venlafaxine in A Sentence

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    Amitriptyline and Venlafaxine are probably also effective.

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    Venlafaxine: how and when to use.

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    Of Venlafaxine and 30% of EFA are associated with plasma proteins.

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    The half-lives of Venlafaxine and EFA are, respectively, 5 and 11 hours.

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    Venlafaxine has no affinity for M-cholinergic receptors, H-1 histamine and α-1 adrenergic receptors.

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    The example of a drug of this type available at present is Venlafaxine.

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    Venlafaxine is cleaved in the liver with the formation of an active metabolite- O-desmethylVenlafaxine(EFA).

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    Hours after taking the tablets, the maximum concentration of Venlafaxine in the blood plasma is reached.

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    9

    With repeated use, a stable concentration of Venlafaxine and metabolite in the plasma is achieved for 3 days.

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    Combination with diazepam, risperidone does not cause a change in the therapeutic effect of these drugs and Venlafaxine;

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    11

    There is no evidence regarding the safety of Venlafaxine in pregnant women, so the drug is contraindicated during pregnancy.

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    12

    Venlafaxine does not have an affinity for M-cholinergic receptors, H-cholinergic receptors, H-1 histamine-receptors, and α-1 adrenergic receptors of the brain.

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    13

    In patients with cirrhosis of the liver, the concentration of Venlafaxine and EFA in the blood plasma increases, and the rate of excretion decreases;

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    14

    Because for most people the metabolite accounts for about two-thirds of the amount of medication in the bloodstream, ODV is thought to primarily account for the therapeutic activity of Venlafaxine.

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    15

    Venlafaxine is well absorbed from the digestive tract. The maximum concentration of the active substance in the blood is observed 2.4 hours after the drug administration, the maximum concentration of the active metabolite is 4.3 hours.

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