FDA Classifies Paxil as a Category D Medicine
Paxil, or paroxetine, is an antidepressant that has been known to cause severe birth defects if taken during pregnancy. The FDA classifies Paxil as a Category D medicine, indicating the level of risk to unborn children. Category D medicines can be given to pregnant women, if the benefits of the drug outweigh the possible risks to the fetus. In the case of Paxil, if a woman is unresponsive to other antidepressants and suffers acute depression, the drug may be prescribed.
Still Paxil poses a prominent risk to babies if mothers take the drug during pregnancy. If taken in early pregnancy, the drug denotes possible heart problems to the fetus and mother ranging from mild to severe and may require surgery. Paxil is also known to cause persistent pulmonary hypertension (PPHN), a condition that affects newborns’ circulation and breathing patterns, preventing oxygen from the heart and lungs. PPHN can be fatal or cause permanent damage to the baby. Paxil can be found in breast milk and can be harmful to feeding babies.
Paxil, as well as other selective serotonin reuptake inhibitors (SSRIs), may include further side effects if abruptly discontinued. It is better to gradually ease off the drug in accordance with a physician’s recommendation. If taking Paxil has injured you or someone you love, consult an experienced product liability attorney to discuss a claim. Manufacturers may be held responsible for defective products and you may be entitled to compensation. Call (866) 620-5757 to speak with an experienced Missouri personal injury lawyer at Page Cagle. We will help answer any product liability and personal injury questions that you may have.
