Deep Sleep Pills

Deep Sleep Pills Rating: 6,8/10 3841 reviews

Deep sleep re-establishes natural sleep patterns by retraining the brain's sleep center and reduces the amount of time it takes to fall asleep. A must when traveling to new locations or different time zones; useful when working swing-shift schedules. More people experience restful sleep with deep sleep than with any other herbal. Dec 14, 2018  My deep sleep most nights is less than 20 minutes and I wake up feeling like I immediately need a nap. I take Melatonin, L-Theanine (3), Moon Drops, and an evening testosterone supplement.

Sleep disorders can be divided into those producing insomnia, those causing daytime sleepiness, and those disrupting sleep. Transient insomnia is extremely common, afflicting up to 80% of the population. Chronic insomnia affects 15% of the population. Benzodiazepines are frequently used to treat insomnia; however, there may be a withdrawal syndrome with rapid eye movement (REM) rebound.

Two newer benzodiazepine-like agents, zolpidem and zaleplon, have fewer side effects, yet good efficacy. Other agents for insomnia include sedating antidepressants and over-the-counter sleep products (sedating antihistamines). Nonpharmacologic behavioral methods may also have therapeutic benefit. An understanding of the electrophysiologic and neurochemical correlates of the stages of sleep is useful in defining and understanding sleep disorders. Excessive daytime sleepiness is often associated with obstructive sleep apnea or depression. Cops n robbers minecraft server. Medications, including amphetamines, may be used to induce daytime alertness.

Parasomnias include disorders of arousal and of REM sleep. Chronic medical illnesses can become symptomatic during specific sleep stages. Many medications affect sleep stages and can thus cause sleep disorders or exacerbate the effect of chronic illnesses on sleep. Conversely, medications may be used therapeutically for specific sleep disorders. For example, restless legs syndrome and periodic limb movement disorder may be treated with dopamine agonists.

An understanding of the disorders of sleep and the effects of medications is required for the appropriate use of medications affecting sleep. Each of us will spend a third of our lives asleep. Sleep is a complex and pervasive cognitive state affected by medications in many different ways.

The field of sleep disorders medicine has become increasingly complex with more than 90 disorders of sleep described, each with clear diagnostic criteria. An even larger group of diseases produces mental or physical discomfort affecting sleep. Sleep disorders can generally be divided into 3 large groups: (1) those producing insomnia (complaints of difficulty falling asleep, staying asleep, or nonrestorative sleep), (2) those with a primary complaint of daytime sleepiness, and (3) those associated with disruptive behaviors during sleep—the disorders of arousal. There is a full range of medications used to treat these disorders, each with particular benefits as well as potential for harm. Sedatives and HypnoticsInsomnia is an extremely common complaint.

Transient insomnia (. Diagnoses Resulting in Chronic Insomnia aHistorically, sedative/hypnotics have been some of the most commonly prescribed drugs. Chloral hydrate was the original “Mickey Finn” slipped into the drinks of unsuspecting marks for the purposes of criminal activity. Unfortunately, the median lethal dose (LD 50) for chloral hydrate is quite close to the therapeutic dose, and murders rather than robberies were often the result. In the years leading up to the 1960s, barbiturates were commonly utilized for their sedative effects. Unfortunately, these medications can be drugs of abuse and have a significant danger of overdose.

Marilyn Monroe, Elvis Presley, and Jim Morrison, among others, were celebrities who died during this era from overdoses of sleeping pills. These medications and similar barbiturate-like medications (methaqualone, glutethimide, ethchlorovynol, methyprylon) can still be prescribed, but should be used sparingly because of their potential for abuse and overdose.In the 1970s benzodiazepines became available for the treatment of insomnia. These drugs act at γ-aminobutyric acid (GABA) neuroreceptors and have far less overdose danger and abuse potential than previous medications used for sleep. The many drugs in this class are best viewed therapeutically based on their pharmacodynamics. Rapid onset of action is characteristic of flurazepam and triazolam, indicating that both of these agents have excellent sleep-inducing effects. Flurazepam, like diazepam and clorazepate, has active breakdown products.

