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At our 33 testing facilities around Speed, NC, Accredited Drug Testing delivers extensive drug and alcohol testing solutions. We cater to DOT and non-DOT requirements with urine and breath alcohol tests, EtG alcohol assessments, and hair drug evaluations for personal, workforce, and legal purposes. Rapid testing and SAMSA certified lab analyses are offered, with same-day services accessible at most sites conveniently close to your location. We also provide Occupational Health Testing, Clinical Testing, and Background Checks.
Dial (800) 221-4291 or register via our website. Pick your required test and a convenient location—ensuring it's available for you, your staff, or another party. Scheduling is a breeze: contact our team or book online anytime. Our seamless and accessible system ensures you can organize drug tests close to Speed 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 Speed 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.
Speed, located in Edgecombe County, NC, had a drug overdose death rate of 27.5 per 100,000 residents in 2021.
In 2022, 15% of high school students in Edgecombe County reported using illicit drugs, with Speed contributing significantly to these figures.
Data from 2021 shows that Speed accounted for 20% of all drug-related arrests in Edgecombe County.
Edgecombe County hospitals reported a 12% increase in emergency admissions due to drug overdoses in 2022, with Speed residents forming a considerable percentage.
In 2023, Speed, NC experienced a 32% rise in opioid-related incidents according to Edgecombe County health department data.
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 Speed, NC are committed to maintaining a drug-free workplace, implementing rigorous drug testing policies to ensure safety and productivity. This includes pre-employment screenings and random drug tests, in accordance with the U.S. Department of Labor guidelines on maintaining drug-free work environments.
Several major employers in Speed collaborate with local health organizations to offer support and counseling for employees struggling with substance abuse. Such efforts align with state regulations and policies provided by the North Carolina Department of Labor.
The government of Speed, NC, along with support from Edgecombe County, has been actively working to address the drug issues plaguing the community. Programs focused on prevention, treatment, and recovery have been implemented, thanks to funding from the North Carolina Department of Health and Human Services.
Further efforts include community education programs and partnerships with local law enforcement as part of a comprehensive plan to curb drug abuse. Funding from agencies like the Substance Abuse and Mental Health Services Administration facilitates these initiatives, ensuring resources are available for those in need.
Recently, law enforcement agencies in Speed, NC successfully executed a major drug bust, dismantling a large distribution network within Edgecombe County. This operation resulted in multiple arrests and confiscation of significant quantities of narcotics.
Community events in Speed are increasingly focused on raising awareness about drug abuse. Local organizations hold forums to discuss the impact of drugs on families and gather support for initiatives aimed at reducing substance use.
Efforts to involve youth in drug prevention have also grown, with local schools in Speed hosting educational programs and campaigns against drug use as part of a broader community outreach.
Accredited Drug Testing offers fast, reliable employment screening services in Speed, NC. Trusted by employers nationwide for accurate results and exceptional service.
North Carolina DOT/Non DOT Physicals
NC Department of Health and Human Services
Substance Abuse and Mental Health Services Administration
North Carolina Health News
NIDA
CDC Drug Overdose Maps
DEA Drug Information
National Institute on Alcohol Abuse and Alcoholism
National Crime Prevention Council
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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