Cital- opram, escitalopram, venlafaxine, duloxetine, and mirtazapine are the least likely to have drug-drug interactions; sertraline is likely, and fluoxetine, fluvoxamine, paroxetine, and all the tricyclic antidepressants are very likely to interact with other drugs cancer patients are taking.
Read about Paroxetine.
Drug interactions may change how your medications work or increase your risk for serious side effects. This document does not contain all possible drug interactions. Keep a list of all the products you use (including prescription/nonprescription drugs and herbal products) and share it with your doctor and pharmacist. Do paroxetine online start.stop.or change the dosage of any medicines without your doctor’s approval.
Do not use an MAO inhibitor within 14 days before or 14 days after you take paroxetine. A dangerous drug interaction could occur. MAO inhibitors include isocarboxazid.linezolid.phenelzine.rasagiline.selegiline.and tranylcypromine. After you stop paroxetine online paroxetine you must wait at least 14 days before you start taking an MAO inhibitor.
Hemic and Lymphatic Systems. Infrequent. Anemia.leukopenia.lymphadenopathy.purpura. rare. Abnormal erythrocytes.basophilia.bleeding time increased.eosinophilia.hypochromic anemia.iron deficiency anemia.leukocytosis.lymphedema.abnormal lymphocytes.lymphocytosis.microcytic anemia.monocytosis.normocytic anemia.thrombocythemia.thrombocytopenia.
3. “Product Information. Paxil CR (paroxetine).” SmithKline Beecham.Philadelphia.PA.
Such combinations may lead to confusion.high blood pressure.tremor.hyperactivity.coma.and death. (A period of 14 days without treatment should lapse when switching between paroxetine and MAOIs.) Similar reactions occur when paroxetine is combined with other drugs for example.tryptophan.St. John’s wort.meperidine (Demerol).tramadol (Ultram) that increase serotonin in the brain.
Long-term maintenance of efficacy was demonstrated in a 3-month relapse prevention trial. In this trial.patients with panic disorder assigned to paroxetine demonstrated a lower relapse rate compared to patients on placebo (see Clinical Trials ). Panic disorder is a chronic condition.and it is reasonable to consider continuation for a responding patient. Dosage adjustments should be made to maintain the patient on the lowest effective dosage.and patients should be periodically reassessed to determine the need for continued treatment.
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