This characteristic results in an extraordinarily long active half-life, which can approach 11 days. This prolonged effect in the elderly has been associated with increased auto accidents and falls with hip fractures. Withdrawal from these long-acting agents can be difficult, causing an initial syndrome of insomnia followed by persistent anxiety that may extend beyond the half-life of the agent. Benzodiazepines are rapid eye movement (REM) sleep–suppressant medications, and withdrawal often results in episodes of increased REM sleep (REM sleep rebound). REM sleep is known to have a role in learning and memory consolidation. For short-acting agents such as triazolam, this rebound occurs during the same night in which the medication was taken and has been associated with daytime memory impairment, particularly at higher dosages. Temazepam and estazolam have half-lives compatible with an 8-hour night of sleep.

Temazepam, because of its slower onset of action, is less efficacious as a sleep-inducing agent than other drugs used as hypnotics in this class. All benzodiazepines can result in respiratory depression in patients with pulmonary disease and may lose sleep-inducing efficacy with prolonged use.The newer hypnotics zolpidem and zaleplon are benzodiazepine-like agents, exerting effects at the same GABA receptors. Withdrawal from benzodiazepines is not blocked by these agents. Both have excellent efficacy with minimal side effects. Abuse potential for these agents is minimal, although any agent used to induce sleep can result in a dependence on that agent to induce sleep. Idiosyncratic reactions of persistent daytime somnolence and/or memory loss have been reported in some patients. Tachyphylaxis is unusual, and thus they can be used on a long-term basis.

Sleep is altered minimally, and REM rebound is not associated with these agents. Zolpidem has a 6- to 8-hour half-life and zaleplon is shorter acting (3–4 hours). Clinical comparison of these agents suggests that zolpidem may have greater sleep-inducing efficacy and zaleplon, fewer side effects.In the last 30 years, although the drugs for treatment of insomnia have become safer, the number of sedatives and hypnotics prescribed in the United States has declined. This decrease most likely reflects the public's and the medical community's increasing understanding of the side effects and limitations of the available hypnotic drugs. Nonpharmacologic behavioral methods, such as sleep hygiene, hypnosis, relaxation training, sleep restriction, and cognitive therapies, have shown therapeutic benefit in the treatment of insomnia.The physician treating insomnia should make the appropriate diagnosis before initiating therapy. Insomnia is commonly a symptom of nocturnal discomfort, whether psychological, physical, or environmental. Medications, in general, can be safely utilized on a short-term basis for the treatment of transient insomnia.

Chronic hypnotic medication use has been associated with the development of mood disorders (depression) and hypnotic-dependent disorders of sleep. Therefore, the underlying reasons and diseases resulting in chronic insomnia should be addressed. Approximately 10% of the cases of chronic insomnia are due to anxiety or panic disorder. For patients in this category and those with idiopathic insomnia (persistent lifelong insomnia without other sleep-associated diagnoses), chronic hypnotic use can be justified and is indicated. Other Sedating AgentsEthanol is probably the most widely used hypnotic medication.

In patients with chronic insomnia, 22% report using ethanol as a hypnotic. Unfortunately, chronic use to induce sleep can result in tolerance, dependence, and diminished sleep efficiency and quality. When ethanol is used in excess with other sedative/hypnotic agents, overdose can be fatal.Over-the-counter sleeping pills contain sedating antihistamines, usually diphenhydramine. These agents are varyingly effective, but may result in daytime sleepiness, cognitive impairment, and anticholinergic effects that persist into the day after use, affecting driving performance. These agents are not recommended for use in the elderly.

Seizure thresholds can be lowered by their use in epileptic patients. The side effect profiles of the newer sedatives and hypnotics are generally more benign that those of the sedating antihistamines. AnidepressantsSedating antidepressants are often used to treat insomnia. A significant percentage of individuals with chronic insomnia and/or daytime sleepiness also have depressive symptoms. Chronic insomnia itself can lead to depression.

Depression associated with insomnia is likely a different diagnostic entity than depression without insomnia, and treatment of the former with nonsedating antidepressants may produce no improvement in sleep even when the underlying depression resolves. Use of antidepressants is limited by side effects (anticholinergic effects, daytime hangover, etc.) and danger with overdose (particularly the tricyclics).

Sedating antidepressants include the tricyclics (amitriptyline, imipramine, nortriptyline, etc.), trazodone, and the newer agents mirtazapine and nefazodone. The selective serotonin reuptake inhibitors (SSRIs) have a tendency to induce insomnia; however, in some patients, paroxetine may induce mild sedation. Depression-related insomnia responds to sedating antidepressants more rapidly and with lower doses compared with other symptoms of depression. In patients with insomnia and concomitant depression, antidepressants are often used in combination with sedative/hypnotic medications. MEDICATIONS INDUCING INSOMNIAMost medications affecting central nervous system (CNS) functioning can induce insomnia in some patients. A sleep history in a patient with insomnia should include a review of all medications, including OTC products. Common culprits include medications affecting neurotransmitters, such as norepinephrine, serotonin, acetylcholine, or dopamine.

