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At Accredited Drug Testing, we deliver extensive drug and alcohol testing solutions across our 38 centers in the Atwood, Tennessee vicinity. Our offerings include DOT and non-DOT urine drug screenings, breath alcohol assessments, EtG alcohol tests, and hair drug analyses for personal, employment, and legal purposes. Our Atwood, TN services promise quick-result testing coupled with SAMSA certified lab exams. Many Atwood testing spots are conveniently positioned close to your residence or workplace, providing same-day services. We also conduct Occupational Health Screenings, Clinical Testing, and offer Background Checks.
Reach out at (800) 221-4291 or register via our website. Selecting a test and a nearby Atwood location is simple—tests are available for individuals, employees, or others. The test scheduling process is quick and straightforward; contact our scheduling team or arrange your test online any time. Our efficient and intuitive system ensures smooth drug testing arrangements near Atwood.
* 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 Atwood 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
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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 Carroll County, which includes Atwood, TN, drug overdose deaths have increased by 25% over the past five years.
Atwood, TN, reported a rise in methamphetamine-related incidents according to a 2022 Carroll County health report.
The annual drug abuse report noted that 15% of drug arrests in Carroll County involved opiates in 2021.
Surveys from 2021 indicate that approximately 12% of Atwood's youth have experimented with illegal substances.
Carroll County's drug rehabilitation centers saw a 30% increase in demand for services in 2020 compared to previous years.
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 Atwood, TN, are increasingly adopting stringent drug testing policies to ensure a safe and productive work environment. Many local businesses adhere to the guidelines set by the Tennessee Department of Labor and Workforce Development, which provides frameworks for workplace drug testing procedures.
Random drug testing and pre-employment screening have become standard practices among several large employers in Atwood. These measures are intended not only to maintain a drug-free workplace but also to support employees in seeking help for substance abuse through Employee Assistance Programs (EAPs).
The government of Atwood, TN, along with Carroll County officials, has launched several initiatives to combat the growing drug problem in the region. This includes collaborating with the Tennessee Government's Mental Health and Substance Abuse Services to provide better access to treatment programs. The introduction of community outreach programs and educational workshops aims to raise awareness about the dangers of drug abuse.
Additionally, the local government's collaboration with state agencies has facilitated the provision of more resources for the town's law enforcement, enhancing their capabilities to tackle drug-related crimes. For more information about their efforts, you can visit the Tennessee Department of Safety and Homeland Security.
In recent years, several notable drug busts have occurred in Atwood, TN, reflecting the ongoing battle against substance abuse in the area. One significant operation in 2023 led to the arrest of multiple individuals involved in a methamphetamine distribution network operating within Carroll County. The successful bust was a collaborative effort between local law enforcement and the Drug Enforcement Administration (DEA).
The heightened law enforcement activity has led to an increase in community awareness and has highlighted the importance of continued vigilance and cooperation between residents and authorities.
Accredited Drug Testing offers fast, reliable employment screening services in Atwood, TN. Trusted by employers nationwide for accurate results and exceptional service.
Tennessee DOT/Non DOT Physicals
Tennessee Department of Mental Health and Substance Abuse Services
Tennessee o-drug Crisis Response
Tennessee Department of Human Services - Substance Abuse
Tennessee Bureau of Investigation - Drug Investigation Division
Council on Alcohol & Drug Abuse
Tennessee Coalition to End Domestic and Sexual Violence
Carroll County Drug Court
Centerstone
New Directions for Wellness
Mid-South Substance Abuse
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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