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Accredited Drug Testing provides extensive drug and alcohol evaluations at 40 testing centers in the South Fulton, Tennessee vicinity. Our offerings include DOT and non-DOT urine drug screenings, breath alcohol tests, EtG alcohol analyses, and hair drug screenings, catering to individuals, employers, and legal requirements. In South Fulton, TN, we provide speedy result testing and SAMSA certified laboratory analyses. Most testing sites are conveniently located close to your residence or workplace. Additional services we provide consist of Occupational Health Examinations, Clinical Testing, and Background Verifications.
Reach out at (800) 221-4291 or sign up online. Choose your desired test and select a nearby site—testing services are available for you, your employees, or others. Arranging a test is Quick and Simple; contact our scheduling team or book your test via our online platform available 24/7. Our efficient and intuitive system lets you set up drug screenings near South Fulton with ease.
* 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 South Fulton 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.
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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 South Fulton, located in Obion County, drug overdose deaths increased by 15% from the previous year, highlighting a growing concern in the community.
Obion County, which includes South Fulton, reported that opioids were involved in approximately 70% of the drug-related fatalities in the most recent report.
The South Fulton area saw a 25% increase in methamphetamine-related arrests over the past year, according to local law enforcement statistics.
Local treatment centers in South Fulton, Obion County, noted a rise in the number of individuals seeking assistance for prescription drug abuse.
In Obion County schools, surveys revealed that 20% of high school students admitted to recreational drug use in the past year.
Emergency calls related to drug overdoses in South Fulton, TN, surged by 30% in recent months, indicating an alarming trend.
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 South Fulton, TN, are increasingly adopting drug testing policies to maintain safe and productive workplaces. These policies often include pre-employment screenings and random drug tests to deter substance abuse among employees. Many local businesses adhere to guidelines set by the Occupational Safety and Health Administration (OSHA), ensuring compliance with federal standards for workplace safety.
Additionally, employers may collaborate with the Tennessee Department of Labor and Workforce Development (TDLWD) to offer support and resources for employees struggling with addiction. By providing access to counseling and rehabilitation services, companies demonstrate their commitment to fostering a supportive work environment.
In response to rising drug-related issues, South Fulton, TN, has implemented several strategies in collaboration with state and federal agencies. The Tennessee Department of Health (TDH) has launched campaigns to increase public awareness and provide resources for addiction recovery. These initiatives aim to curb the growing problem of substance abuse in the community.
Moreover, local government efforts include partnerships with the Tennessee Bureau of Investigation (TBI) to combat drug trafficking. South Fulton's police force is continuously trained to address drug-related incidents effectively through state-sponsored programs, ensuring a safer environment for residents.
Recent drug busts in South Fulton, TN, highlight ongoing efforts to combat illegal drug activities in the area. In a significant operation, local law enforcement, in coordination with state authorities, successfully dismantled a methamphetamine trafficking ring, resulting in several arrests. This operation underscores the persistent challenges law enforcement faces in curbing drug distribution networks.
Drug-related events in the community often involve coordinated responses from multiple agencies. For instance, a recent collaboration between the South Fulton Police Department and the Drug Enforcement Administration (DEA) led to the seizure of substantial quantities of illegal substances, disrupting the supply chain in the region.
Accredited Drug Testing offers fast, reliable employment screening services in South Fulton, TN. Trusted by employers nationwide for accurate results and exceptional service.
Tennessee DOT/Non DOT Physicals
Tennessee Association of Alcohol, Drug & Other Addiction Services
National Association of Drug Court Professionals
Tennessee Prescription Drug Drop Box Program
Driving Innovation to Decisions Institute, Inc
Tennessee Department of Mental Health & Substance Abuse Services
Tennessee Recovery Network
Resources for Community Support, Inc.
Tennessee Bureau of Investigation Statistics
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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