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What is Eskatrol used for? A Look Back at This Discontinued Medication

2 min read

In the early 1980s, Eskatrol was among the 200 most commonly-prescribed medications in the U.S., marketed as a "diet pill". For those asking what is eskatrol used for, this combination drug was an appetite suppressant before being withdrawn from the market by the U.S. Food and Drug Administration (FDA).

Quick Summary

Eskatrol was a prescription weight-loss drug containing dextroamphetamine and prochlorperazine, used as an appetite suppressant until its withdrawal by the FDA in 1981 due to concerns over abuse and lack of demonstrated long-term efficacy.

Key Points

  • Historical Appetite Suppressant: Eskatrol was formerly used as a prescription diet pill for weight loss.

  • Dual-Ingredient Formula: It contained dextroamphetamine sulfate and prochlorperazine.

  • Mitigated Side Effects: Prochlorperazine was included to potentially manage emotional stress and counteract some stimulant side effects.

  • FDA Withdrawal: The FDA mandated its withdrawal in 1981 due to the manufacturer failing to prove its long-term therapeutic effectiveness.

  • Discontinued and Obsolete: Eskatrol is no longer legally available.

  • Amphetamine-Related Risks: The high potential for abuse and dependence contributed to regulatory scrutiny and removal.

In This Article

The Dual-Action Formulation of Eskatrol

Eskatrol contained dextroamphetamine sulfate, a central nervous system (CNS) stimulant and appetite suppressant, and prochlorperazine, a typical antipsychotic. Dextroamphetamine is also known as Dexedrine when marketed alone. Prochlorperazine, known under the brand name Compazine, was included possibly to manage emotional stress during dieting and potentially lessen some stimulant side effects like excitability. The combination aimed for a balanced approach to weight loss.

The Rise and Regulatory Scrutiny of Amphetamine-Based Diet Pills

Amphetamines were widely prescribed for weight loss in the 1960s and 70s. However, concerns grew regarding their long-term effectiveness and potential for abuse. In August 1970, the FDA restricted amphetamines for obesity to short-term use and increased hazard warnings.

FDA Mandates Eskatrol Withdrawal in 1981

In 1981, the FDA ordered Eskatrol's manufacturer, Smith, Kline & French, to stop production and remove the drug from the market. The FDA stated that the company failed to provide sufficient evidence of Eskatrol's long-term therapeutic efficacy. Concerns about amphetamine abuse were also a factor.

Comparison: Eskatrol vs. Modern Weight-Loss Medications

Weight-loss medication has evolved significantly since Eskatrol's discontinuation. Modern treatments prioritize safety, long-term effectiveness, and lower abuse risk. Here is a comparison:

Feature Eskatrol (Discontinued) Phentermine (e.g., Adipex) GLP-1 Agonists (e.g., Wegovy)
Active Ingredients Dextroamphetamine, Prochlorperazine Phentermine Semaglutide
Primary Mechanism Appetite suppression (amphetamine) & emotional management (prochlorperazine) Short-term appetite suppression via CNS stimulation Mimics GLP-1 hormone, regulating appetite and food intake
Market Status Withdrawn in 1981, unavailable Currently available by prescription for short-term use Newer, available by prescription for long-term use
Abuse Potential High due to amphetamine content Present, but less than dextroamphetamine; a controlled substance No known abuse potential
Duration of Use Initially marketed for longer, but restricted to short-term Short-term (generally 12 weeks) Indicated for long-term weight management
Effectiveness Failed to prove long-term efficacy Proven effective for short-term loss Demonstrated significant and sustained weight loss

The Legacy of Eskatrol and Amphetamines in Pharmacology

Eskatrol's history highlights how pharmacological regulations and the understanding of addiction have advanced. Its high potential for psychological dependence and side effects were major factors in the FDA's decision. The inclusion of an antipsychotic to counterbalance a stimulant proved insufficient.

Eskatrol's story underscores the importance of:

  • Demonstrated Efficacy: The need for strong, long-term studies to prove a drug's effectiveness, which Eskatrol lacked.
  • Considering Abuse Potential: Recognizing the risks of prescribing controlled substances, particularly for chronic conditions.
  • Prioritizing Safety: Modern drug development focuses heavily on minimizing side effects and abuse potential.

Conclusion

In summary, what is Eskatrol used for was as an appetite suppressant for weight loss, but it is a medication firmly in the past. Its dual-action formulation combined a stimulant with an antipsychotic in a now-obsolete approach. Driven by safety concerns, high dependence risk, and lack of proven long-term efficacy, the FDA removed Eskatrol from the market in 1981. Today, safer and more effective alternatives exist for medical weight management.

Frequently Asked Questions

No, Eskatrol was withdrawn by the FDA in 1981 and is no longer available. Prescribing it is illegal.

Eskatrol contained dextroamphetamine sulfate and prochlorperazine.

The FDA ordered its discontinuation in 1981 because the manufacturer could not provide adequate evidence of its long-term effectiveness. Concerns over the abuse potential of its amphetamine component also played a significant role.

While Eskatrol is discontinued, dextroamphetamine is still prescribed today for conditions such as ADHD and narcolepsy.

Safety concerns, particularly the high potential for abuse and dependence due to the amphetamine component, were a key factor in the FDA's decision to withdraw it.

The amphetamine component could cause nervousness, insomnia, and psychological dependence. Antipsychotics like prochlorperazine also carry risks of side effects.

No single medication replaced Eskatrol. Modern weight-loss options include a range of prescription drugs, such as phentermine and GLP-1 agonists (e.g., Wegovy), which are subject to stricter regulatory standards.

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Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice.