Zoloft has been linked to a variety of birth defects when taken by pregnant women, including pulmonary hypertension, both cleft lip and cleft palates, heart defects, neural tube defects, cranial birth defects, anal atresia, abdominal issues and clubfoot. If you experience any side effects from your prescription, even side effects not listed; always consult your physician immediately. If you have experienced any side effects from taking Zoloft or if you took Zoloft while pregnancy, call our attorneys today or use the contact a lawyer form to the right. You may be eligible to receive compensation for any injuries or birth defects from taking Zoloft. There are several serious birth defects that can result from taking Zoloft during pregnancy and are part of the Zoloft birth defects lawsuit. Most of these defects occur from use of the drug during the 1 Trimester, but studies have shown that defects can occur in any stage of pregnancy. If you took Zoloft during pregnancy and have a child who may have one of these defects, please feel free to contact the Zoloft birth defect lawsuit immediately by clicking on the phone to the right, entering your number in the space provided and clicking again; your phone will usually ring within one minute. Your baby's birth was supposed to be one of the happiest moments of your life. Instead, your doctor informed you that your child was born with the serious birth defect of a hole in his heart. If you were prescribed Zoloft during your pregnancy (or before you even knew you were pregnant), Zoloft may be responsible for your baby's birth defect. As of October 2016, the Food and Drug Administration (FDA) has not recalled Zoloft. However, the agency has released a series of warnings about its link to serious birth defects -- including feeding issues and abdominal organs poking through a newborn's belly button -- and serious side effects. Unfortunately, those warnings came too late for many moms who took the drug. Read about the first steps to possibly being reimbursed for your child's injuries through a Zoloft lawsuit and the kinds of damages (monetary compensation) you might be awarded. Zoloft is a prescription drug used to treat severe depression and a variety of other conditions, including anxiety, obsessive compulsive disorder (OCD), post-traumatic stress disorder (PTSD), and premenstrual dysphoric disorder. How do you buy cialis online Where to buy retin a in sydney See risks & benefits. Learn more about ZOLOFT® sertraline HCl, a prescription treatment for depression. Jan 12, 2018. Pfizer Inc. is recalling 30-count bottles of 25-mg Zoloft sertraline hydrochloride tablets NDC 0049-4960-30, according to the January 10. Oct 26, 2015. Usage, warnings, side effects, and community information for the prescription drug Zoloft. Most common adverse reactions (≥5% and twice placebo) in pooled placebo-controlled MDD, OCD, PD, PTSD, SAD and PMDD clinical trials were nausea, diarrhea/loose stool, tremor, dyspepsia, decreased appetite, hyperhidrosis, ejaculation failure, and decreased libido (6.1) At least 14 days must elapse between discontinuation of a monoamine oxidase inhibitor (MAOI) antidepressant and initiation of sertraline hydrochloride. In addition, at least 14 days must elapse after stopping sertraline hydrochloride before starting an MAOI antidepressant Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. The data described below are from randomized, double-blind, placebo-controlled trials of sertraline hydrochloride (mostly 50 mg to 200 mg per day) in 3066 adults diagnosed with MDD, OCD, PD, PTSD, SAD, and PMDD. These 3066 patients exposed to sertraline hydrochloride for 8 to12 weeks represent 568 patient-years of exposure. The mean age was 40 years; 57% were females and 43% were males. The most common adverse reactions (≥5% and twice placebo) in all pooled placebo-controlled clinical trials of all sertraline hydrochloride-treated patients with MDD, OCD, PD, PTSD, SAD and PMDD were nausea, diarrhea/loose stool, tremor, dyspepsia, decreased appetite, hyperhidrosis, ejaculation failure, and decreased libido (see Table 3). The following are the most common adverse reactions in trials of sertraline hydrochloride (≥5% and twice placebo) by indication that were not mentioned previously. is recalling 30-count bottles of 25-mg Zoloft (sertraline hydrochloride) tablets (NDC 0049-4960-30), according to the January 10, 2018, US Food and Drug Administration (FDA) Enforcement Report. The company cited weight variations in the tablets that have caused superpotent and subpotent drugs. The recall affects 1972 bottles of Zoloft from lot S84026. The bottles were distributed across the United States by Pfizer’s Roerig division. Pfizer voluntarily initiated the recall October 20, 2017. On January 4, 2018, the FDA designated it Class II, signaling use of the prescription drug could cause temporary, reversible adverse effects with a remote likelihood of serious harm. Zoloft is a selective serotonin reuptake inhibitor used in the treatment of depression, obsessive-compulsive disorder, posttraumatic stress disorder, premenstrual dysphoric disorder, social anxiety disorder, and panic disorder. Sertraline recall Zoloft Overview Recall Report, Recall Depression Drug Population Health Learning Network Sertraline dosage formsTamoxifen preventionErectafil 20 PDF This study investigated the cognitive side effects of a 6-week course of sertraline treatment on verbal memory and attention in children and adolescents. The Influence of Sertraline on Attention and Verbal Memory in.. Zoloft sertraline hydrochloride Recall, Side Effects & Warnings. Many People Taking Antidepressants Discover They Cannot Quit.. Information provided by pilot to provide Human Drug recall information before it has been. Sertraline HCl Tablets, 25 mg, 30 count bottles, Rx. Drug recalls are actions taken by a firm to remove a product from the market and may. A recall is a voluntary action taken by a company at any time to remove a. October 2016, the Food and Drug Administration FDA has not recalled Zoloft. other companies sell a generic version of the drug sertraline hydrochloride.