Case Study Suggests Even Low-Dose Risperdal Side Effects May Cause Tardive Dyskinesia Movement Disorders
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Bard PowerPort Lawsuit Serious and life-threatening injuries have been linked to problems with Bard PowerPort. Lawsuits are now being pursued by individuals who suffered injuries from the implantable port catheter fracturing or migrating.
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Antipsychotic Prescribing Guidelines For Children Often Not Followed By Doctors: Report October 10, 2014 Irvin Jackson Add Your CommentsIt appears that doctors may only follow recommended guidelines for prescribing powerful antipsychotics like Risperdal and Abilifyย to children about half the time, according to a recent hearing involving practices by Vermont physicians.Late last month, the Vermont State Legislature’s Mental Health Oversight Committee held a hearing on doctor practices in that state involving the use of antipsychotic medications among children.During the hearing, testimony given by Dr. David C. Rettewย (PDF), Director of the Pediatric Psychiatry Clinic at University of Vermont’s College of Medicine, indicated that while rates of antipsychotic prescriptions to children in that state were dropping, doctors only followed prescribing guidelines by the American Academy of Child and Adolescent Psychiatry (AACAP) about 51% of the time.Do You Know about…Spinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONDo You Know AboutโฆSpinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONRettew told legislators that a recent survey revealed that doctors in that state followed FDA recommendations on giving antipsychotics to children even less often; only 27% of the time. He did not say how those numbers compared with other states, but there was no indication of any particular factors which would make the prescribing of powerful psychotropic drugs to minors in Vermont different from most other states.“The main reason best practice guidelines were not followed was much more related to a lack of labwork monitoring rather than prescribing these medications for mild problems or before other pharmacological and nonpharmacological treatments had been tried first,” Rettew testified to members of the state legislature.That would suggest that it is not a problem of prescribing the wrong drugs to children so much as it is not following up properly on children they have told to take these medications.However, Rettew also found that only 15% of children received “evidence-based” psychotherapy before being prescribed antipsychotic drugs. He also reported that in many cases the prescriber currently responsible for a child’s antipsychotic use was not the person who originally prescribed the drug and that there was often a lack of knowledge of child patients’ prior treatment history.Childhood Antipsychotic ConcernsThe report comes about a year after the Department of Health and Human Services’ Office of the Inspector General (DHHS-OIG) launched an investigation into the use of antipsychotic drug prescriptions and use by recipients of Medicaid under the age of 18.Both older antipsychotics and newer atypical antipsychotics are included in the investigation. Some of those drugs have actually been approved for treatment of children with behavior disorders, such as bipolar and schizophrenia, while others are often prescribed โoff-labelโ by doctors, for indications that have not been approved by the FDA as safe and effective.Doctors and parents have raised concerns that the drugs are being overused to treat behavioral problems, unnecessarily exposing children to the risk of side effects from antipsychotics.In many cases, critics indicate that the focus should be on working with the child and his or her caregivers in order to determine the cause of their behavior.In 2012, a study published in the medical journal Archives of General Psychiatry found that children are prescribed antipsychotics at a higher rate than adults, with use of those drugs by children increasing at a more rapid rate than by adults from 2003 through 2009. The report found that one-in-three minors that go to see a psychiatrist are prescribed an antipsychotic to address their behavior.Studies regarding the effectsย of such drugs for children, especially when prescribed for unapproved uses, have been found to cause weight gain and to also quadruple the risk of developing diabetes in children under the age of 18.While all atypical antipsychotic medications have been associated with a potential increased risk of childhood diabetes, a growing number of Abilify lawsuits are being pursued by families of individuals who used this popular medication, with complaints suggesting that the average dose of the medication