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Does Acid (LSD) Show Up on a Urine Drug Test?

Medically reviewed by Michael O'Connell, DO
Does Acid (LSD) Show Up on a Urine Drug Test?

Key points

  • Effects of LSD: After ingestion, users may experience vivid hallucinations, a distorted sense of time, euphoria, and changes in sensory perception. These effects typically begin 30-90 minutes after ingestion and can last for 8-12 hours. The acute experience is highly dose-dependent and influenced by set (psychological mindset) and setting (environmental context). Common physiological responses during the peak include mild tachycardia, elevated blood pressure, pupillary dilation (mydriasis), increased body temperature, and reduced appetite. While LSD is not associated with classical physical dependence or withdrawal syndromes, repeated use over consecutive days leads to rapid tachyphylaxis, meaning users quickly develop tolerance that requires significantly higher doses to achieve the same effects. This tolerance typically resets after three to seven days of abstinence. Long-term psychological sequelae are rare but documented, most notably Hallucinogen Persisting Perception Disorder (HPPD), which involves recurrent visual disturbances like geometric patterns, halos, or motion trails long after cessation.
  • Legal Status: In the United States and most other countries, LSD is classified as a Schedule I controlled substance. This means it is illegal to manufacture, possess, or distribute, and it has no approved medical use in routine practice. The Schedule I designation reflects both historical regulatory decisions and ongoing federal policy, despite recent scientific interest in controlled therapeutic applications. Research institutions conducting clinical trials must obtain strict DEA Schedule I licenses, utilize FDA Investigational New Drug (IND) approvals, and adhere to rigorous safety protocols.
  • Dosage: LSD is extremely potent, with typical recreational doses ranging from 50-150 micrograms. Because the dose is so small, it is usually applied to a medium like blotter paper ("tabs"), sugar cubes, or gelatin squares for consumption. The active range for perceptual alteration begins at approximately 20 micrograms, while doses exceeding 200 micrograms often produce intense ego dissolution and profound dissociative states. Pharmaceutical-grade purity is impossible to verify in illicit markets, and blotter papers are occasionally adulterated with other research chemicals like NBOMe series compounds, which carry significantly higher toxicity risks and cardiovascular dangers.

Lysergic acid diethylamide (LSD), commonly known as “acid,” is a powerful psychedelic drug famous for its mind-altering effects. If you’re concerned about drug testing—whether for employment, legal, or other reasons—it’s important to understand whether standard screenings can detect LSD. This guide explores how urine drug tests work, how long LSD stays in your system, and answers other frequently asked questions. Understanding the pharmacology of hallucinogens, the technical limitations of standard toxicology screens, and the regulatory frameworks governing workplace testing will help you navigate these concerns with accurate, evidence-based information. As drug testing policies continue to evolve across industries, distinguishing between routine screening protocols and targeted forensic analysis is essential for interpreting potential results correctly and making informed health and professional decisions.

What Is LSD (Lysergic Acid Diethylamide)?

LSD, or “acid,” is a potent hallucinogenic drug known for causing intense changes in perception, mood, and thought. First synthesized in 1938 by Dr. Albert Hofmann from a fungus, its psychedelic properties were discovered in 1943. Pharmacologically, LSD primarily exerts its profound psychoactive effects by acting as a high-affinity partial agonist at serotonin 5-HT2A receptors, particularly within the prefrontal cortex. This receptor activation cascades into downstream modulation of glutamate, dopamine, and norepinephrine pathways, fundamentally altering thalamocortical connectivity and sensory gating. These neurochemical interactions produce the characteristic visual and auditory hallucinations, temporal distortion, emotional lability, and ego dissolution reported by users.

