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Accredited Drug Testing provides a complete suite of drug and alcohol screening solutions at our 35 testing centers located in the Saint George, South Carolina region. Our offerings include DOT-compliant and non-DOT urine drug tests, breath alcohol analyses, EtG alcohol screens, and hair follicle drug assessments, catering to individuals, employers, and legal requisites. In Saint George, SC, we ensure quick test results and utilize SAMSA-certified lab audits. With services available the same day, most Saint George testing sites are conveniently situated close to residences or workplaces. We also offer testing for occupational health, clinical purposes, and conduct background verifications.
To schedule a test, call (800) 221-4291 or register on our website. Choose your desired test and find a location nearby—testing is accessible for personal, employee, or third-party requirements. With Fast and Easy scheduling, contact our scheduling team or arrange your test online at any time. Our efficient, easy-to-navigate system ensures seamless drug testing arrangements near Saint George.
* 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 Saint George 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.
As of 2021, Dorchester County, which includes Saint George, SC, noted an increase in opioid-related overdoses by 25%.
Saint George, SC, part of Dorchester County, reported 15 drug-related arrests in the first half of 2021.
In 2020, Dorchester County had a drug-induced mortality rate of 19 per 100,000 residents.
Saint George, SC saw a 30% increase in drug-related emergency room visits in 2021, according to Dorchester County health data.
Youth drug use in Dorchester County saw a 10% rise in 2020, affecting communities like Saint George, SC.
In Dorchester County, which includes Saint George, SC, 2020 data indicated methamphetamine was the most commonly abused drug.
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
Many employers in Saint George, SC, enforce strict drug testing policies to ensure a safe and productive workplace. Local companies often partner with the South Carolina Department of Health and Environmental Control to conduct random drug testing, emphasizing the importance of maintaining a drug-free environment.
Policies typically include pre-employment screenings and may also feature random or scheduled testing during employment. These initiatives aim to deter drug use among employees, offering support programs for those who test positive in collaboration with organizations like SC Department of Alcohol and Other Drug Abuse Services.
Additionally, many private employers in Saint George, SC, seek guidance from federal resources such as the U.S. Department of Labor to align their drug testing policies with national standards and support safe workplace practices.
In an effort to address drug problems in Saint George, SC, the local government, along with South Carolina Department of Health and Human Services, has increased funding for substance abuse programs. They focus on community outreach and rehabilitation services aimed at reducing drug misuse.
The federal government also supports initiatives through the Substance Abuse and Mental Health Services Administration (SAMHSA), providing Saint George, SC with resources for education and prevention campaigns. These programs aim to raise awareness and provide support to individuals and families impacted by substance abuse.
Saint George, SC, has witnessed several significant drug busts in recent years, as local law enforcement intensifies efforts to combat drug crimes. One notable event occurred in 2021, when Dorchester County deputies conducted a major operation leading to the arrest of a dozen individuals involved in drug trafficking.
Another significant incident took place in late 2022, during which police seized a large stash of illegal narcotics destined for distribution throughout Dorchester County, including key areas such as Saint George. These operations reflect the ongoing battle against drug distribution in the region.
Community initiatives and partnerships with the Drug Enforcement Administration (DEA) have been crucial in these efforts, leading to coordinated operations that have significantly disrupted the local drug trade network.
Accredited Drug Testing offers fast, reliable employment screening services in Saint George, SC. Trusted by employers nationwide for accurate results and exceptional service.
South Carolina DOT/Non DOT Physicals
South Carolina Department of Alcohol and Other Drug Abuse Services
Crossroads Treatment Centers
Alston Wilkes Society
The Journey Center
Magnolia Medical Group
Charleston Recovery Center
LRADAC
South Carolina Department of Health and Environmental Control
Alcoholics Anonymous South Carolina
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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