If you are a victim of acute or chronic oral thrush, Levothyroxine may be able to help you. As a matter of fact, the drug has been approved by the Food and Drug Administration (FDA) for treating the condition. However, there have been cases in which individuals have been identified as having oral thrush when they received Levothyroxine. The question that arises is whether these individuals’ underlying problems with oral thrush were caused by the drug or if they developed the condition after they received the medication.
- 1 In many cases, it is difficult to pinpoint whether a person was exposed to certain conditions or elements which made the condition worse.
- 1.1 Because some individuals are particularly sensitive to specific ingredients, they may be more apt to develop a reaction.
In many cases, it is difficult to pinpoint whether a person was exposed to certain conditions or elements which made the condition worse.
For instance, if an individual has a family history of allergies or cancer, it is not uncommon for that individual to be reactive to certain elements. It is often difficult to determine whether a reaction occurred prior to taking Levothyroxine or after using the medication. This is especially true in infants, children, or the elderly.
Because some individuals are particularly sensitive to specific ingredients, they may be more apt to develop a reaction.
For example, some individuals experience an allergic reaction to a component known as l-lysine. Others experience reactions to an amino acid called l-histidine. Still others may only have reactions to one of the many different ingredients contained in Levothyroxine.
The manufacturer of Levothyroxine has faced many legal issues over the years.
In recent years, a class action suit was brought against GlaxoSmithKline, the manufacturer of the drug. Class action lawsuits allow multiple plaintiffs to pool their resources and pay legal fees associated with a legal case. Plaintiffs in these types of cases typically receive a percentage of the total settlements of all the individual plaintiffs. If a GlaxoSmithKline representative is named as a defendant, it is possible that the drug manufacturer could be ordered to pay out millions of dollars.
The Food and Drug Administration approved Levothyroxine for sale as an oral contraceptive in July 2021.
The manufacturer knew the drug could have dangerous side effects, but offered the product anyway. It was also known at the time that the drug had not been tested safely on women who already had hormone-related problems such as polycystic ovarian syndrome. It is currently being studied by the Center for Disease Control to see if it has any affect on heart disease or blood clots.
Currently, the plaintiffs in this lawsuit have been granted class action status. This means that they are able to bring the case together as a class. They will be able to receive compensation without having to prove that they actually have been affected by the deficiency. To determine who will receive compensation, however, the court will need to determine what percentage of plaintiffs in a certain group suffer from the deficiency. The court is not expected to rule definitively on the issue until at least a year after the case is settled. This delay allows the parties to negotiate compensation and develop a schedule for how much the settlement will pay out.
Levothyroxine is the most prescribed oral contraceptive in the United States.
Approximately 12 million American women take the drug on a yearly basis. Many women take the drug because they have severe allergies or they have a medical condition that makes it unsafe for them to take other oral contraceptives. Some women also take the drug to control menopause symptoms. Women who are not allergic to the drug can use it to prevent pregnancy.
There have been other cases in which the FDA has received compensation when a manufacturer’s design was found to be defective. A member of the FDA, Dr. Arthur Sackler, went public with his findings in a report to the FDA. He argued that oral contraceptives made women more susceptible to breast cancer. His research showed that women who took the pill were more likely to develop ductal carcinoma in their breast. He called for a recall of the drugs and for all manufacturers to reformulate their products so that they do not put women at risk of developing this disease.