Celexa, which is the brand name for the medication citalopram, has not been taken off the market. It is still available and widely prescribed as a treatment for depression and anxiety disorders. However, there have been some concerns about the safety of Celexa in certain populations.
FDA Warning and Safety Concerns
In 2011, the U.S. Food and Drug Administration (FDA) issued a warning about the use of Celexa in individuals with certain genetic variations that affect the metabolism of the medication. Specifically, the warning stated that doses of Celexa greater than 40 mg per day should not be used in individuals with the genetic variation known as CYP2C19 poor metabolizers, as this can lead to an increased risk of heart problems.
The FDA also warned that the use of Celexa and other similar medications, known as selective serotonin reuptake inhibitors (SSRIs), can increase the risk of suicidal thoughts and behavior in children, adolescents, and young adults. It is important to closely monitor individuals taking Celexa for signs of suicidal thoughts or behavior, particularly when starting the medication or adjusting the dosage.
Effectiveness and Safety
Overall, Celexa is considered to be an effective and safe medication for treating depression and anxiety disorders when used as prescribed by a healthcare provider. Like all medications, it can cause side effects in some individuals, and it is important to discuss any potential risks and benefits with a healthcare provider.
In conclusion, Celexa has not been taken off the market. While there have been some concerns about the safety of the medication in certain populations, it is still widely prescribed and considered to be an effective and safe treatment for depression and anxiety disorders when used as prescribed by a healthcare provider. It is important to closely monitor individuals taking Celexa for any signs of side effects or suicidal thoughts or behavior.