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At our 34 locations in the Hampton, Tennessee region, Accredited Drug Testing provides all-encompassing drug and alcohol testing services. Our offerings include DOT and non-DOT urine drug testing, breath alcohol tests, EtG alcohol assessments, and hair follicle drug tests suitable for personal, employer, and legal use. Conveniently, our Hampton, TN facilities provide quick-result services and SAMSA certified lab evaluations. Most testing centers are easily accessible from your home or workplace. We also provide Occupational Health Testing, Clinical Testing, and Background Checks.
Contact us at (800) 221-4291 or register online. To arrange a test, select your preferred test and nearby site—available for personal, employee, or third-party testing. Scheduling is quick and straightforward; contact our scheduling team or arrange your test online at any time. Our seamless and intuitive process ensures you can set up drug testing near Hampton without hassle.
* You must register by phone or online to receive your donor pass/registration prior to proceeding to the testing center. You must bring a valid government issued ID along with the registration/barcode number which was sent to you by email.
When you're searching for drug testing near me or drug testing locations, we provide a simple and convenient process to find a drug and alcohol testing location near you that is certified to provide all of your drug and alcohol testing needs.
At our Hampton drug testing collection sites, Accredited Drug Testing provides one of the widest selections of drug and alcohol testing services available. Whether you're an employer, attorney, court, or private individual, we offer both DOT and non-DOT testing options—ranging from rapid tests to comprehensive lab-based screenings—capable of detecting nearly any substance.
DOT Drug Testing and Requirements
DOT Employer Drug Policy Development
If you're an employer needing to test 25 or more employees and looking to save time and money, we offer mobile on-site drug testing where we come to you. Call us today for more information.
In 2021, Hampton, TN experienced a 15% increase in drug-related offenses compared to the previous year within Carter County.
Carter County, which includes Hampton, reported over 120 opioid overdose cases in 2022.
Methamphetamine is identified as the most commonly abused drug in Carter County, with Hampton being a major area of concern.
In Carter County, 25% of high school students have reported using illegal substances in a 2022 survey.
The rate of drug-related emergency room visits in Carter County, including Hampton, has increased by 10% from 2020 to 2022.
Hampton, TN, sees a high rate of prescription drug misuse, with Carter County's rates 10% above the state average.
Drug elimination is the sum of the processes of removing an administered drug from the body. In the pharmacokinetic ADME scheme (absorption, distribution, metabolism, and excretion), it is frequently considered to encompass both metabolism and excretion. Hydrophobic drugs, to be excreted, must undergo metabolic modification making them more polar. Hydrophilic drugs, on the other hand, can undergo excretion directly, without the need for metabolic changes to their molecular structures.
Although many sites of metabolism and excretion exist, the chief organ of metabolism is the liver, while the organ primarily tasked with excretion is the kidney. Any significant dysfunction in either organ can result in the accumulation of the drug or its metabolites in toxic concentrations.
A variety of other factors impact elimination — intrinsic drug properties, such as polarity, size, or pKa. Also other factors include genetic variation among individuals, disease states affecting other organs, and pathways involved in the way the drug distributes through the body, such as first-pass metabolism.
Drug elimination is the removal of an administered drug from the body. It is accomplished in two ways, either by excretion of an unmetabolized drug in its intact form or by metabolic biotransformation followed by excretion. While excretion is primarily carried out by the kidneys, other organ systems are involved as well. Similarly, the liver is the primary site of biotransformation, yet extrahepatic metabolism takes place in a variety of organ systems affecting multiple drugs.
Given the multiple organ systems and the variety of metabolic transformations present, drug elimination can entail a significant degree of complexity. Hydrophilic drugs are typically directly excreted by the kidneys, while hydrophobic drugs undergo biotransformation before excretion. The purpose here is twofold – biotransformation serves both detoxify the exogenous substances as well as to increase their hydrophilicity, ensuring their elimination via the kidneys.
Two broad metabolic pathways of hepatic drug transformation exist. Phase I is the direct modification of the target molecule, whereas phase II entails conjugation of the target to a polar molecule of low molecular weight. Phase I prepare the drug to enter phase II, but single-phase metabolism also exists.
Phase I involves oxidation, reduction, and hydrolysis of the exogenous molecule. These reactions are accomplished by hepatic microsomal enzymes, which reside in the smooth endoplasmic reticulum of the hepatocytes. Best known among them is the cytochrome P450 system, whose enzymes are predominantly involved in oxidative metabolism. Within the cytochrome P450 family (CYP), the enzyme responsible for the metabolism of more than 50% of existing drugs is the CYP3A4. Its activity encompasses various classes of medications, including opioids, immunosuppressants, antihistamines, and benzodiazepines. The enzymes can also be induced or inhibited by a variety of substances they interact with, including pharmaceuticals. The increase in metabolic activity with CYP induction results in a diminished activity of drugs targeted by that particular isoform. Conversely, CYP inhibition will result in increased drug plasma concentration, potentially leading toxicity. The CYP3A4 is induced by phenytoin, phenobarbital, and St. John's wort, while diltiazem, erythromycin, and grapefruit inhibit it. Caution is, therefore, necessary when administering CYP3A4-metabolized drugs in the presence of any of the inhibitors or inducers.