Less commonly, agents such as antibiotics, antihypertensives, oral contraceptives, and thyroid replacements can induce insomnia in susceptible individuals. Over-the-counter medications that may induce insomnia include decongestants (including nose sprays), weight loss agents, ginseng preparations, and high-dose vitamin B 1. Finally, chronic and long-term sedative/hypnotic use to induce sleep may cause tolerance to the sedative effect and can contribute to chronic insomnia. Daytime SleepinessSurprisingly, despite insomnia being such a common complaint, many patients presenting with symptoms of a sleep disorder are not complaining of insomnia. Excessive daytime sleepiness is present in 5% to 15% of the population.

Many patients with excessive daytime sleepiness, particularly those who also complain of snoring, will require overnight sleep evaluation (polysomnography) because of the potential diagnosis of obstructive sleep apnea. Obstructive sleep apnea is usually treated with continuous positive airway pressure (CPAP), a system that utilizes positive nasal pressure to maintain airway patency during sleep. Other treatment approaches for obstructive sleep apnea include ear-nose-throat surgery and dental mouthpieces.

Symptoms of a mood disorder (depression), which is also a common cause of daytime sleepiness, can be difficult to distinguish from the symptoms of obstructive sleep apnea. Chronic sleep deprivation as a basis for daytime sleepiness is particularly common in the adolescent and young adult population. Less common causes of excessive daytime sleepiness are neurologic diseases that induce sleepiness: narcolepsy and idiopathic hypersomnolence. A major concern in such sleepy patients is the potential danger to self and others while working and/or driving motor vehicles.

Altering MedicationsMedications that are used in somnolent patients to induce alertness include the amphetamines (dextroamphetamine and methylphenidate) and pemoline. Pemoline can cause hepatic toxicity in susceptible patients. The amphetamines are considered to have high abuse potential and are Schedule II prescription drugs. The newer alerting agent modafinil is pharmacologically distinct and has less potential for abuse (Schedule IV). Side effects of these drugs include personality changes, tremor, hypertension (dextroamphetamine and methylphenidate), headaches, and gastrointestinal reflux.

MEDICATION-INDUCED ALTERATIONS IN SLEEP STAGES AND SLEEP EEGSleep stages were first defined in the mid-1960s, after telemetric techniques developed for monitoring the physiologic functions of astronauts were adapted for sleep monitoring. Polysomnographic recordings using electrooculogram (EOG), electromyogram (EMG), and electroencephalogram (EEG) can be used to divide sleep into stages. In some ways, sleep staging is an artificial construct designed for analysis of sleep based on our available monitoring techniques. However, research has revealed that these sleep stages have physiologic and behavioral correlates that are clinically important. REM sleep occurs about every 90 minutes and is sometimes followed by short periods of waking. During REM sleep, low voltage, fast EEG activity is associated with rapid movements of the eyes and low EMG tone in most antigravity muscles. Non-REM (NREM) sleep is divided into stages 1 to 4.

Stage 1 sleep is the transition from drowsy wake to sleep and is characterized by slow rolling eye movements and the disappearance of the EEG alpha rhythm. Stage 2, often the stage dominating much of the night, is light sleep, defined by the presence of sleep spindles and K complexes on the EEG. Stages 3 and 4, also known as deep sleep, include large amounts of the slow (1 Hz) delta rhythm on the EEG. Sleep stages occur in cycles throughout the night.

Characteristic Electroencephalographic Patterns of Human Sleep Stages aSleep-state alteration is frequently seen with psychoactive medication use. CNS active medications often alter the occurrence, latency, and EEG characteristics of specific sleep/dream states, either with therapeutic intent or as side effects. Even some nonpharmacologic therapies, such as oxygen, CPAP, and electroconvulsive therapy, can alter REM sleep and deep sleep.Medications that produce psychoactive effects alter the EEG.

Psychoactive medication effects can vary with the alterations that the drugs produce in the EEG. Typically, psychoactive medications alter background EEG frequencies and the occurrence, frequency, and latency of the various sleep stages ( and ). In general, drug-induced EEG changes are associated with characteristic behavioral effects. This relationship has been utilized to suggest therapeutic possibilities for medications that produce characteristic EEG effects.

Sleep State–Specific Diagnoses and SymptomsParasomnias are sleep disorders that occur during arousal, partial arousal, or sleep state transition. The arousal disorders are associated with arousals from deep sleep, usually during the first deep-sleep episode of the night (typically 1:00–3:00 a.m.). Arousal disorders include sleep terrors, somnambulism (sleep walking), and confusional arousals.

These conditions are most common in children, with occurrence declining markedly after the onset of adolescence. REM sleep parasomnias include sleep paralysis, sleep-related painful erections, REM sleep–related sinus arrest, nightmare syndrome, and REM behavior disorder. REM sleep alters many physiologic processes, and therefore it is not surprising that a variety of physical illnesses become symptomatic during REM sleep. Respiratory muscle atonia associated with REM sleep can result in increased sleep apnea, particularly in patients with chronic obstructive pulmonary disease (COPD). Lower esophageal pressure, also characteristic of REM sleep, can result in symptomatic gastrointestinal reflux. Chronic diseases manifesting symptoms during REM sleep include angina, migraines, and cluster headaches.

REM sleep latency (the length of time from sleep onset to the first REM sleep period of the night) is often shorter in actively depressed patients. An increase in REM sleep latency has been correlated with improvements in psychometric depression scales and can be a marker for the efficacy of antidepressant medication.Nocturnal seizures, asthma, and panic attacks are more likely to occur in the NREM stages of sleep.

The sleep manifestations of posttraumatic stress disorder include stereotypic frightening dreams that occur either at sleep onset or during REM sleep. Such disordered dreaming can result in both sleep onset and sleep maintenance insomnia. Clinical Use of Sleep Stage and EEG EffectsMedication-induced changes in sleep stages can lead to an increase in symptoms occurring during those specific sleep/dream states. For example, insomnia and nightmares are associated with the REM sleep rebound that occurs after discontinuation of REM suppressive drugs (i.e., ethanol, barbiturates, benzodiazepines). Medications such as lithium that can increase deep sleep can induce the occurrence of arousal disorders such as somnambulism.The influence of psychoactive medications on sleep states has a positive side as well. For example, REM sleep suppressive medications can be useful adjuncts in the treatment of REM sleep parasomnias and symptoms. Both benzodiazepines and antidepressants can be used to decrease REM sleep.

Similarly, the arousal disorders can be treated with medications affecting deep sleep (benzodiazepines and others) (see and ). Respiratory EffectsCertain medications are known to affect respiratory drive.

Benzodiazepines, barbiturates, and narcotics can exacerbate respiratory failure in patients with COPD, central sleep apnea, and restrictive lung disease. These medications can also negatively affect obstructive sleep apnea. The newer hypnotics (zolpidem and zaleplon) have less respiratory suppressant effects. Medroxyprogesterone, protriptyline, and fluoxetine have been documented to have respiratory stimulant effects that may be clinically useful in some patients.

EnuresisEnuresis, defined as persistent bed-wetting more than twice a month past the age of 5 years, is present in 15% of 5-year-olds. Medication has been shown to be symptomatically useful. Tricyclic antidepressants have been used for decades in this disorder, but there has been concern about long-term safety in children.

The current treatment of choice is desmopressin nasal spray, which corrects the lack of cyclic antidiuretic hormone increase during sleep, typically seen in these patients. Symptoms can be controlled until neurophysiologic maturity occurs, bringing a resolution of nocturnal enuresis.

Restless Legs Syndrome and Periodic Limb Movement DisorderSymptoms of restless legs syndrome include uncomfortable limb sensations at sleep onset and motor restlessness exacerbated by relaxation. Periodic limb movement disorder is characterized by repetitive, stereotypic limb movements occurring in 15- to 40-second cycles in NREM sleep and often leading to recurrent arousals from sleep. These disorders are quite common, occurring in up to 15% of the population and increasing in frequency with age.Historically, both periodic limb movement disorder and restless legs syndrome have been treated with benzodiazepines, particularly clonazepam.

Low dosages of dopamine precursors and dopamine receptor agonists at bedtime have been demonstrated to be efficacious in these disorders. Possible side effects from these medications, which include carbidopa/levodopa, pergolide, pramipexole, selegiline, and ropinirole, are nausea, headache, and occasional augmentation of symptoms. Circadian Rhythm DisturbanceA number of sleep disorders are linked to abnormally timed sleep-wake cycles. These include delayed and advanced sleep phase syndromes in which the sleep period is markedly later or earlier than what is socially accepted, jet lag, shift work, and certain sleep abnormalities associated with aging. Melatonin is the photoneuroendocrine transducer that conveys information controlling sleep-wake cycles and circadian rhythms in the CNS. Low doses may be useful in treating these disorders. Because melatonin is marketed as a dietary supplement, there are minimal data on safety, side effects, and drug interactions for this compound. Ricky level editor game.

Jet lag and shift work disorders can also be effectively treated with short-term sedatives and hypnotics. CONCLUSIONA philosophy that remains cogent in regard to the CNS is that new research discoveries almost always show this system to be more complex than previously thought. Only a few years ago, if patients complained of difficulty sleeping, medications that were often dangerous and addictive were prescribed to induce sleep, while the basis of the patient's complaint was not addressed. Now sleeping pills are safer, and our understanding of the sleep state has increased exponentially. Reite ML, Nagel KE, and Ruddy JR. The Evaluation and Management of Sleep Disorders. Washington, DC: American Psychiatric Press.

1990. American Sleep Disorders Association. Thorpy MJ, ed. The International Classification of Sleep Disorders: Diagnosis and Coding Manual.

Lawrence, Kansas: Allen Press. 1990. Kryger MH, Roth T, and Dement WC. Principles and Practice of Sleep Medicine.

Philadelphia, Pa: WB Saunders. 1994. Wysowski DK, Baum C. Outpatient use of prescription sedative-hypnotic drugs in the United States, 1970 thought 1989.

Arch Intern Med. 1991; 151:1779–1783. Sateia MJ, Doghramji K, Hauri PJ, et al. Evaluation of chronic insomnia.

2000; 23:243–314. Mitler MM. Nonselective and selective benzodiazepine receptor agonists: where are we today? 2000; 23(suppl 1):S39–S47.

Aldrich MS. Automobile accidents in patients with sleep disorders. 1989; 12:487–494. Ray WA, Griffen MR, Downey W. Benzodiazepines of long and short elimination half-life and the risk of hip fracture. 1989; 262:3303–3307. Doghramji K.

The need for flexibility in dosing hypnotic agents. 2000; 23(suppl 1):S16–S20. Greenblatt DJ.

Benzodiazepine hypnotics: sorting the pharmacodynamic facts. J Clin Psychiatry.

1991; 52(9, suppl):4–10. Pagel JF. The treatment of insomnia.

1994; 49:1417–1422. George CFP. Perspectives in the management of insomnia in patients with chronic respiratory disorders. 2000; 23(suppl 1):S31–S35. Vermeeren A, Danjou PE, O'Hanlon JF.

Residual effects of evening and middle-of-the-night administration of zaleplon 10 and 20 mg on memory and actual driving performance. Hum Psychopharmacol Clin Exp. 1998; 13:S98–S107. Pagel JF, Zafralotfi S, Zammit G.

How to prescribe a good nights sleep. Patient Care.

1997 Feb; 31(4):87–94. Kessler RC, McGonagle KC, Zhao S. Epidemiology of psychiatric disorders. Arch Gen Psychiatry. 1994; 51:8–19. Richardson GS.

Managing insomnia in the primary care setting: raising the issues. 2000; 23(suppl 1):S9–S12.

Breslau N, Roth T, Rosenthal L, et al. Sleep disturbance and psychiatric disorder: a longitudinal epidemiological study of young adults. Biol Psychiatry. 1996; 39:411–418.

Weiler JM, Bloomfield JR, Woodworth GG, et al. Effects of fexofenadine, diphenhydramine, and alcohol on driving performance: a randomized, placebo controlled trial in the Iowa driving simulator.

Ann Intern Med. 2000; 132:354–363. Ancoli-Israel S. Insomnia in the elderly: a review for the primary care practitioner. 2000; 23(suppl 1):S23–S30. Ware JC, Brown FW, Moorad PJ, et al. Effects on sleep: a double blind study comparing trimipramine to imipramine in depressed insomniac patients.

1989; 12:537–549. Pagel JF. Disease, psychoactive medication, and sleep states. Primary Psychiatry. 1996; 3:47–51. Settle EC Jr.

Antidepressant drugs: disturbing and potentially dangerous adverse effects. J Clin Psychiatry. 1998; 59(suppl 16):25–30. Rickles K, Schweizer E, Clary C, et al. Nefazodone and imipramine in major depression: a placebo controlled trial. Br J Psychiatry.

1994; 164:802–805. Pagel JF. Pharmacologic alterations of sleep and dream: a clinical framework for utilizing the electrophysiological and sleep stage effects of psychoactive medications. Hum Psychopharmacol.

1996; 11:217–223. Current issues in the diagnosis and management of narcolepsy.

1998; 50(2, suppl 1):S1–S48. McClellan KJ, Spencer CM.

Modafinil: a review of its pharmacology and clinical efficacy in the management of narcolepsy. 1998; 9:311–324. Hauri PJ.

Current Concepts: The Sleep Disorders. Kalamazoo, Mich: The Upjohn Company. 1992.

Hart LL, Middleton RK, Schott WJ. Drug treatment for sleep apnea. DICP Ann Pharmacother. 1989; 23:308–315. Hermann WM.

Development and critical evaluation of an objective procedure for the electroencephalographic classification of psychotropic drugs. In: Hermann WM, ed. Electroencephalography in Drug Research. Stuttgart, Germany: Gustav Fisher. The discovery of psychotrophic drugs by computer-analyzed cerebral bioelectrical potentials (CEEG) Drug Dev Res.

1981; 1:373–407. Mamdema JW, Danhof M. Electroencephalogram effect measures and relationships between pharmacokinetics and pharmacodynamics of centrally acting drugs. Clin Pharmacokinet. 1992; 23:191–215. Armitage R, Rochlen A, Fitch T, et al.

Dream recall and major depression: a preliminary report. 1995; 5:189–198. Kupfer DJ, Ehlers CL, Frean E, et al. Resistant effects of antidepressants: EEG sleep studies in depressed patients during maintenance treatment. Biol Psychol.

1994; 35:781–793. Krakow B, Tandberg D, Barey M, et al. Nightmares and sleep disturbance in sexually assaulted women. 1995; 5:199–206. Pagel JF.

Nightmares and disorders of dreaming. 2000; 61:2037–2044. Pagel JF. Modeling drug actions on electrophysiologic effects produced by EEG modulated potentials. Hum Psychopharmacol. 1993; 8:211–216.

Schenck CH, Mahowald MW. Long-term, nightly benzodiazepine treatment of injurious parasomnias and other disorders of disrupted nocturnal sleep in 170 adults. 1996; 100:333–337. Klauber GT. Clinical efficacy and safety of desmopressin in the treatment of nocturnal enuresis. 1989 114(4, pt 2).

Walters AS. For the International Restless Legs Syndrome Study Group. Toward a better definition of the restless leg syndrome.

1995 10:634–642. Lavigne GJ, Montplaisir JY. Restless leg syndrome and sleep bruxism: prevalence and association among Canadians. 1994; 17:739–743. Boghen D, Lamothe L, Elie R, et al.

The treatment of restless leg syndrome with clonazepam: a prospective controlled study. Can J Neurol Sci. 1986; 13:245–247. Early CJ, Allen RP. Pergolide and carbidopa/levodopa treatment of the restless leg syndrome and periodic leg movements in sleep in a consecutive series of patients. 1996; 19:801–810.

Walker SL, Fine A, Kryger MH. L-DOPA/carbidopa for nocturnal movement disorders in uremia. 1996; 19:214–218. Stone BM, Turner C, Mills SL, et al. Hypnotic activity of melatonin. 2000; 23:663–670.

Arendt J, Middleton B, Stone B, et al. Complex effects of melatonin: evidence for photoperiodic responses in humans? 1999; 2:625–636. Buxton OM, Copinschi G, Van Onderbergen A, et al.

A benzodiazepine hypnotic facilitates adaptation of circadian rhythms and sleep-wake homeostasis to an eight hour delay shift simulating westward jet lag. 2000; 23:915–928.

Sleeping Pills and Natural Sleep Aids All you need to know about prescription and over-the-counter sleep medications—as well as effective insomnia treatments that don’t come in pill form. Are sleeping pills or sleep aids right for you?It’s the middle of the night, and you’re staring at the ceiling, thinking about work, or bills, or the kids. When sleep just won’t come, it’s tempting to turn to a sleeping pill or sleep aid for relief. And you may get it in the moment. But if you regularly have trouble sleeping, that’s a red flag that something’s wrong. It could be something as simple as too much caffeine or viewing TV, your phone, or other screens late at night. Or it may be a symptom of an underlying medical or psychological problem.