  • Effects of LSD: After ingestion, users may experience vivid hallucinations, a distorted sense of time, euphoria, and changes in sensory perception. These effects typically begin 30-90 minutes after ingestion and can last for 8-12 hours. The acute experience is highly dose-dependent and influenced by set (psychological mindset) and setting (environmental context). Common physiological responses during the peak include mild tachycardia, elevated blood pressure, pupillary dilation (mydriasis), increased body temperature, and reduced appetite. While LSD is not associated with classical physical dependence or withdrawal syndromes, repeated use over consecutive days leads to rapid tachyphylaxis, meaning users quickly develop tolerance that requires significantly higher doses to achieve the same effects. This tolerance typically resets after three to seven days of abstinence. Long-term psychological sequelae are rare but documented, most notably Hallucinogen Persisting Perception Disorder (HPPD), which involves recurrent visual disturbances like geometric patterns, halos, or motion trails long after cessation.
  • Legal Status: In the United States and most other countries, LSD is classified as a Schedule I controlled substance. This means it is illegal to manufacture, possess, or distribute, and it has no approved medical use in routine practice. The Schedule I designation reflects both historical regulatory decisions and ongoing federal policy, despite recent scientific interest in controlled therapeutic applications. Research institutions conducting clinical trials must obtain strict DEA Schedule I licenses, utilize FDA Investigational New Drug (IND) approvals, and adhere to rigorous safety protocols.
  • Dosage: LSD is extremely potent, with typical recreational doses ranging from 50-150 micrograms. Because the dose is so small, it is usually applied to a medium like blotter paper ("tabs"), sugar cubes, or gelatin squares for consumption. The active range for perceptual alteration begins at approximately 20 micrograms, while doses exceeding 200 micrograms often produce intense ego dissolution and profound dissociative states. Pharmaceutical-grade purity is impossible to verify in illicit markets, and blotter papers are occasionally adulterated with other research chemicals like NBOMe series compounds, which carry significantly higher toxicity risks and cardiovascular dangers.

How Do Urine Drug Tests Work?

To understand if LSD appears on a drug test, it helps to know how these tests function. Urine drug screens, or urinalysis, are common methods for detecting recent drug use. They work by identifying metabolites—the breakdown products of drugs—that are excreted in urine. From a toxicological perspective, understanding drug metabolism and renal excretion is essential. After ingestion, LSD is absorbed primarily through the gastrointestinal mucosa, though sublingual or transdermal routes are occasionally utilized. It undergoes extensive first-pass metabolism in the liver, predominantly mediated by the cytochrome P450 enzyme family, particularly CYP2D6, CYP3A4, and CYP1A2. The parent compound has an elimination half-life of approximately 3.5 to 4 hours in healthy adults. Hepatic pathways convert LSD into multiple hydroxylated and demethylated metabolites, with 2-oxo-3-hydroxy-LSD (O-H-LSD) being the primary urinary excretion product. These water-soluble compounds are then filtered by the glomeruli and secreted into the renal tubules before final elimination.

Most initial screenings use an immunoassay, which uses antibodies designed to react to specific drugs or their metabolites. If a substance is detected above a certain "cut-off level," the result is a presumptive positive. Immunoassays like enzyme-multiplied immunoassay technique (EMIT), cloned enzyme donor immunoassay (CEDIA), and fluorescence polarization immunoassay (FPIA) are optimized for high-throughput processing, providing rapid, cost-effective preliminary results. However, these assays rely on competitive binding principles and can occasionally cross-react with structurally similar compounds, prescription medications, or dietary supplements. If an initial screen is positive, the sample is sent for a more precise confirmatory test, typically gas chromatography-mass spectrometry (GC-MS) or liquid chromatography-tandem mass spectrometry (LC-MS/MS), which can identify specific molecules with high accuracy. Confirmatory testing separates complex mixtures via chromatography before ionizing the compounds and measuring their mass-to-charge ratios against certified reference standards. This two-tiered methodology is mandated by clinical laboratory guidelines and federal workplace regulations to ensure analytical specificity and prevent false reporting.

Standard Drug Testing Panels

Most drug tests screen for a standard set of commonly abused substances. These are often named for the number of substances they detect.

Standard Drug Test Panel Typical Substances Screened
5-Panel Test Marijuana (THC), Cocaine, Opiates (e.g., heroin, morphine), Amphetamines (e.g., meth), and Phencyclidine (PCP)
7-Panel Test Includes all 5-Panel substances, plus Barbiturates and Benzodiazepines (e.g., Xanax, Valium)
10-Panel Test Includes all 7-Panel substances, plus Methadone, Propoxyphene, and Methaqualone (Quaaludes)
12-Panel Test Includes all 10-Panel substances, plus extended opiates (e.g., oxycodone) and other drugs like MDMA (Ecstasy)

Crucially, LSD is rarely included in these standard panels. Testing for it requires specialized methods that are not part of routine screenings. The absence of classic hallucinogens from these configurations is a deliberate policy choice driven by epidemiological data, cost-efficiency, and regulatory guidelines established by organizations like SAMHSA and the Department of Transportation (DOT). Federal mandates prioritize substances that pose immediate public safety risks, demonstrate high addiction potential, or show widespread occupational prevalence. Private employers typically adopt similar panels to maintain testing affordability, streamline laboratory logistics, and ensure compliance with standard workplace drug-free policies. Customizing a panel to include LSD or other psychedelics requires explicit employer authorization, specialized laboratory contracts, and additional funding for targeted assays.