Phase II consists of covalent bonding of polar groups to nonpolar molecules to render them water-soluble and allow renal or biliary excretion. Target molecules enter phase II directly or via initial processing through phase I. A variety of polar adjuncts is transferred, including amino acids, glucuronic acid, glutathione, acetate, and sulfate. Glucuronidation is one of the major pathways of phase II biotransformation. The UDP-glucuronosyltransferase (UGT) enzyme family performs this activity. Typically, glucuronide derivatives possess less or no activity of the original drug, but in some cases, pharmacologically active compounds result. Morphine-6-glucuronide is a phase II metabolite of morphine with significant analgesic activity. As with the CYP enzymes, inducers, and inhibitors of phase II, enzymes exist and may influence the efficacy of drugs that rely on conjugation before excretion.
The first-pass effect is a feature of hepatic metabolism that also plays a role in the elimination of multiple drugs. Here, the enteric consumed drugs are exposed directly to the liver via the portal vein, where they undergo biotransformation before entering the systemic circulation. This activity reduces the bioavailability and needs to be factored into the dose administered to the patient. Intravenously administered drugs are not subject to the first-pass effect.
Extrahepatic drug metabolism takes place in the GI tract, kidneys, lungs, plasma, and skin.
Renal excretion completes the process of elimination that begins in the liver. Polar drugs or their metabolites get filtered in the kidneys and typically do not undergo reabsorption. They subsequently get excreted in the urine. Urinary pH has a significant impact on excretion, as drug ionization changes depending on the alkaline or acidic environment. Increased excretion occurs with weakly acidic drugs in basic urine and weakly basic drugs in acidic urine.
Excretion in the bile is another significant form of drug elimination. The liver can actively secrete ionized drugs with a molecular weight greater than 300 g/mol into bile, from where they reach the digestive tract and are either eliminated in feces or reabsorbed as part of the enterohepatic cycle.
Other pathways of excretion include the lungs, breast milk, sweat, saliva, and tears
Employers in Hampton, TN, have implemented strict drug testing policies as part of their commitment to maintaining a drug-free workplace. These policies include pre-employment screening, random testing, and post-accident testing to ensure workplace safety and productivity.
Many of the local businesses actively participate in the Tennessee Drug-Free Workplace Program, which provides guidelines and resources for establishing comprehensive drug testing policies. Employers are encouraged to utilize resources from the Tennessee Department of Labor and Workforce Development to aid in policy implementation.
The increased emphasis on such policies reflects the broader community effort in Hampton, TN, to address the growing impact of drug abuse on the local economy and workforce. Businesses support employees seeking treatment and rehabilitation for substance abuse issues, contributing to a healthier workplace environment.
The government has been taking active measures to combat the drug problem in Hampton, TN, as part of Carter County through the allocation of resources to enhance rehabilitation programs. One major initiative focuses on community outreach and education to reduce drug abuse and prevent addiction.
Federal, state, and local agencies are working in tandem to provide better support for law enforcement efforts aimed at curbing drug distribution. Organizations like Tennessee Department of Mental Health and Substance Abuse Services offer programs to support affected individuals.
Recent drug busts in Hampton, TN, have spotlighted the ongoing challenges law enforcement faces in tackling drug distribution networks. In a notable case last year, the Carter County Sheriff's Office conducted a large operation resulting in multiple arrests and the seizure of significant quantities of methamphetamine.
Such operations are often the result of collaborative efforts between local law enforcement and federal agencies like the DEA, showcasing the effectiveness of combined resources in combating drug crimes. These events underscore the need for continued vigilance and community cooperation to reduce drug-related activities in the area.
The local community remains engaged through neighborhood watch programs and public forums aimed at educating residents about the dangers and warning signs of drug activity, further demonstrating the communal effort to fight the ongoing drug crisis in Hampton, TN.
Accredited Drug Testing offers fast, reliable employment screening services in Hampton, TN. Trusted by employers nationwide for accurate results and exceptional service.
Tennessee DOT/Non DOT Physicals
Tennessee Department of Mental Health
Tennessee o-drug Response
Partnership for Drug-Free Kids TN
Carter County Drug Prevention
Suicide Prevention in Tennessee
Chattanooga Drug-Free Coalition
Partnership to End Addiction
Drug Rehab Headquarters TN
JACOA
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Trish last week and Tatiana this week, very fun and easy folks to deal with. Well be using them more and more in the future.
Tom O - 12/19/2024
Trish was amazing and got me through the sytem very fast and swift. I had a hard time hearing her a couple of times, but she was super sweet and helpful throughout the process. Highly recommend her!
Sophia Schutze - 6/19/2024
I've had to use this service twice for out of state physicians we've hired and both times it was super easy. Both customer service reps I spoke with were super helpful and courteous. I won't hesitate to use their service again if needed.
Alicia Rau - 6/19/2024