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Accredited Drug Testing provides an extensive range of drug and alcohol exams at 24 locations in the Farmingdale, Maine area. Our services include DOT and non-DOT urine screenings, breath alcohol tests, EtG alcohol assessments, and hair drug analyses, catering to personal, professional, and legal requirements. For those in Farmingdale, ME, we promise rapid testing outcomes and SAMSA lab certification, with same-day services at most centers, conveniently located near you. We also offer Occupational Health Testing, Clinical Testing, and Background Checks.
To schedule, contact us at (800) 221-4291 or register online. Choose the desired test and a suitable center—services are available for individuals, employees, or third parties. With our Fast and Easy scheduling system, you can effortlessly arrange a test online or through our department, available 24/7. Our efficient process simplifies setting up drug testing locally near Farmingdale.
* 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 Farmingdale 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.
Farmingdale, ME in Kennebec County has seen a 7% rise in opioid-related arrests over the past year.
Drug overdoses in Farmingdale, ME accounted for 12% of all emergency calls in 2022.
Teen drug use in Farmingdale, ME is reported to be slightly above the state average at 19%.
Kennebec County recorded 18 drug-related deaths in 2022, with several cases stemming from Farmingdale.
Methamphetamine use in Farmingdale, ME has increased by 10% in the past two years.
Farmingdale, ME saw a 15% increase in drug-related crime between 2021 and 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 Farmingdale, ME, numerous employers have established stringent drug testing policies to ensure a safe and productive work environment. Local businesses, particularly those in construction and healthcare, often require pre-employment drug screenings as well as random checks to deter substance abuse.
These policies align with regulations set by the Maine Department of Labor, which provides guidelines on drug testing in the workplace. Employers are keen on maintaining compliance while fostering a supportive environment for employees seeking help for addictions.
The government of Farmingdale, ME, alongside Kennebec County, has made significant efforts to combat drug abuse. Partnering with the Maine Office of Substance Abuse, new community programs have been launched to offer education and support to those struggling with addiction.
Moreover, the state government has provided funds to improve law enforcement training in addressing drug addiction issues. Collaboration with agencies such as the Know Your Options program aims at offering comprehensive resources to residents. These initiatives are part of a broader strategy to reduce drug-related crime and help affected individuals recover.
Recent months have seen several drug busts in Farmingdale, ME, as local law enforcement continues to crack down on illegal drug activities. In a coordinated effort with Kennebec County officials, a large operation was conducted in early 2023, resulting in multiple arrests and the seizure of significant quantities of narcotics.
Such events highlight the ongoing challenges faced by the community and the proactive stance taken by authorities. Public awareness campaigns and coordinated actions have proven effective in identifying and dismantling drug networks that pose a threat to public safety in Farmingdale.
Accredited Drug Testing offers fast, reliable employment screening services in Farmingdale, ME. Trusted by employers nationwide for accurate results and exceptional service.
Maine Office of Substance Abuse
Substance Abuse and Mental Health Services Administration
Know Your Options
Maine Drug Enforcement Agency
Maine's Healthy Partnerships
Sober Nation - Maine
The Good Drugs Guide - Maine
Rehab Center.net - Maine
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Time was running out before my Cdl got downgraded because of a violation I had on clearinghouse. I couldn't find an employer to send me for my return to duty test, but these guys had my test scheduled and done in the same day! They saved my cdl. Thank you again!
Michael Williams - 12/2/2024
I always have a good experience setting up company driver drug screens through ADT. I'm really happy I found them while searching online, they have made my job much easier.
Exodus Heath - 2/13/2025
I use their service for new hire and DOT employee's. Spoke with Taisha Walker this morning, and she was very helpful. She made the process smooth and seamless.
Christina Galdos - 3/9/2025