NDAORALTABLET
Approved
Jul 2003
Lifecycle
LOE Approaching
Competitive Pressure
30/100
Data completeness
2/8 — Basic
Drug data last refreshed 1h ago · AI intelligence enriched 1w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
PEXEVA (paroxetine mesylate) is an oral selective serotonin reuptake inhibitor (SSRI) approved in 2003 for the treatment of depression, anxiety disorders, and related conditions. It works by increasing serotonin availability in the central nervous system to alleviate mood and anxiety symptoms. The mesylate salt formulation was developed to improve bioavailability and patient tolerability compared to earlier paroxetine formulations.
$0.508MPart D
LOE ApproachingDeclining
This product is in decline with minimal commercial infrastructure, indicating reduced hiring and focus on managed care or specialty roles rather than growth-oriented positions.
Mechanism of Action
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Career Relevance
Working on PEXEVA offers limited career advancement potential due to the product's LOE-approaching lifecycle and minimal market presence (0 linked jobs). Roles tend to focus on defending market share, managing payer relationships, and optimizing formulary placement rather than launch excitement or growth initiatives.
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Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.