superior industrial supply co. blue logo
0

Blog Layout

Meth Labs

October 2019
The asylum seekers interviewed at the bridge, requested anonymity, but otherwise spoke freely about current conditions in their home town. A small group from Ciudad Hidalgo, Michoacan explained that meth labs have popped up back home, drug abuse has skyrocketed and gangsters extort residents for payments of up to $2,000. Residents are fearful their children will be forced into the ranks of the drug gangs.


Meth Labs On The Increase Again

Instances of meth labs and methamphetamine trafficking and abuse in the United States are on the increase and it appears that opioid deaths are the trigger. As a result, this drug is having a devastating impact again on communities across the nation.

Clandestine production, Meth Labs, accounts for nearly all of the methamphetamine trafficked and abused in the United States. Domestic methamphetamine production, trafficking, and abuse are concentrated in the western, southwestern, and Midwestern United States. Methamphetamine is also increasingly available in portions of the South and the eastern United States, especially Georgia and Florida. Clandestine laboratories in California and Mexico are the primary sources of supply for methamphetamine available in the United States.


Meth Lab Injuries

Injuries and deaths due to accidents or explosions in illegal methamphetamine labs are on the rise in the United States, a new study shows. Many of the injured were law enforcement and other First Responders, as well as children who lived in the home.

Meth labs are being discovered in remote areas of some of our national forests. These labs are an environmental hazard, the byproducts of meth labs contaminate the ground, lakes, and streams with harmful and highly explosive chemical compounds. Abandoned meth labs are basically time bombs, waiting for the single spark that can ignite the contents of the lab or a tourist visiting the park.


One-Pot Meth Labs

Meth labs of the past (referred to as garage labs) required hundreds or thousands of cold tablets, a large quantity of fuel, other household chemicals, glassware and other products and a room large enough to set up the lab. Making meth using the “one pot” method, is accomplished by pouring all the ingredients into a plastic soda bottle, or other container. The ingredients are then mixed by shaking (shake and bake) the container and regulating the pressure created by the chemical reaction of the cold tablets and household chemicals. The quantity of meth is small, usually enough for one or two doses, with quality varying.


Mexican Meth Labs

Mexican drug trafficking organizations have become the primary manufacturers and distributors of methamphetamine to cities throughout the United States, including in Hawaii. Domestic clandestine laboratory operators also produce and distribute meth but usually on a smaller scale. The methods used depend on the availability of precursor chemicals.


Currently, this domestic clandestinely produced meth is mainly made with diverted products that contain pseudoephedrine. Mexican methamphetamine is made with differ­ent precursor chemicals.

Source: DEA


Methamphetamine is clandestinely manufactured in Meth Labs using the ephedrine or pseudoephedrine reduction method. In this process, over-the-counter cold and allergy tablets containing ephedrine or pseudoephedrine are placed in a solution of water, alcohol, or another solvent for several hours until the ephedrine or pseudoephedrine separates from the tablet. Then, using common household products and equipment listed on the following page and a recipe learned from friends or taken off the Internet, the ephedrine or pseudoephedrine is converted into high-quality Methamphetamine in makeshift, illegal labs by untrained individuals.

The state of Oregon requires a prescription to purchase certain over-the-counter medications that can be used to make methamphetamine. Other states are considering similar laws.


Household products contain most of the necessary chemicals to complete the manufacturing process. Certain brands of drain cleaner, for instance, have a high concentration of sulfuric acid. When mixed with table or rock salt, hydrogen chloride gas is produced for use in the final stage of methamphetamine production.


The hydrogen chloride gas procedure as well as other procedures are extremely dangerous and can cause death or serious injury not only to the individuals making the methamphetamine but to others who may be living in an adjoining house or apartment.

The chemicals used to make meth are toxic, and the lab operators routinely dump waste into streams, rivers, fields, and sewage systems. The chemical vapors produced during cooking permeate the walls and carpets of houses and buildings, making them uninhabitable. Cleaning up these sites requires specialized training and costs an average of $2,000-$4,000 per site in funds that come out of the already-strained budgets of state and local police.

