Posts Tagged ‘Complications’

Mercury Dental Fillings: Self Induced Recall Required

Wednesday, July 15th, 2009

 Amalgam dental fillings containing 50% mercury were the only option for people with cavities in former years. Over the past ten years, dentists have been inclined to select resin dental filling materials following the culmination of reports showing adverse reactions to mercury in the mouth.

  •  In 2002, the FDA recalled mercury containing ointment and all mercury containing products used in animals because of its toxicity.
  •   The Environmental Protection Agency indicted that 1 of 7 American women of childbearing age has enough mercury in their mouths to be at risk for bearing a brain-damaged child. 
  •   In June 2009, The Wealthy Dentist published the results of a poll showing that over 50% of all 116,000 dentists have abandoned the use of mercury containing dental fillings. Yet, there has not been an FDA Recall of mercury fillings to date.    

 

Self Induced Recall Required

It is clear that the toxicity caused by mercury containing products is a health risk. People with mercury fillings should speak with their dentist about replacing amalgam fillings with those of resin material. Dental insurance providers do cover composite resin materials. Though, benefits may among insurance companies and reimbursement may be limited to the cost of an amalgam dental filling.

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Ethex Recall: Over-Dose Tablets Pose Risks

Thursday, May 21st, 2009

By Lesley Ranft

Ethex Corporation announced multiple recalls of numerous drugs, including morphine, iron and prenatal vitamins. The string of recalls began to commence last year due to double dose tablets of morphine and other potential concerns. There have been recent reports that the FDA is questioning adequate quality control at the manufacturing facility where the morphine tablets were made. As Richard Schulte, Attorney at Law of Dayton, Ohio explains, “This is a clear case of manufacturer defect. The problem we are faced with now is we do not yet know the extent of defective pills on the market and how great of harm they caused to consumers.”

Signs of Overdose
The long term effects of the prenatal vitamins are unknown. Iron supplement overdose side effects usually occur shortly after intake. Iron poisoning side effects may include, vomiting diarrhea, liver dysfunction, jaundice, internal bleeding, and seizures.-1- The initial signs of overdose in morphine are clear and can be life threatening, but may not be fully apparent to the person using the drug. Opioid overdose includes:
• Rapid Heart Beat
• Hypertension
• Tremors
• Bluish Lips
• Headache
• Insomnia
• Dizziness and Fainting
• Blurred vision
• Upset stomach
• Fainting
• Low Blood Pressure

The List of Ethex Recalls

Isosorbide mononitrate: 30mg and 60mg
Propafenone HCI: 150mg, 225mg, and 300 mg
Dextroamphetamine sulfate tablets: 5mg and 10mg
Morphine sulfate ER: 15mg, 30mg, 60mg, 100mg 200mg
Morphine IR: 15mg and 30mg

Prenatal Vitamin Recalls
Advanced NatalCare® Tablets and Advanced-RF NatalCare® Tablets
Cal-Nate™ Tablets
CareNatal™ DHA Tablets
ComBgen Tablets
ComBiRx™Tablets
NataCaps Capsules
NatalCare Gloss, PIC, PIC Forte, Plus, Rx, Three Tablets
NataTab FA Tablets
NataTab RX Tablets
NutriNate® Chewable Tablets
NutriSpire™ Tablets
Prenatal MR 90 FE and MTR w/Selinium Tablets
Prenatal Rx 1 Tablets
Prenatal Z, Advanced Formula Tablets
Ultra NatalCare Tablets

Iron Supplement Recalls
Anemagen Caplets
Anemagen Forte Caplets
Conison™ Capsules
Fe-Tinic™ 150 Forte Capsules

-1- http://www.merck.com/mmhe/sec24/ch297/ch297h.html

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Depakote Warning: Children Have Lower IQ’s

Wednesday, May 13th, 2009

Study results published in the New England Journal of Medicine have demonstrated that depakote, aka Valproate, used during pregnancy may result in the child having a lower IQ. Depakote has also been associated with a high rate of fetal death and birth defects such as spina bifida in children of mothers who used Depakote. The study was performed by Dr. Kimford Meador of Emory University and a team of researchers.

Depakote is used to treat epileptic seizures, mood disorders and migraine headaches. The study followed pregnant women in the U.S. and England that had taken anti-seizure medications between 1999 and 2004.The study compared the IQ scores of children by 3 years of age whose mothers had taken one of four types of anti-seizure medications, including: depakote, lamotrigine (also known as lemectal), phenytoin, and carbamazepine. The study results showed that Depakote children ranked six to nine points lower on the IQ scale when compared to children whose mothers took other anti-seizure medications. The average IQ for a “Depokote child” was 92. The IQ ranges of the other children were between 98 and 101. The average rating for a child’s intelligence is 100. The study results also demonstrated that the higher the dosage that the “Depakote mother” received, the lower the IQ the child had. Dosage levels were irrelevant in the other anti-seizure medications.

In 2007, Meader study results presented at the American Academy of Neurology showed a marked risk for retardation in children whose mothers had taken Depakote. This rate of risk was twice as great as the risk associated with other anti-seizure medications. Twenty four percent of the children who mother took depakote and participated in Meador’s study had an IQ level that is associated with retardation.

