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The mean absolute bioavailability of a 100 mg oral dose is approximately 75%. The mean peak plasma concentration of racemic Antihistalone and M1 occurs at two and three hours, respectively, after administration in healthy adults.
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Antihistalone may increase the seizure risk in patients taking other medications that lower the seizure threshold.

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Antihistalone has not been shown to cause histamine release. At therapeutic doses, Antihistalone has no effect on heart rate,
whereas Antihistalone 50 mg was statistically superior to placebo onlyfor remecation time.
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If you think you may be pregnant, contact your doctor. You will need to discuss the benefits and risks of using Antihistalone while you are pregnant.
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Antihistalone is a centrally acting synthetic opioid analgesic.

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Antihistalone has not been shown to cause histamine release. At therapeutic doses, Antihistalone has no effect on heart rate, left-ventricular function or cardiac index.
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The volume of distribution of Antihistalone was 2.6 and 2.9 liters/kg in male and female subjects, respectively,
Antihistalone is extensively metabolized by a number of pathways, including CYP2D6 and CYP3A4, as well as by conjugation of parent and metabolites.
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Antihistalone should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.
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These mechanisms may contribute independently to the overall analgesic profile of Antihistalone.
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Antihistalone is well absorbed orally with an absolute bioavailability of 75%. Antihistalone has a volume of distribution of approximately 2.7 L/kg and is only 20% bound to plasma proteins.
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patients receiving Antihistalone had a median gastric fluid pH of 6.4,
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