may increase a child’s risk of diabetes 7.72 percent above normal.Concerns have also been raised in recent years about a potential link between Johnson & Johnson’s atypical antipsychotic Risperdal and male breast growth seen among boys and young adults who used the drug. Known as gynecomastia, use of Risperdal has been linked to the irreversible development of breasts among boys, which can cause a serious impact on the child’s quality of life and may result in the need for surgical breast removal.Hundreds ofย Risperdal breast growth lawsuitsย are pending in courts throughout the country, which allege that the drug maker failed to adequately warn users or the medical community about the risk of boys developing breasts following use of the medication. These problem are often misdiagnosed as weight gain associated with the medication, but in some cases boys have developed breasts measuring as large as a 38D cup size after using the medication.Additional studies have also identified other potentialย side effects of atypical antipsychotics, including a potential risk of urinary problems and even death. Written by: Irvin JacksonSenior Legal Journalist & Contributing EditorIrvin Jackson is a senior investigative reporter at AboutLawsuits.com with more than 30 years of experience covering mass tort litigation, environmental policy, and consumer safety. He previously served as Associate Editor at Inside the EPA and contributes original reporting on product liability lawsuits, regulatory failures, and nationwide litigation trends. Tags: Abilify, Antipsychotics, Childrens Drugs, Medication Error, Prescription Mistake, Risperdal Image Credit: |More Risperdal Lawsuit Stories Risperdal Side Effects Led to Deadly Breast Cancer, Lawsuit Claims January 7, 2026 Court Considers Remanding Risperdal Breast Cancer Lawsuit to California State Court October 29, 2025 Case Study Suggests Even Low-Dose Risperdal Side Effects May Cause Tardive Dyskinesia Movement Disorders December 14, 2022 0 Comments LinkedInThis field is for validation purposes and should be left unchanged.Share Your CommentsFirst Name*Last NameEmail* Shared Comments*This field is hidden when viewing the formI authorize the above comments be posted on this page Yes NoPost Comment I authorize the above comments be posted on this pageWeekly Digest Opt-In Yes, send me a weekly email with the latest lawsuits, recalls and warnings.Want your comments reviewed by a lawyer?To have an attorney review your comments and contact you about a potential case, provide your contact information below. This will not be published.Contact Phone #Alt Phone #Private CommentsNOTE: Providing information for review by an attorney does not form an attorney-client relationship.CAPTCHAGA SourceGA CampaignGA MediumGA ContentGA TermΔ MORE TOP STORIES Depo-Provera Meningioma Warning Update Should Be Added to Birth Control Shot: Lawsuit (Posted: today)A Depo-Provera meningioma lawsuit argues that Pfizer had a duty to warn women about scientific evidence linking the birth control shot to potential brain tumor growth yet failed to do so.MORE ABOUT: DEPO-PROVERA LAWSUITHearings on Evidence That Depo-Provera Causes Meningioma Brain Tumors Set for Late June 2026 (04/15/2026)High-Risk Brain Tumor From Depo-Provera Requires Frequent Monitoring, Lawsuit Claims (04/06/2026)Depo-Provera Meningioma Lawyers Reappointed to MDL Leadership Roles (03/25/2026) Judges Will Consider MDL for Dupixent Cancer Lawsuits Late Next Month (Posted: yesterday)A group of federal judges will determine whether all Dupixent cancer lawsuits should be formed into a multidistrict litigation, following oral arguments set for May 28.MORE ABOUT: DUPIXENT LAWSUITDupixent Injections Caused Peripheral T-Cell Lymphoma (PTCL) Diagnosis: Lawsuit (04/06/2026)Link Between Dupixent and CTCL Withheld From Users, Medical Community: Lawsuit (03/31/2026)Drug Makers Agree Dupixent Cancer Lawsuits Should Be Centralized in MDL (03/26/2026) SCS Injury Lawsuit Alleges Unlicensed Abbott Representatives Modified Device After Implantation (Posted: 2 days ago)A product liability lawsuit alleges unlicensed Abbott representatives made real-time spinal cord stimulator programming decisions based on a Texas womanโs responses, improperly modifying the device and contributing to her injuries.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITWaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (04/14/2026)Boston Scientific Neuromodulation Lawsuit Claims Spinal Cord Stimulator Exacerbated Chronic Pain (04/08/2026)Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (04/03/2026)
Case Study Suggests Even Low-Dose Risperdal Side Effects May Cause Tardive Dyskinesia Movement Disorders December 14, 2022
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