PPX
Propxyphene
Primary Products
DrugSURE® Integrated Test Cups
DrugSURE® Dip Tests
OralTox® Oral Fluid Tests
What is PPX?
Propoxyphene (PPX) is a synthetic opioid analgesic that was once commonly prescribed for mild to moderate pain. Structurally similar to methadone but significantly weaker, it was marketed under brand names like Darvon and Darvocet. In medical form, PPX appeared as tablets or capsules, often pink, orange, or white, depending on formulation. It was taken orally and typically combined with acetaminophen.
Recreationally, propoxyphene was misused for its mild opioid effects, though it was never as powerful or euphoric as stronger opioids. Misuse involved taking higher-than-prescribed doses or crushing and ingesting tablets to intensify sedation. However, PPX also carried significant cardiac risks, including arrhythmias and fatal heart conduction abnormalities, even at therapeutic levels. Because of these dangers, the FDA removed propoxyphene from the U.S. market in 2010, though it may still appear in illicit circulation or older patient supplies.
Despite its discontinuation, PPX remains relevant in toxicology testing because legacy prescriptions, leftover medication, or diversion can still occur. Its presence in a screen may indicate misuse, accidental ingestion, or exposure to outdated pharmaceuticals.
Effects:
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Mild euphoria
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Pain relief and reduced physical discomfort
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Drowsiness and sedation
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Dizziness or lightheadedness
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Nausea or vomiting
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Impaired motor coordination
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Constipation
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Respiratory depression at high doses
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Risk of cardiac conduction abnormalities
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Potential progression to opioid dependence
Commons Slang Terms:
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Speed
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Uppers
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Pep pills
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Bennies
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Dexies
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Go-fast
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Black beauties
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Crank
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Zoomers
Legal Status:
Propoxyphene was classified as a Schedule IV controlled substance under the U.S. Controlled Substances Act before being fully withdrawn from the market. Although it is no longer legally manufactured or prescribed in the U.S., it may still be encountered in toxicology screens because old supplies continue to circulate and may be misused. Its controlled-substance classification historically reflected a lower abuse potential than Schedule II opioids, but its serious cardiac toxicity ultimately led to its removal.
For point-of-care (POC) rapid toxicology testing programs—including workplaces, treatment programs, corrections, and government agencies—PPX may still appear on broader opioid panels. Its inclusion helps programs detect potential misuse of discontinued medications, diversion of older prescriptions, or illicit acquisition. Because PPX should not appear in legitimate medical care today, any confirmed positive generally warrants further investigation. When detected, routine procedure requires laboratory confirmation testing due to cross-reactivity risks and to legally validate results before taking administrative or legal action.
Screening Options:
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