Does LSD (Acid) Show Up on a Standard Urine Drug Test?

The short answer is no. LSD will typically not show up on a standard urine drug test, such as the common 5-panel or 10-panel screens used by most employers. These tests are not designed to detect LSD.

There are several key reasons why LSD isn't included in standard tests:

  • Low Prevalence of Use: LSD is used less frequently than substances like marijuana or opioids, so employers and testing programs prioritize more common drugs. National survey data consistently places hallucinogen use well below stimulants, depressants, and cannabinoids, making routine screening statistically inefficient.
  • Detection Difficulty: LSD is active at extremely low doses (in micrograms), and the body metabolizes it quickly. This means the concentration of LSD and its metabolites in urine is often too low for standard tests to detect. Standard immunoassay cartridges lack the sensitivity to reliably capture picogram-level concentrations without significant false-negative rates.
  • Cost and Complexity: Testing for LSD requires specialized, more expensive equipment and procedures. Adding it to a routine panel would significantly increase the cost. High-throughput automated analyzers used in commercial labs are calibrated for common metabolites; reconfiguring them for hallucinogen detection disrupts workflow and increases per-test pricing.
  • Instability of the Compound: LSD can degrade when exposed to heat or light, making it challenging to get a reliable result if a sample is not stored properly. The molecule is sensitive to ultraviolet radiation, oxidative environments, and extreme pH levels, which complicates transport, storage, and laboratory analysis unless strict cold-chain protocols are maintained.

In summary, a person who has taken LSD is highly unlikely to test positive on a standard workplace drug screen unless the test has been specifically ordered to include LSD. Beyond technical constraints, workplace drug testing functions primarily as a risk-management tool rather than a comprehensive toxicological audit. Employers focus on detecting substances that demonstrably impair psychomotor coordination, judgment, or safety awareness during work hours. While LSD produces profound cognitive alterations, its short duration of action, unpredictable usage patterns, and lack of classical withdrawal symptoms make it a lower priority for occupational screening programs compared to alcohol, benzodiazepines, or prescription stimulants. Consequently, unless a company mandates a custom forensic panel following a specific workplace incident, accident investigation, or court order, routine employment screenings will bypass hallucinogen detection entirely.

Specialized LSD Drug Testing

While not part of standard panels, it is possible to test for LSD with specialized drug tests. These tests may be used in specific situations, such as forensic investigations, court-ordered monitoring, addiction treatment programs, or for certain high-security jobs requiring comprehensive background clearances.

  • LSD-Specific Immunoassay: Some labs offer an initial screening test designed specifically for LSD and its main metabolite, 2-oxo-3-hydroxy-LSD (O-H-LSD). These assays utilize monoclonal antibodies calibrated to bind selectively to the hallucinogen's metabolic byproducts. Laboratories offering this service typically require advance scheduling and specific chain-of-custody documentation to ensure legal defensibility.
  • Confirmatory Tests (GC-MS or LC-MS/MS): These are the gold-standard methods for confirming LSD use. They are highly accurate and can detect even tiny concentrations of the drug in urine. GC-MS separates volatile derivatives of the metabolites before ionizing them, while LC-MS/MS handles the compounds in liquid phase without extensive derivatization. LC-MS/MS is increasingly favored due to its superior sensitivity (reaching low picogram-per-milliliter thresholds), faster turnaround, and enhanced ability to quantify multiple analytes simultaneously. Confirmatory testing must meet strict Clinical Laboratory Improvement Amendments (CLIA) certification and College of American Pathologists (CAP) accreditation standards to withstand forensic scrutiny.

When a specialized LSD panel is ordered, the analytical workflow follows stringent quality assurance protocols. Samples undergo initial validity checks measuring temperature, creatinine concentration, specific gravity, pH, and oxidant markers to rule out adulteration, substitution, or dilution. If the specimen passes validity criteria, it proceeds to immunoassay screening. A presumptive positive automatically triggers reflex confirmation via mass spectrometry. The laboratory then calculates precise metabolite-to-creatinine ratios to normalize results against individual hydration status. The final report is reviewed by a board-certified pathologist or toxicologist before being transmitted to the requesting authority, ensuring clinical accuracy and legal compliance throughout the process.

