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Accredited Drug Testing delivers extensive drug and alcohol testing options through our 32 centers located in the Kennedale, Texas region. Catering to DOT and non-DOT requirements, our services include urine drug testing, breath alcohol analysis, EtG alcohol screenings, and hair follicle drug assessments for personal, corporate, and judicial purposes. In Kennedale, TX, we offer rapid result services and SAMSA verification laboratory diagnostics with availability for same-day appointments. Numerous testing sites are situated conveniently close to residential and business areas. Additional offerings involve Occupational Health Services, Clinical Assessments, and Background Evaluation.
Dial (800) 221-4291 or complete your registration online. Pick your desired test and select the closest center—testing can be set up for yourself, staff, or another person. It's quick and straightforward to schedule, either by contacting our scheduling team or by using our 24/7 online platform. Our smooth and intuitive system makes it simple to organize drug evaluations near Kennedale.
* 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 Kennedale 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 Kennedale, Tarrant County, opioid-related overdoses have increased by 15% over the past five years.
Kennedale, Tarrant County reported 125 drug-related arrests in 2022, marking a 10% rise from 2021.
In 2022, Kennedale High School, Tarrant County, reported 30 incidents of drug-related infractions.
Tarrant County, including Kennedale, saw a 7% increase in methamphetamine usage rates in 2022.
Kennedale, Tarrant County, witnessed a 25% increase in hospital admissions due to drug abuse in 2022.
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
In Kennedale, TX, employers are proactive in maintaining a drug-free environment. Many companies follow the guidelines provided by the U.S. Department of Labor, which recommends regular drug testing and educational programs to ensure safety and productivity.
The Texas Workforce Commission supports employers with resources to develop policies addressing substance use; links such as Texas Workforce Commission provide insights and assistance.
The City of Kennedale in Tarrant County has been actively working to combat drug issues through various initiatives. Partnerships with CDC and SAMHSA have helped implement educational programs for youth.
Moreover, the city collaborates with Tarrant County authorities to increase funding for local rehab centers and works with state agencies to enhance community outreach programs, focusing on prevention and treatment.
In recent years, Kennedale, TX, has witnessed an uptick in local drug busts, reflecting a larger trend seen across Tarrant County. Police efforts have intensified, aiming to dismantle networks that contribute to the proliferation of illicit substances. Coordinated operations have led to multiple seizures and arrests, helping to curb the drug trade and promote safety within the community.
Joint efforts between Kennedale law enforcement and neighboring jurisdictions have proven effective in tackling drug-related events. These collaborations often involve information sharing and strategic planning to address incidents efficiently. Recent operations have targeted both small-scale dealers and larger distribution rings, showcasing a proactive stance against drug activity in the area.
Community involvement in Kennedale has also played a crucial role in addressing the local drug issue. Residents are increasingly vigilant, reporting suspicious activities to authorities, which in turn aids in prompt interventions. Public awareness campaigns are continuously being rolled out, focusing on education about the dangers of drug misuse and the importance of community policing.
Accredited Drug Testing offers fast, reliable employment screening services in Kennedale, TX. Trusted by employers nationwide for accurate results and exceptional service.
Texas State of Mind
Texas Department of State Health Services
Sober Austin
North Central Texas Trauma Regional Advisory Council
Texas Overdose Awakening
Partners in Recovery
Recovery Resource Council
Touchstone Ranch Recovery Center
Substance Abuse Rehab Texas
Oceans Healthcare
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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