You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 22, 2024

Q-GESIC Drug Patent Profile


✉ Email this page to a colleague

« Back to Dashboard


When do Q-gesic patents expire, and when can generic versions of Q-gesic launch?

Q-gesic is a drug marketed by Quantum Pharmics and is included in one NDA.

The generic ingredient in Q-GESIC is aspirin; meprobamate. There are twenty-two drug master file entries for this compound. Additional details are available on the aspirin; meprobamate profile page.

AI Research Assistant
Questions you can ask:
  • What is the 5 year forecast for Q-GESIC?
  • What are the global sales for Q-GESIC?
  • What is Average Wholesale Price for Q-GESIC?
Summary for Q-GESIC
US Patents:0
Applicants:1
NDAs:1
Raw Ingredient (Bulk) Api Vendors: 36
DailyMed Link:Q-GESIC at DailyMed
Drug patent expirations by year for Q-GESIC

US Patents and Regulatory Information for Q-GESIC

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Quantum Pharmics Q-GESIC aspirin; meprobamate TABLET;ORAL 088740-001 Jun 1, 1984 DISCN No No ⤷  Subscribe ⤷  Subscribe ⤷  Subscribe
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

Q-GESIC Market Analysis and Financial Projection Experimental

Market Dynamics and Financial Trajectory for Dextropropoxyphene (Q-GESIC)

Introduction

Dextropropoxyphene, marketed under various names such as Darvon, Darvocet, and Q-GESIC, is a prescription opioid analgesic that has been subject to significant market and regulatory changes over the years. This article will delve into the market dynamics and financial trajectory of dextropropoxyphene, highlighting its availability, regulatory status, and the impact of these factors on its market presence.

Historical Context and Regulatory Status

Dextropropoxyphene was widely used in the past for managing mild to moderate pain. However, due to concerns over fatal overdoses and heart arrhythmias, it has been withdrawn from the market in several countries, including Europe and the United States[1].

United States

In the U.S., dextropropoxyphene was available in combination with acetaminophen under the brand name Darvocet. However, the FDA directed its recall due to safety concerns, effectively removing it from the U.S. market[1].

Europe

In the UK, dextropropoxyphene was part of the co-proxamol formulation, which also contained a subtherapeutic dose of paracetamol. Despite warnings, the drug was associated with a high risk of overdose, leading to its phased withdrawal from the market. This decision was controversial, with some patients finding alternative analgesics too strong, too weak, or with intolerable side effects[1].

Australia

In Australia, dextropropoxyphene is still available on prescription, both in pure form and in combination with paracetamol. However, its use has been restricted, and it was initially set to be withdrawn from the market in 2012. Following a review, the drug was allowed to be sold under strict conditions[1].

Market Impact of Regulatory Changes

The regulatory changes have significantly impacted the market dynamics of dextropropoxyphene.

Reduced Prescriptions

The withdrawal of dextropropoxyphene from several major markets has led to a substantial reduction in prescriptions. For example, in the UK, the number of patients prescribed co-proxamol dropped from 1.7 million to 70,000 following its phased withdrawal[1].

Alternative Treatments

The removal of dextropropoxyphene has forced patients and healthcare providers to seek alternative pain management options. This shift has benefited other pharmaceutical companies that offer safer and more effective analgesics.

Financial Consequences

The financial trajectory of dextropropoxyphene has been severely impacted by its regulatory status. Companies that once relied on the sales of this drug have had to diversify their product portfolios to maintain revenue.

Financial Trajectory

Revenue Decline

The recall and withdrawal of dextropropoxyphene have resulted in a significant decline in revenue for companies that manufactured and distributed the drug. This decline has forced these companies to focus on other products and expand their portfolios to compensate for the loss.

Diversification Strategies

Companies have adopted various strategies to mitigate the financial impact. For instance, they have invested in research and development to introduce new products, acquired other pharmaceutical companies, and entered into co-development or co-promotion partnerships to strengthen their market position[3].

Market Dynamics Post-Withdrawal

Shift to Safer Alternatives

The market has shifted towards safer and more effective pain management options. This shift has been driven by regulatory actions and the need for healthcare providers to prescribe medications with better safety profiles.

Competitive Landscape

The competitive landscape in the pain management market has become more dynamic, with several new entrants and existing players expanding their offerings. This competition has driven innovation and improved patient outcomes.

Patient Impact

Access to Alternatives

Patients who were previously prescribed dextropropoxyphene have had to adapt to new treatments. While some have found suitable alternatives, others have faced challenges in finding medications that effectively manage their pain without the associated risks of dextropropoxyphene[1].

Patient Safety

The regulatory actions have ultimately enhanced patient safety by removing a drug with significant risks from the market. This has reduced the incidence of fatal overdoses and heart arrhythmias associated with dextropropoxyphene.

Conclusion

The market dynamics and financial trajectory of dextropropoxyphene have been significantly influenced by regulatory actions and safety concerns. The drug's withdrawal from major markets has led to a decline in prescriptions and revenue, forcing companies to diversify and invest in safer and more effective pain management options.

Key Takeaways

  • Regulatory Impact: The withdrawal of dextropropoxyphene from several markets due to safety concerns has drastically reduced its market presence.
  • Financial Consequences: Companies have experienced a decline in revenue and have had to diversify their product portfolios.
  • Market Shift: The market has shifted towards safer and more effective pain management options.
  • Patient Safety: Regulatory actions have enhanced patient safety by reducing the risk of fatal overdoses and heart arrhythmias.

FAQs

What is dextropropoxyphene, and why was it withdrawn from the market?

Dextropropoxyphene is an opioid analgesic that was withdrawn from several markets due to concerns over fatal overdoses and heart arrhythmias.

Is dextropropoxyphene still available in any countries?

Yes, it is still available on prescription in Australia, albeit under strict conditions.

How has the withdrawal of dextropropoxyphene affected patient care?

Patients have had to adapt to new pain management treatments, with some facing challenges in finding suitable alternatives.

What strategies have companies adopted to mitigate the financial impact of dextropropoxyphene's withdrawal?

Companies have diversified their product portfolios, invested in research and development, and entered into co-development or co-promotion partnerships.

How has the competitive landscape in the pain management market changed?

The market has become more dynamic with a focus on safer and more effective pain management options, driving innovation and improved patient outcomes.

Sources

  1. Wikipedia: Dextropropoxyphene
  2. Clinical and Experimental Emergency Medicine: CEEM Journal
  3. Supernus Pharmaceuticals: 2021 Annual Report
  4. United Nations Office on Drugs and Crime: World Drug Report 2017
  5. American Journal of Neuroradiology: Complete Issue (PDF)

More… ↓

⤷  Subscribe

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.