This drug is metabolized by a specific set of liver enzyme. Several other drugs interfere with these liver enzymes, and thus, may increase or decrease the clearance of bupropion from the body,
potentially increasing the risk of side effects or decreasing effectiveness. When these drugs are given in combination with bupropion, dosage adjustments may be needed. As these are too numerous to list, you
should always check with your doctor or pharmacist prior to starting a new medication, herbal, or nonprescription product.
PREGNANCY AND BREAST-FEEDING CAUTIONS
FDA Pregnancy Risk Category B. This drug is excreted in breast milk. Breast-feeding is not recommended during therapy with this drug.
SPECIAL INFORMATION
Do not use Zyban and Wellbutrin concurrently, as they contain the same active ingredient.
Take immediate release formulations in equally divided doses (three or four times daily) to avoid risk of seizures. Do not chew or crush the XL or SR formulations. The bupropion XL formulation may be excreted in the stool.
This is an empty shell which is not absorbed. The drug has been absorbed. This drug may cause significant sedation and drowsiness, which may impair your ability to perform tasks requiring judgment
or motor or cognitive skills. If you experience a seizure while on this medication, stop immediately and report it to your doctor.
In January 2005, the FDA announced new labeling for antidepressants regarding the need to closely monitor for worsening of depression and for the potential of increased suicidal
thinking or suicide behavior during therapy. Although this recommendation applies to all patients (adults, children, and adolescents) treated with antidepressants for any indication, this is of particular importance if you are being treated for depression.