How Long Do Muscle Relaxers Stay In Your System

A muscle relaxant is a drug that affects skeletal muscle function and decreases the muscle tone. It may be used to alleviate symptoms such as muscle spasms, pain, and hyperreflexia. The term “muscle relaxant” is not a class of drugs but used to refer to two major therapeutic groups: neuromuscular blockers and spasmolytics.

Muscle relaxers are used in addition to rest, physical therapy, and other measures to relieve discomfort. They are typically prescribed for short-term use to treat acute, painful musculoskeletal conditions. Muscle relaxers are occasionally prescribed for chronic pain (pain lasting longer than 3 months).

 

How do muscle relaxants work?

Muscle relaxants work by causing the muscles to become less tense or stiff, which in turn reduces pain and discomfort. They do this in different ways. Baclofen, diazepam, methocarbamol and tizanidine act on the central nervous system (brain and spinal cord). Dantrolene works directly on the muscle. Cannabis extract works on the brain and spinal cord as well as the muscles. Because dantrolene only works on the muscles, it is thought to have fewer side-effects compared with other muscle relaxants. For this reason, dantrolene is often the first muscle relaxant to be prescribed for people with long-term muscle spasms.

 

How Long Do Muscle Relaxers Stay In Your System

The specific drug taken, drug taking habits, amount consumed, age, weight, and gender all influence the length of time a drug stays in your system. Other factors include how the drug was taken, whether other drugs were used, ethnicity, and medical conditions such as kidney problems can determine how long muscle relaxers stay in the body.

Since muscle relaxers are not a class of drugs they do not all have the same chemical structure, work the same way or stay in your body at the same rate. In this article we have listed the common muscle relaxants and how long they last in your body:

 

Baclofen. Sold under the brand name Lioresal among others, is a medication used to treat muscle spasticity such as from a spinal cord injury or multiple sclerosis. It may also be used for hiccups and muscle spasms near the end of life. It is taken by mouth or by delivery into the spinal canal. Baclofen is rapidly absorbed, although absorption may be reduced with higher dosages.

There is a wide variation in the way individuals respond to baclofen, with some people reporting a reduction in symptoms of muscle spasm within a few hours, whereas for some others it may take several weeks. The drug is predominantly excreted unchanged by the kidneys. The half-life of baclofen is roughly 2–4 hours; it therefore needs to be administered frequently throughout the day to control spasticity appropriately.

 

Benzodiazepines. In addition to treating anxiety, alcohol withdrawal, and seizure disorders, such as epilepsy, benzodiazepines can also treat muscle spasms and skeletal pain. Benzodiazepines, such as diazepam (Valium), lorazepam (Ativan), and temazepam (Restoril), are typically only intended for short-term use. Benzodiazepines are well known for their strong muscle-relaxing properties and can be useful in the treatment of muscle spasms, although tolerance often develops to their muscle relaxant effects. Benzodiazepines can stay in urine 3 to 6 weeks, hair up to 90 days, and blood 2-3 days. ALSO READ: How Long Does Blue B707 Pill Last?

 

Carisoprodol (Soma). Carisoprodol relaxes muscles and eases pain and stiffness caused by acute bone and muscle problems, often caused by an injury. It is taken by mouth in tablet form and is also available in combination with aspirin or aspirin and codeine. Carisoprodol can be habit-forming, particularly if used in conjunction with alcohol or other drugs that have a sedative effect, including opioids (such as codeine). Carisoprodol is absorbed and begins to have effects after 30 minutes and the effects last for 4 to 6 hours. Both carisoprodol and its metabolite meprobamate are excreted in the urine and can be detected for several days after the last dose.

 

Chlorzoxazone (Lorzone). Chlorzoxazone is used for the relief of discomfort from acute, painful, musculoskeletal conditions. Chlorzoxazone is available as a tablet. Common side effects include drowsiness, dizziness, and nausea. Chlorzoxazone is not recommended for people with liver disease. Chlorzoxazone is rapidly metabolized and is excreted in the urine, primarily in a conjugated form as the glucuronide. Less than one percent of a dose of Chlorzoxazone is excreted unchanged in the urine in 24 hours.

 

Cyclobenzaprine (Amrix, Fexmid, FlexePax Kit, FusePaq Tabradol). Cyclobenzaprine popularly known by the brand Flexeril eases stiffness and pain from muscle cramps, also called muscle spasms. It is available as a tablet and extended-release capsule. Cyclobenzaprine itself is not intended for long-term use (more than 2 to 3 weeks). Levels of Cyclobenzaprine in your system peak approximately three to four hours after taking the medication, after which time the effects begin to diminish. Most people feel the effects of Cyclobenzaprine for about four to six hours.

However, just because you stop feeling the effects of Cyclobenzaprine does not mean that the medication has left your system. Cyclobenzaprine is detected in a urine sample for anywhere from three to eight days after taking your last dose, and it appears in a blood test and drug test for up to 3.75 days after it is last ingested. Cyclobenzaprine stays in your saliva for 36 hours after use, and it is unknown how long it stays in your. ALSO READ: How To Flush Flexeril Out Of Your System

 

Dantrolene (Dantrium). Dantrolene helps control chronic spasticity related to spinal injuries. It is also used for conditions such as stroke, multiple sclerosis, and cerebral palsy. Dantrolene is taken as a capsule or intravenous powder for injection. Drowsiness and sensitivity to light are common side effects. It can cause severe liver problems, and should not be taken by people with active liver disease. The duration and intensity of skeletal muscle relaxation is related to the dosage and blood levels. The mean biologic half-life of Dantrolene sodium in adults is 8.7 hours after a 100-mg dose.

 

Metaxalone (Skelaxin, Metaxall, and Metaxall CP, Lorvatus PharmaPak). Metaxalone targets pain and muscle spasms from sprains, strains, and muscle injuries. It is available as a tablet or injection. Absorption. Peak plasma concentrations of metaxalone occur approximately 3 hours after a 400 mg oral dose under fasted conditions. Thereafter, metaxalone concentrations decline log-linearly with a terminal half-life of 9.0 ± 4.8 hours.

 

Methocarbamol (Robaxin, Robaxin-750). Methocarbamol eases acute muscle and bone pain. It can be taken as a tablet or by injection. Methocarbamol is generally not recommended to people with renal disease or failure, or a history of allergic reaction to the medication. At the time of ingestion, Methocarbamol can last in the urine of an individual for a total of four hours. This can vary from person to person depending on their health or age. ALSO READ: Does Methocarbamol Show Up As On A Drug Test

 

Orphenadrine. Orphenadrine is a medication used to relieve pain and stiffness caused by muscle injuries. It is available as an extended-release tablet. Common side effects include dry mouth, lightheadedness, difficult urination, heartburn, nausea and vomiting. It is generally not recommended to people with previous sensitivities to the ingredients, myasthenia gravis, those with glaucoma or certain types of ulcers. Orphenadrine is readily absorbed from the gastrointestinal tract and is almost completely metabolized to at least eight metabolites. Orphenadrine and its metabolites are excreted from the body in the urine, with a half-life of 14 hours.

 

Tizanidine (Comfort Pac with Tizanidine, Zanaflex). Tizanidine is used to treat muscle spasms caused by spinal cord injuries and other conditions such as multiple sclerosis. Tizanidine is available in tablet and capsule form and absorbs differently depending on whether it is taken on an empty stomach or with food. Tizanidine has a short “half-life” of only about 150 minutes, which means that the body clears the drug within a few hours. Common side effects include dry mouth, dizziness, constipation and tiredness. It should not be used by people taking fluvoxamine or ciprofloxacin or those who have liver disease.

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