Detection Window for LSD in Urine

Even with specialized tests, LSD has a relatively short detection window compared to many other drugs.

  • Typical Use: After a single dose, LSD is typically detectable in urine for 24 to 48 hours. Renal clearance is efficient, and metabolites rarely persist beyond two days in healthy individuals with normal hepatic and renal function.
  • High Doses or Frequent Use: With higher doses, some advanced tests may detect LSD metabolites for up to 72 hours (3 days). Saturation of metabolic enzymes and prolonged tissue redistribution can marginally extend the excretion phase, though classical hallucinogens do not accumulate in adipose tissue like cannabinoids.
  • Microdosing: Taking very small, sub-perceptual doses of LSD (typically 5-20 micrograms) is highly unlikely to be detected by any test, though frequent (daily) use could theoretically lead to a build-up of metabolites detectable by the most sensitive tests for a short period. Even with aggressive microdosing protocols, urinary concentrations usually remain below established clinical cutoff thresholds, particularly when accounting for standard dilution from normal fluid intake.

Urine pH significantly influences detection timelines. LSD and its metabolites are weakly basic compounds, meaning they exhibit enhanced renal reabsorption in alkaline environments and accelerated elimination in acidic urine. However, intentionally altering systemic pH through dietary manipulation or supplement consumption carries medical risks, including electrolyte imbalances, metabolic alkalosis, and kidney stress. Clinical toxicology literature emphasizes that natural metabolic rates, rather than artificial modification, dictate the actual window of detection.

Factors That Affect How Long LSD Stays in Your System

Several individual factors can influence how long LSD remains detectable:

  • Dosage: Higher doses of LSD will take longer for the body to process and eliminate. Pharmacokinetic clearance follows zero-order kinetics only at extreme saturating doses; otherwise, elimination proceeds predictably based on hepatic enzyme capacity.
  • Frequency of Use: Frequent use may lead to accumulation, potentially extending the detection window slightly. Though LSD lacks significant lipid solubility for fat storage, repeated daily administration can transiently overwhelm phase I and phase II metabolic pathways.
  • Individual Metabolism: Factors like age, liver function, body mass, and overall health affect how quickly your body metabolizes LSD. Genetic polymorphisms in CYP2D6 and CYP3A4 enzymes dictate inter-individual variability in drug clearance rates, creating "poor metabolizers" who retain substances longer than "extensive metabolizers."
  • Hydration: While staying hydrated may dilute urine, attempting to "flush" your system by drinking excessive water is not a reliable method and can lead to a sample being rejected as invalid. Laboratories routinely flag diluted specimens by measuring creatinine (<20 mg/dL) and specific gravity (<1.003). A reported negative-dilute result often triggers mandatory retesting under direct observation.
  • Test Sensitivity: Highly sensitive lab tests (like LC-MS/MS) can detect much smaller amounts of LSD than standard screening assays. Cutoff concentrations vary by laboratory protocol and legal jurisdiction; forensic labs often utilize lower thresholds than workplace compliance programs, extending the theoretical detection window.
  • Concurrent Medication Use: Prescription drugs, particularly cytochrome P450 inhibitors (e.g., fluoxetine, ritonavir, cimetidine) or inducers (e.g., rifampin, carbamazepine), can competitively alter LSD metabolism, either prolonging or accelerating clearance. Over-the-counter supplements, particularly grapefruit extract and St. John’s Wort, similarly modulate hepatic enzyme activity.
  • Organ Function Impairment: Pre-existing hepatic cirrhosis, chronic kidney disease, or heart failure significantly reduce drug clearance efficiency. Compromised glomerular filtration rates (GFR) or diminished hepatic blood flow directly prolong the presence of parent compounds and metabolites in biological fluids.

Understanding these physiological variables is crucial for medical professionals interpreting toxicology reports. Drug testing is a probabilistic assessment rather than an absolute measurement, and clinical context must always accompany analytical results.

LSD and Different Types of Drug Tests

While urine tests are most common, LSD's detectability varies in other types of screenings.

