effexor xr interactions

Common side effects of Effexor include nausea, headaches, anxiety, insomnia, drowsiness, loss of appetite, dizziness, ejaculation disorder, sweating, dry mouth, and weight … ©2020 Pfizer. {* registrationNewVerificationTitle *}



{* traditionalSignIn_emailAddress *} In common with SSRI’s, pharmacodynamic interactions between EFFEXOR XR and the herbal remedy St. John’s Wort may occur and may result in an increase in undesirable effects. Effexor XR is an extended-release capsule for once-a-day oral administration that contains venlafaxine hydrochloride, a serotonin and norepinephrine reuptake inhibitor (SNRI). Individual plans may vary Immediate release 75 mg/day PO divided q8-12hr initially; may be increased by ≤75 mg/day not faster than every 4 days Moderate: Up to 225 mg/day PO divided q8-12hr Severe: Up to 375 mg/day PO divided q8-12hr {* acknowledgement_consent *} Find patient medical information for Effexor XR Oral on WebMD including its uses, side effects and safety, interactions, pictures, warnings and user ratings. 2002

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Please confirm that you would like to log out of Medscape. {* acknowledgement_consent *} Drinking alcohol with this medicine can cause side effects. 1859039-overview Common side effects of Effexor include nausea, headaches, anxiety, insomnia, drowsiness, loss of appetite, dizziness, ejaculation disorder, sweating, dry mouth, and weight loss.

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La venlafaxine n’a pas de forte liaison aux protéines plasmatiques.


The study is created by eHealthMe based on reports of 435 people who take Zyrtec and Effexor xr from the FDA, and is updated regularly. All material on this website is protected by copyright, Copyright © 1994-2020 by WebMD LLC.

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These medications are not usually taken together.




"Bicyclic" antidepressant; drug is structurally unrelated to SSRIs, MAOIs, and tricyclic antidepressants (TCAs), but it and its metabolite are potent inhibitors of serotonin and norepinephrine reuptake and weak inhibitors of dopamine reuptake; it does not have MAOI activity or activity for H1 histaminergic, muscarinic cholinergic, or alpha2-adrenergic receptorsPeak plasma time: 2-3 hr (immediate release); 5.5-9 hr (extended release)Concentration: Immediate release, 225-290 ng/mL; extended release, 150-260 ng/mLHalf-life: 5-11 hr (prolonged in renal or hepatic dysfunction)Adding plans allows you to compare formulary status to other drugs in the same class.To view formulary information first create a list of plans.

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