Common Chemicals Used to Make Methamphetamine:

Alcohol (Isopropyl or rubbing alcohol)
Toluene (brake cleaner)
Ether (engine starter)
Sulfuric Acid (drain cleaner)
Red Phosphorus (matches/road flares)
Salt (table/rock)
Iodine (teat dip or flakes/crystal)
Lithium (batteries)
Trichloroethane (gun scrubber)
MSM (cutting agent)
Sodium Metal
Methanol/Alcohol (gasoline additives)
Muriatic Acid
Anhydrous Ammonia (farm fertilizer)
Sodium Hydroxide (lye)
Pseudoephedrine (cold tablets)
Ephedrine (cold tablets)
Acetone, Cat Litter


Typical Equipment Used to Make Methamphetamine:

Pyrex or Corning dishes (glass)
Jugs/bottles
Paper towels
Coffee filters
Thermometer
Cheesecloth
Funnels
Blenders
Rubber tubing/gloves
Pails/buckets
Gas Cans
Tape/clamps
Internet documents/notes
“How to Make Methamphetamine” books
Aluminum foil
Propane cylinders (20-lb)
Hotplates
Plastic storage containers/ice chests
Measuring cups
Towels/bed sheets
Laboratory beakers/glassware


By Bob Hansen January 29, 2022
Zyprexa (Olanzapine) is used to treat the symptoms of psychotic conditions such as schizophrenia and bipolar disorder. More information/images in the Prescription Drug Brochure. When you receive Zyprexa extended-release injection, the medication is usually released slowly into your blood over a period of time. However, when you receive olanzapine extended-release injection, there is a small chance that olanzapine may be released into your blood too quickly. If this happens, you may experience a serious problem called Post-injection Delirium Sedation Syndrome (PDSS). If you develop PDSS, you may experience dizziness, confusion, difficulty thinking clearly, anxiety, irritability, aggressive behavior, weakness, slurred speech, difficulty walking, muscle stiffness or shaking, seizures, drowsiness, and coma (loss of consciousness for a period of time). You are most likely to experience these symptoms during the first 3 hours after you receive the medication. You will receive Zyprexa extended-release injection in a hospital, clinic, or another medical facility where you can receive emergency medical treatment if it is needed. You will need to remain in the facility for at least 3 hours after you receive the medication. While you are in the clinic, the medical staff will watch you closely for signs of PDSS. When you are ready to leave the facility, you will need a responsible person to be with you, and you should not drive a car or operate machinery for the rest of the day. Get emergency medical help right away if you experience any symptoms of PDSS after you leave the facility. A program has been set up to help people receive Zyprexa extended-release injection safely. You will need to register and agree to the rules of this program before you receive olanzapine extended-release injection. Your doctor, the pharmacy that dispenses your medication, and the medical facility where you receive your medication will also need to register. Ask your doctor if you have any questions about this program. For people being treated with olanzapine extended-release injection or Zyprexa injection: Studies have shown that older adults with dementia (a brain disorder that affects the ability to remember, think clearly, communicate, and perform daily activities and that may cause changes in mood and personality) who take antipsychotics (medications for mental illness) such as olanzapine have an increased chance of death during treatment. Older adults with dementia may also have a greater chance of having a stroke or mini-stroke during treatment. Olanzapine injection and olanzapine extended-release injection are not approved by the Food and Drug Administration (FDA) for the treatment of behavior disorders in older adults with dementia. Talk to the doctor who prescribed this medication if you, a family member, or someone you care for has dementia and is being treated with olanzapine injection or olanzapine extended-release injection. For more information visit the FDA website: http://www.fda.gov/Drugs Your doctor or pharmacist will give you the manufacturer’s patient information sheet (Medication Guide) when you begin treatment with olanzapine extended-release injection and each time you receive an injection. Read the information carefully and ask your doctor or pharmacist if you have any questions. You can also visit the Food and Drug Administration (FDA) website (http://www.fda.gov/Drugs/DrugSafety/ucm085729.htm) or the manufacturer’s website to obtain the Medication Guide. extended-release injection, the medication is usually released slowly into your blood over a period of time. However, when you receive olanzapine extended-release injection, there is a small chance that olanzapine may be released into your blood too quickly. If this happens, you may experience a serious problem called Post-injection Delirium Sedation Syndrome (PDSS). If you develop PDSS, you may experience dizziness, confusion, difficulty thinking clearly, anxiety, irritability, aggressive behavior, weakness, slurred speech, difficulty walking, muscle