  • Blood Tests: LSD is detectable in blood for only a short period, usually up to 6-12 hours after use. Blood tests are rare and typically only used in emergency or forensic situations. Plasma concentrations peak within 1.5 to 3 hours post-ingestion, correlating closely with subjective psychoactive effects. Clinicians utilize serum testing in overdose scenarios to assess toxicity severity, manage cardiovascular instability, or guide symptomatic treatment protocols.
  • Saliva Tests: Saliva testing for LSD is also uncommon. The detection window is short, likely around 24 hours. Oral fluid testing has expanded for roadside DUI enforcement and workplace compliance due to non-invasive collection and reduced adulteration risk. However, commercially available oral fluid immunoassays rarely include validated hallucinogen cartridges, and low drug concentrations in saliva complicate reliable detection.
  • Hair Follicle Tests: In theory, hair tests can detect drug use for up to 90 days. However, because LSD is taken in such small doses, very little is incorporated into the hair, making detection difficult and unreliable. Hair testing for LSD is extremely rare. Drugs must enter the bloodstream, diffuse into dermal capillaries, and bind to the keratin matrix in the hair follicle to become detectable. LSD's hydrophilic metabolites and microgram dosing result in negligible incorporation rates. External contamination from handling blotter papers or environmental exposure further complicates interpretation, requiring rigorous washing protocols and metabolite-to-parent-drug ratio analysis that few commercial laboratories offer. Sweat patch monitoring offers an alternative long-term matrix, but standardized cutoff values and contamination controls remain inadequately established for hallucinogens in forensic guidelines.

Can LSD Use Trigger a False Positive for Other Drugs?

A common concern is whether taking one drug can cause a false positive for another. LSD's chemical structure is unique, so it will not cause a false positive for other drugs on a standard panel, such as amphetamines, benzodiazepines, or opiates. The antibody specificity in standard workplace immunoassays is highly selective for these distinct pharmacological classes, and structural cross-reactivity between LSD and common drugs of abuse is virtually nonexistent.

However, some medications have been reported to cause a false positive on an LSD-specific screen. These include certain antidepressants like sertraline (Zoloft), trazodone, tricyclic antidepressants, and some over-the-counter antihistamines like diphenhydramine or chlorpheniramine. This is why any initial positive screening result must be confirmed with a more accurate method like GC-MS to rule out a false positive. When a presumptive positive occurs, the sample undergoes Medical Review Officer (MRO) evaluation. The MRO, a licensed physician with specialized training in toxicology, contacts the individual to verify prescription status, review medical history, and assess potential interfering substances. Only after ruling out legitimate medical explanations and confirming the result via mass spectrometry is a final positive reported to the requesting authority. This multi-step verification process effectively eliminates analytical errors and protects individuals from unwarranted administrative or legal consequences.

Key Takeaways

  • LSD is not included in standard urine drug test panels and will not show up on most routine screenings for employment.
  • Specialized tests are required to detect LSD, but these are expensive and not commonly used.
  • LSD has a short detection window in urine, typically 24-48 hours, and rarely more than 3 days.
  • The small dosage, rapid metabolism, and chemical instability of LSD make it difficult to detect.
  • The only guaranteed way to pass a drug test is to abstain from using the substance.

Additional Resources

For more information on LSD and drug testing, consult these reputable sources:

Frequently Asked Questions

Can drinking large amounts of water guarantee a negative result for LSD?

No. While excessive hydration can temporarily dilute urine concentrations, modern laboratory protocols routinely measure specimen validity markers including creatinine, specific gravity, pH, and temperature. If these parameters fall outside established reference ranges, the sample is flagged as dilute or invalid. Most employers and testing programs mandate a repeat collection, often under direct observation, to prevent evasion attempts. Furthermore, consuming extreme volumes of water rapidly can precipitate acute hyponatremia, leading to dangerous electrolyte imbalances, cerebral edema, seizures, and potentially fatal neurological complications. Medical professionals strongly advise against attempting to manipulate urine chemistry, as it poses serious health risks and typically fails to circumvent standardized laboratory quality control measures.

Will a standard pre-employment screening ever accidentally include LSD without my employer requesting it?