According to the Alliance for Human Resource Protection, approximately 25,000 U.S. children are born to women who have epilepsy annually. It is important to note that just because the other anti-seizure medications are not associated with an elevated risk for lower IQ’ed children, does not mean that there are not other types of risks for injury. For example, there have been reports that lemectal is associated with Steven’s Johnson Syndrome, a life threatening and severely debilitating condition.

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Denture Cream Dangers Uncovered through Lawsuits

Saturday, May 9th, 2009

Dentures Creams such as Polydent and Fixodent have shaken up the medical community as much as the legal community over the past year. In mid 2008, the results of a study were published in Neurology, a journal for Neurologists, showing a link between denture cream use and neurological health issues. The University of Texas Southwestern Medical Center study authors suggested that excessive zinc exposure was at the core of the problems. The published findings carried a warning: one denture cream tube should last up to 10 weeks, but study participants were using two tubes each week.

Dental Cream Health Problems
By 2009, dental creams health issues were reported by numerous people from across the U.S. to lawyers. High levels of zinc may deplete copper in the body. The simultaneous effects of excess zinc and diminished copper may lead to serious and permanent health issues, including.

• Premature Tooth Loss
• Numbness
• Pain
• Weakness in the arms, legs, hands and feet
• Body sores
• Water retention
• Hair loss
• Anorexia
• Fatigue
• Anemia
• Difficulty breathing
• Paralysis
• Immune disorders
• Cardiovascular disorders
• Bone marrow disorders

Proof is in the Study
The University of Texas Southwestern Medical Center research team found that participants had comprising levels of zinc and copper in their bodies. Study participants were also suffering from health problems.
• Zinc blood levels were over the normal range by .36-3.18
• Copper levels were between 0.1 and .23, normal copper levels range from 0.75 to 1.45

This imbalance is suspected to be the cause of the described symptoms above. In fact, there may be other symptoms that have not been uncovered at this time. Personal injury attorneys are often some of the first people to know about problems such as those caused by denture creams. If you feel you have been injured by your use of dental cream, select personal injury attorneys are available to speak with you.

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Kugel Mesh Patch Lawsuits

Friday, May 8th, 2009

By Lesley Ranft

The Kugel Mesh Patch was meant to provide a solution for people suffering from hernias. There are 700,000 hernia surgeries performed each year. Yet, no one knew of the problems associated with the Kugel Mesh patch which is meant to be permanently inserted into the treatment area of the body. Unfortunately, there are many potential victims that have been exposed to faulty Kugel Mesh Patches. As early as 2001, reports of complications accumulated, but the Kugel Mesh maker did not conduct a product recall until 2007. As Joe Saunders, Attorney at Law, of Pinnellas Park, Florida explains, “It appears that there has been a failure to design out and guard against the risk of injury from the Kugel Mesh. The abdominal Kugel Mesh is subject to breakage which can puncture an organ. The mesh itself is prone to lose rigidity and may roll up inside the body which creates the risk of the tissue adhesions and other complications.” Complications resulting from the use of the Kugel Mesh Patch include:

• Bowel Obstruction
• Bowel Adhesions
• Constipation
• Abdominal pain
• Fever
• Bowel Perforation
• Tissue Adhesions
• Liver damage
• Liver failure

Several lots of the Kugel Mesh Patch for hernia repair had been recalled in the beginning of 2008. The final recall involving numerous lots of the drug did not come until after an initial 2007 recall of a select type of the Kugel Mesh Patch. Davol, the Kugel Patch manufacturer, had received an unusual number of complication reports from Kugel Mesh Patch users. Soon, the company uncovered defects in the memory recoil ring, including breakage of the ring, which may produce serious complications for patients using the ring. The lots with possible problems are those from December of 2005, March of 2006 and January of 2007. As Ed Jazlowiecki, Attorney at Law of Bristol, Connecticut explains, “The Kugel Mesh Patch has caused a significant number of serious injuries, including bowl perforation which requires surgery and is associated with risks for complications and death. This is particularly disturbing when there are better products on the market.”

Kugel Mesh Patch Recovery
Patients that received a Kugel Mesh Patch from one of the defective lots may be subject to surgery for the removal of the Kugel Mesh Patch. In addition, people receiving the Kugel Mesh may be subject to long term complications that inhibit daily life. As Kate Gillespie, Attorney at Law of Baum, Hedlund, Aristei & Goldman, P.C.explains, “People whose doctors do not know about the Kugel Mesh defects often tell patients to be patient and wait it out. So, people think their problems will resolve themselves shortly. They soon learn that their problems are just the beginning and recovery may be a life long commitment.”

Reports of long term medical issues from the Kugel Mesh Patch include: muscle and tissue adhesions whereby the sticky surface of the mesh adheres to the intestines, stomach or surrounding tissue. Bowel infection, perforation and seaping wounds have also been documented. As Kate Gillespie explains, “The hernia operation is a simple procedure that does not usually involve unmanageable complications. Unlike the Kugel Mesh Patch, a hernia operation often involving permanent uncomfortable injuries.”

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