stiffness or shaking, seizures, drowsiness, and coma (loss of consciousness for a period of time). You are most likely to experience these symptoms during the first 3 hours after you receive the medication. You will receive olanzapine extended-release injection in a hospital, clinic, or another medical facility where you can receive emergency medical treatment if it is needed. You will need to remain in the facility for at least 3 hours after you receive the medication. While you are in the clinic, the medical staff will watch you closely for signs of PDSS. When you are ready to leave the facility, you will need a responsible person to be with you, and you should not drive a car or operate machinery for the rest of the day. Get emergency medical help right away if you experience any symptoms of PDSS after you leave the facility. A program has been set up to help people receive olanzapine extended-release injection safely. You will need to register and agree to the rules of this program before you receive olanzapine extended-release injection. Your doctor, the pharmacy that dispenses your medication, and the medical facility where you receive your medication will also need to register. Ask your doctor if you have any questions about this program. For people being treated with olanzapine extended-release injection or olanzapine injection: Studies have shown that older adults with dementia (a brain disorder that affects the ability to remember, think clearly, communicate, and perform daily activities and that may cause changes in mood and personality) who take antipsychotics (medications for mental illness) such as olanzapine have an increased chance of death during treatment. Older adults with dementia may also have a greater chance of having a stroke or mini-stroke during treatment. Olanzapine injection and olanzapine extended-release injection are not approved by the Food and Drug Administration (FDA) for the treatment of behavior disorders in older adults with dementia. Talk to the doctor who prescribed this medication if you, a family member, or someone you care for has dementia and is being treated with olanzapine injection or olanzapine extended-release injection. For more information visit the FDA website: http://www.fda.gov/Drugs  Your doctor or pharmacist will give you the manufacturer’s patient information sheet (Medication Guide) when you begin treatment with olanzapine extended-release injection and each time you receive an injection. Read the information carefully and ask your doctor or pharmacist if you have any questions. You can also visit the Food and Drug Administration (FDA) website (http://www.fda.gov/Drugs/DrugSafety/ucm085729.htm) or the manufacturer’s website to obtain the Medication Guide.
By Bob Hansen January 29, 2022
Zoloft (Sertraline) is included in the class of drugs called selective serotonin reuptake inhibitors (SSRIs). This class of drugs is used to treat depression, anxiety, and other mood disorders.
By Bob Hansen January 29, 2022
Zanaflex (Tizanidine) is a short-acting muscle relaxer. Tizanidine is used to relieve the spasms and increased muscle tone caused by multiple sclerosis (MS, a disease in which the nerves do not function properly and patients may experience weakness, numbness, loss of muscle coordination and problems with vision, speech, and bladder control), stroke, or brain or spinal injury. Tizanidine is in a class of medications called skeletal muscle relaxants. It works by slowing action in the brain and nervous system to allow the muscles to relax. Tizanidine comes as a tablet and a capsule to take by mouth. It is usually taken consistently either always with or always without food two or three times a day. Follow the directions on your prescription label carefully, and ask your doctor or pharmacist to explain any part you do not understand. Take tizanidine exactly as directed. Do not take more or less of it or take it more often than prescribed by your doctor. Tizanidine capsules may be opened and sprinkled on soft foods such as applesauce. Talk to your doctor before opening the capsules because the effects of the medication, when used in this manner, may be different than when swallowing the capsule whole. The medication in the capsule is absorbed differently by the body than the medication in the tablet, so one product cannot be substituted for the other. Each time you have your prescription filled, look at the tablets or capsules in the bottle and make sure that you have received the right product. If you think you received the wrong medication, talk to your doctor or pharmacist right away. Your doctor will probably start you on a low dose of tizanidine and gradually increase your dose, depending on your response to this medication.  Do not stop taking tizanidine without talking to your doctor. If you suddenly stop taking tizanidine, your heart may beat faster and you may have increased blood pressure or tightness in your muscles. Your doctor will probably decrease your dose gradually.
More Posts
Share by: