Zyrtec, an antihistamine used to treat allergies, was taken off the market in the United States in 2007. The reason for this was due to an increase in the number of reports of serious side effects associated with the drug, including liver damage and increased risk of stroke.
History of Zyrtec
Zyrtec was first introduced in the United States in 1996. It was developed as an alternative to other antihistamines such as Claritin and Allegra. It was initially marketed as a non-sedating antihistamine, meaning it would not cause drowsiness.
Side Effects Linked to Zyrtec
In 2006, the U.S. Food and Drug Administration (FDA) began receiving reports of serious side effects associated with the use of Zyrtec. The most common side effects reported included liver damage, increased risk of stroke, and seizures.
Decision to Take Zyrtec Off the Market
In 2007, after a review of the available data, the FDA concluded that the risks associated with Zyrtec outweighed its benefits and decided to take it off the market. The FDA also issued a warning to healthcare providers to stop prescribing the drug and to patients to stop taking it.
Alternatives to Zyrtec
After Zyrtec was taken off the market, patients were advised to switch to other antihistamines such as Claritin or Allegra. These drugs are considered to be safer and do not carry the same risks as Zyrtec.
