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Published by Defective Product | Drug Recall Lawyers Based in Missouri, Carey, Danis & Lowe

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  • Dialysis Machine Recalled for Potential for Death or Serious Injury
  • Senate Investigation of Avandia Shows Manufacturer Knew About Risks Years Ago
  • FDA Puts Severe Restrictions on Use of Anemia Drugs in Cancer Patients
  • Study Shows Common Antidepressant Lowers Effectiveness of Breast Cancer Drug
  • FDA Issues Stronger Warning About Metabolic Problems for Teens Taking Zyprexa
  • Study Shows Anti Obesity Drug Raises Risk of Heart Attack or Stroke in Heart Patients
  • FDA Expands McNeil OTC Drug Recall, Rebukes Manufacturer for Yearlong Delay
  • Reports Find Nursing Homes Use Antipsychotics Off-Label Despite Safety Warnings
  • Analysis Finds Antidepressants Have Little or No Benefit for Mild Depression
  • FDA Requests Further Studies of Diabetes Drug Due to Reports of Pancreatitis
  • New Studies Show CT Scans Cause Tens of Thousands of Cancers Each Year
  • FDA Updates Antidepressant Warning Label to Include Risk of Sudden Cardiac Death
  • FDA Finds Greater Risk of Fatal Disorder From Certain MRI Drugs With Gadolinium
  • Jury in Prempro Trial Awards Illinois Woman $6.3 Million for Link to Breast Cancer
  • FDA Calls for New Labeling for Anesthetics Used in Post-Surgery Pain Pumps
  • Study Confirms Serious Blood Clot Threat From Anemia Drugs for Cancer Patients
  • Gadolinium Lawsuit Against GE Filed in St. Louis Circuit Court
  • Diabetes Drug Prescribing Information Revised to Reflect Reports of Kidney Problems
  • European Regulators Review Arthritis Drug Safety as FDA Announces New Case of Brain Infection
  • Suspected Defects in Power Cords for Medical Devices Spark FDA Investigation
  • FDA System for Tracking and Announcing Medical Device Recalls Faulted as Recalls Soar
  • FDA Warns Doctors and Parents About Dosage Discrepancy for Liquid Form of Tamiflu
  • FDA Orders Black Box Warning for Injected Sedative at Center of Supreme Court Case
  • Memo Introduced at Paxil Trial Suggests Drug Company May Have Buried Negative Studies
  • Drug Maker Pfizer to Pay Largest Criminal Fine Ever to Settle Allegations of Off Label Marketing
  • Scientists Question Findings in Study of Asthma Drugs Funded by Drug Manufacturer
  • FDA Announces Investigation Into Reports That Weight-Loss Drug Caused Liver Failure
  • Manufacturer Recalls Generic Adderall Because of Oversized Pills Posing Risk of Heart Problems
  • FDA Reviewing Data Suggesting Asthma Medication May Cause Heart Problems and Strokes
  • Black Box Safety Warning Ordered for Certain Children’s Drugs That Raise Risk of Cancer
  • FDA Requires Black Box Warning for Label of Gastrointestinal Drug Reglan
  • Merck and Schering-Plough Pay $5.4 Million to Settle Drug Cover-Up Suits
  • FDA Adds Black Box Warning to Painkillers Darvon and Darvocet Because of Risk of Fatal Overdose
  • Anti-Smoking Drugs Chantix and Zyban Get Black Box Warning About Risk of Suicide and Mental Illness
  • FDA Calls for Reduced Maximum Dosage of Common Pain Reliever Acetaminophen
  • FDA Seizes Most of Generic Company Caraco's Drugs Due to Manufacturing Mistakes
  • FDA Links Zicam to Permanent Sense of Smell Loss -- Other Homeopathic Products Under Scrutiny
  • FDA Recommends Suicidal Behavior Precaution for Singulair and Other Asthma Meds
  • New FDA Report Associates Liver Failure with Anti-Thyroid Drug
  • Analysis Shows Risk of Perforated Stomach or Bowels Rises Sharply With Use of Cancer Drug
  • Watchdog Group Asks FDA to Add Warning on Label of Constipation Drug That May Cause Miscarriage
  • Heparin-Linked Deaths Spur Fears About Repeat of 2008 Contaminated Prescription Drug Recall
  • FDA Announces Safety Recall of Diet Aid Hydroxycut Following Cases of Liver Damage and Death
  • Over-the-Counter Painkillers Must Carry Stronger Warnings of Potential Organ Damage, FDA Decides
  • FDA Gets Court Order Barring Pharmaceutical Company From Selling Unapproved and Unsafe Drugs
  • Congress Considering Restoring Patients’ Ability to File Defective Medical Device Lawsuits
  • Psoriasis Medication Removed from U.S. Market After Link to Brain Infection
  • Documents Show FDA Repeatedly Overruled Scientists’ Rejections in Menaflex Knee Device Approval
  • Congress Considers Legislation to Reverse Supreme Court Decision on Defective Medical Device Lawsuits
  • Unsealed Documents Show Pharmaceutical Company Buried Unfavorable Studies on Seroquel
  • U.S. Supreme Court Rules FDA Approval Does Not Bar Pharmaceutical Injury Lawsuits
  • FDA to Study Effects of TV Ads for Prescription Drugs on Consumers -- Missouri Pharmaceutical Liability Law Firm
  • FDA Panel Recommends Davron and Darvocet Be Removed From Market -- St. Louis Defective Prescription Drug Lawyer
  • FDA Recalls Dietary Supplement Containing Undeclared Controlled Substance -- St. Louis Dangerous Drug Attorney
  • Troubled Missouri Drug Manufacturer Pulls Almost All Products From Market -- Southern Illinois Drug Injury Law Firm
  • Prescription Painkiller Recalled Due to Potential for Dangerous Overdose -- St. Louis Dangerous Medication Law Firm
  • Defibrillator Lawsuits Against Medtronic Dismissed--Missouri Medical Device Attorney
  • Missouri to Receive $18 Million in Zyprexa Lawsuit -- St. Louis Defective Drugs Attorney
  • Johnson & Johnson Recalls Duragesic Patch Painkillers Due to Overdose Potential -- Illinois Defective Prescription Drug Lawyer
  • Heparin from China found to be contaminated with man-made chemical--defective drug attorney.
  • FDA Warns Public to avoid 69 Brands of Dangerous Diet Pills -- Missouri Defective Medication Attorney
  • Fluoroquinolone Antibiotics Such as Levequinn and Cipro Carry an Increased Risk of Tendon Rupture--Defective Drug Lawyer
  • Two Bowel-Cleansing Drugs Linked to Severe Kidney Injury -- Illinois Dangerous Drugs Attorney
  • Avastin Linked to Blood Clots and Cancer Drug According to a Recent Medical Study-- Missouri Defective Drug Law Firm
  • Drug Maker Wyeth Under Fire for Use of Ghostwriters -- St. Louis Defective Drug Lawyers
  • Cardiologist Warns of Lax FDA Regulations for New Implanted Defibrillator -- St. Louis Defective Medical Device Lawyer
  • Advisory Panel Recommends Ban of Two Asthma Drugs- Serevent and Foradil--Defective Drug Lawyer
  • Trasylol Dangers Confirmed in Latest Study
  • Duragesic Pain Patch Case-Jury Awards Nearly $16.6M in Damages
  • Mechanical Heart Pump Recalled
  • Artificial Blood Raises Risk of Death, Heart Attack
  • Trasylol Supplies Finally Pulled by Bayer
  • Canadian Trasylol Study Results Announced
  • Top FDA Staff Opposed the Bush Administration's Attempt To Shield Drug Companies
  • Fen-Phen Trial Results in $3 Million Jury Verdict
  • Pfizer Agrees to Settle Celebrex and Bextra Claims for $894 Million
  • Transvaginal Surgical Mesh is the Subject of a FDA Public Health Notification
  • Deaths Linked to Anti-Anemia Drugs Probed
  • Supreme Court to Decide Appeal Filed by Wyeth against Amputee
  • Medtronic Infusion Pump Recalled by the FDA
  • Trasylol Pulled From the Market and Can Only be Used for Investigational Use
  • Trasylol Pulled From the Market and Can Only be Used for Investigational Use
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Topics

  • Dangerous Drugs
  • Dangerous Medical Devices
  • Drug Safety
  • Jury Verdicts

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Recent Entries

  • March 4, 2010 1:17 PM
    Dialysis Machine Recalled for Potential for Death or Serious Injury Over the past two years, Baxter International Inc. has received...
  • February 23, 2010 3:08 PM
    Senate Investigation of Avandia Shows Manufacturer Knew About Risks Years Ago As a dangerous prescription drug attorney,I have paid close attention...
  • February 19, 2010 8:37 AM
    FDA Puts Severe Restrictions on Use of Anemia Drugs in Cancer Patients I wrote here last week about a heightened risk of...
  • February 10, 2010 9:44 AM
    Study Shows Common Antidepressant Lowers Effectiveness of Breast Cancer Drug As a dangerous drug attorney, I was interested to see...
  • February 2, 2010 4:02 PM
    FDA Issues Stronger Warning About Metabolic Problems for Teens Taking Zyprexa The psychiatric drug Zyprexa (olanzapine) has been at the center...

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Phone: (877) 678-3400 Fax: (314) 678-3401 jeff@jefflowepc.com

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