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Risperdal® (Risperidone) is an atypical antipsychotic drug which has been linked to serious and potentially permanent side effects such as:
Gynecomastia – boys developing breasts.
Tardive Dyskinesia – uncontrollable movement of face, tongue, and mouth.
Heart attack from heart attack (cardiac arrhythmias and other cardiac causes).
Diabetes.
We are investigating the link between Risperdal and gynecomastia(breast development in boys and adolescent males).
If you or a loved one has suffered from gynecomastia, please contact us today for a free, no-cost no-obligation evaluation of your situation.
About Harman Law LLC
Harman Law LLC is a national law firm that fights for justice for those who have been harmed – physically or financially – by someone who refuses to do what’s right. Contact us today by filling out a questionnaire, or by calling our toll free number (1-888-554-4672) for a no-cost no-obligation preliminary evaluation of your case.
Harman Law filed a complaint and is continuing to pursue defendants on behalf of a child who developed leukemia specific to benzene exposure while living near a petroleum transport station. For years, the station used by BP, Chevron, Gulf and other oil companies illegally disposed of toxic material including benzene resulting in documented contamination of the ground near the family’s home and in their drinking water supply.
The complaint is filed in the Superior Court of Athens-Clarke County, Georgia by Harman Law LLC and Nidel Law PLLC of Washington, D.C.
Related information
J.M. as Parent and next friend of minor son J.M.M. v. BP Products North America Inc.; Chevron U.S. A. Inc.,; Gulf Oil Corporation; Union Oil Company of California; Transmontaigne Product Services, Inc.: Transmontaigne Product Services Inc. East; Louis Dreyfus Highbridge Energy LLC; Colonial Pipeline Company; and Plantation Pipe Line Company
From the CNN Atlanta studios, Attorney Matthew Harman appeared on the legal television program The American Law Journal discussing the U.S. Food and Drug Administration.
Parents of premature babies in a four-year study of oxygen level treatment were not sufficiently warned of the potential dangers of the experiments. The families of over one thousand babies could have been at risk of blindness, brain damage or death as a consequence of their participation in the research.
The U.S. Department of Health and Human Services criticized lead researchers at the nearly two dozen participating medical schools for inadequate informed consent. Emory University Medical School in Atlanta participated in the study.
The attorneys at Harman Law Firm are investigating any harm to babies that may have occurred during their involvement in the research. If you or a family you know has an infant who was in the study at Emory or any research center who experienced a health problem contact our firm immediately to learn your options and protect the child’s health in the future. Fill out our contact form, email info@harmanlaw.com, or call toll-free 888-554-2762.
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The Harman Law Firm has filed a complaint against the manufacturer of the Medtronic MiniMed Paradigm MMT 722 Insulin Pump following the death of a young woman who was using the device.
The MiniMed Insulin Pump is designed to deliver insulin continuously into the body, making multiple injections per day unnecessary. The young college student with the MiniMed pump died from “diabetic ketoacidosis,” a condition that results from uncontrolled blood sugar that can quickly lead to heart failure, kidney failure, coma or death.
The complaint alleges that the MiniMed pump was defective and malfunctioned and that the manufacturer tested the pump following the woman’s death and concluded that the pump was in fact defective with a “faulty microchip” and “broken solder on joint on the interface board.” The manufacturer’s testing also concluded that the pump was “unable to prime,” meaning it could not eliminate air in the system so that it could pump the correct amount of pure insulin.”
Attorney Matthew Harman and the firm’s associates are continuing to investigate injuries that may be a result of using any of Medtronic drug pump model, including the recalled SynchroMed II and SynchroMed EL in addition to the MiniMed Paradigm insulin pump. For more information, see this page on the recall of Medtronic drug pumps.
If you or someone you know has experienced harm from a Medtronic drug or insulin pump, contact us for a free, no obligation consultation to learn your rights. You may be entitled to compensation, though there may be a time limit to file a claim.
If you are currently experiencing any health-related issues, consult your medical professional immediately.
If you have a knee or hip implant, please contact us to see if you are entitled to compensation. Several makes and models have either been recalled or have had manufacturers issue warnings. Harman Law Firm is investigating and available for free, no obligation consultations.
This website is designed for general information only. The information contained on this site does not constitute legal advice and does not form an attorney-client relationship.