Highly unlikely. Commercial toxicology laboratories operate using strict panel configurations explicitly authorized by the employer. Immunoassay cartridges are pre-loaded with specific antibody targets corresponding to the requested panel (5-panel, 10-panel, etc.). Adding unplanned analytes disrupts automated workflow, increases reagent costs, and violates contractual testing agreements. Furthermore, laboratory accreditation standards prohibit unauthorized testing beyond the ordered parameters to maintain chain-of-custody integrity and billing transparency. Unless your employer specifically contracts for a comprehensive forensic toxicology workup or explicitly adds an LSD screen as a customized module, routine employment testing will exclusively analyze for the designated substances listed in your company's drug-free workplace policy.

How do employers or probation officers request LSD testing specifically?

Specialized testing requires a direct order through a certified reference laboratory that offers hallucinogen panels. The requesting authority must complete specific requisition forms indicating the need for LSD or expanded drug screening, acknowledge the additional costs, and establish proper chain-of-custody documentation. These requests are typically reserved for forensic investigations, court-ordered substance abuse monitoring, specific workplace incidents involving erratic behavior, or high-security clearance applications. The laboratory then configures its analytical workflow to include LSD-specific immunoassay screening followed by mandatory LC-MS/MS confirmation. Results are transmitted exclusively to the authorized party through secure, encrypted channels, with a Medical Review Officer available to interpret findings and address any prescription-related interferences before finalizing the report.

Does microdosing LSD increase the risk of detection compared to single recreational doses?

Generally, no. Microdosing involves ingesting sub-perceptual amounts, typically ranging from 5 to 20 micrograms, which are significantly below standard recreational thresholds. Because the administered quantity is so low, the resulting concentration of urinary metabolites typically falls beneath the analytical cutoff limits of even highly sensitive LC-MS/MS assays. However, theoretical detection risk increases marginally with chronic, daily administration due to transient metabolic pathway saturation, particularly in individuals with slower genetic metabolism profiles or compromised renal function. Despite this, published clinical toxicology studies indicate that microdosing protocols rarely produce positive results within standard testing parameters. Nevertheless, any use of a Schedule I controlled substance carries legal risks, and laboratory detection capabilities continue to improve as analytical chemistry advances.

What happens if my drug test comes back positive for LSD?

If a specialized test yields a positive result, standard protocol dictates immediate reflex confirmation via GC-MS or LC-MS/MS to verify the initial finding. The specimen and results are then forwarded to a board-certified Medical Review Officer (MRO), who contacts you directly to review potential medical explanations, prescription histories, or over-the-counter medications that might interfere with the assay. If a legitimate prescription or documented medical condition accounts for the result, the MRO may report it as a verified negative or medically justified exception. If no valid medical explanation exists and confirmation testing validates the presence of LSD metabolites, the positive result is reported to the requesting employer or legal authority. Consequences vary by jurisdiction and policy, potentially including mandatory counseling, suspension, termination, or legal penalties. You typically have the right to request a retest of the original specimen within a specified timeframe (usually 72 hours to 7 days) and may consult legal counsel regarding workplace rights and regulatory compliance.

Are there FDA-approved medications used to treat LSD intoxication or severe adverse reactions?

There are no medications specifically FDA-approved for treating LSD intoxication, but emergency medical management focuses on supportive care and symptom stabilization. Clinicians typically place patients in a calm, low-stimulation environment ("talking down" or verbal reassurance) to mitigate acute anxiety, paranoia, or panic attacks. In cases of severe agitation, aggression, or cardiovascular instability, benzodiazepines such as lorazepam or diazepam are first-line pharmacological interventions. These agents enhance GABAergic inhibition, reducing sympathetic overdrive, lowering blood pressure, calming psychomotor agitation, and alleviating psychological distress without exacerbating psychedelic symptoms. Antipsychotics like haloperidol are generally avoided unless absolutely necessary, as they can lower seizure thresholds or interact unpredictably with serotonergic pathways. Emergency department protocols prioritize monitoring vital signs, ensuring patient safety from accidental injury during altered perceptual states, and providing hydration until the drug naturally clears the system, which typically occurs within 8 to 12 hours post-ingestion.

Disclaimer: This article is for informational purposes only and does not constitute medical or legal advice. If you have concerns about substance use or drug testing, please consult a qualified healthcare professional or legal expert.

Michael O'Connell, DO

About the author

Emergency Medicine Physician

Michael O'Connell, DO, is a board-certified emergency medicine physician working as an attending physician at a busy Level I Trauma Center in Philadelphia, Pennsylvania. He also serves as a clinical instructor for medical residents and is active in wilderness medicine.