor if Amantadine stops working well. Do not take more than prescribed.Some people who use Amantadine for a long time without a break may develop a physical need to continue taking it.
more potent than Amantadine in producing analgesia and 200 times more potent in ?-opioid binding.
Amantadine has not been shown to cause histamine release. At therapeutic doses, Amantadine has no effect on heart rate,
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whereas Amantadine 50 mg was statistically superior to placebo onlyfor remecation time.
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Amantadine and M1 elimination half-lives (13 hrs. for Amantadine and 19 hrs. for M1).
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the rates of withdrawals due to adverse events appeared to be higher in the Amantadine groups.
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Amantadine can increase the risk of seizure in epileptic patients, especially with simultaneous use of tricyclic antidepressants,
It is slightly soluble in water and freely soluble in alcohol,
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This indicates that Amantadine slightly decreases the precision of thermoregulatory control in addition to reducing the setpoint.
Prepare for the withdrawal symptoms of discontinued Amantadine use.

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