But whatever it is, it won’t be cured with sleeping pills. At best, sleeping pills are a temporary band aid. At worst, they’re an addictive crutch that can make insomnia worse in the long run.That doesn’t mean that you should never use medication, but it’s important to weigh the benefits against the risks. In general, sleeping pills and sleep aids are most effective when used sparingly for short-term situations, such as traveling across time zones or recovering from a medical procedure. If you choose to take sleeping pills over the long term, it is best to use them only on an infrequent, “as needed,” basis to avoid dependence and tolerance. Risks and side effects of sleeping pillsAll prescription sleeping pills have side effects, which vary depending on the specific drug, the dosage, and how long the drug lasts in your system.

Common side effects include prolonged drowsiness the next day, headache, muscle aches, constipation, dry mouth, trouble concentrating, dizziness, unsteadiness, and rebound insomnia. Other risks of sleeping pills include:Drug tolerance. You may, over a period of time, build up a tolerance to sleep aids, and you will have to take more and more for them to work, which in turn can lead to more side effects.Drug dependence. You may come to rely on sleeping pills to sleep, and will be unable to sleep or have even worse sleep without them. Prescription pills, in particular, can be very addictive, making it difficult to stop taking them.Withdrawal symptoms. If you stop the medication abruptly, you may have withdrawal symptoms, such as nausea, sweating, and shaking.Drug interactions.

Sleeping pills can interact with other medications. This can worsen side effects and sometimes be dangerous, especially with prescription painkillers and other sedatives.Rebound insomnia. If you need to stop taking sleeping pills, sometimes the insomnia can become even worse than before.Masking an underlying problem.

There may be an underlying medical or mental disorder, or even a sleep disorder, causing your insomnia that can’t be treated with sleeping pills. Some serious risks of sleeping pillsSedative-hypnotic medications (benzodiazepines and non-benzodiazepines) can cause severe allergic reaction, facial swelling, memory lapses, hallucinations, suicidal thoughts or actions, and complex sleep-related behaviors like sleep-walking, sleep-driving (driving while not fully awake, with no memory of the event) and sleep-eating (eating in the middle of the night with no recollection, often resulting in weight-gain).

If you experience any unusual sleep-related behavior, consult your doctor immediately. Over-the-counter (OTC) sleep aids and sleeping pillsStandard over-the-counter sleeping pills rely on antihistamines as their primary active ingredient to promote drowsiness. Common over-the-counter sleep medications include:. Diphenhydramine (found in brand names like Nytol, Sominex, Sleepinal, Compoz). Doxylamine (brand names such as Unisom, Nighttime Sleep Aid)Some other OTC sleep aids combine antihistamines with the pain reliever Acetaminophen (found in brand names like Tylenol PM and Aspirin-Free Anacin PM). Others, such as NyQuil, combine antihistamines with alcohol.The problem with antihistamines is that their sedating properties often last well into the next day, leading to a next-day hangover effect. When used long-term, they can also cause forgetfulness and headaches.

Because of these issues, sleep experts advise against their regular use. Common side effects of antihistamine sleeping pills:. Moderate to severe drowsiness the next day. Dizziness and forgetfulness. Clumsiness, feeling off balance. Constipation and urinary retention.

Blurred vision. Dry mouth and throat. NauseaPrescription sleep medicationsThere are several different types of prescription sleeping pills, classified as sedative hypnotics. In general, these medications act by working on receptors in the brain to slow down the nervous system. Some medications are used more for inducing sleep, while others are used for staying asleep.

Some last longer than others in your system (a longer half-life), and some have a higher risk of becoming habit forming. Benzodiazepine sedative hypnotic sleeping pillsBenzodiazepines are the oldest class of sleep medications still commonly in use. Benzodiazepines as a group are thought to have a higher risk of dependence than other insomnia sedative hypnotics and are classified as controlled substances.

Primarily used to treat anxiety disorders, benzodiazepines that have been approved to treat insomnia include estazolam (brand name ProSom), flurazepam (Dalmane), quazepam (Doral), temazepam (Restoril), and triazolam (Halcion). Drawbacks to benzodiazepine sleeping pills:You can become both physically and psychologically dependent on benzodiazepines. When you’re on the pills for a period of time, you may believe that you can’t sleep without them, and once you stop taking them, you may actually experience physical withdrawal symptoms like anxiety and rebound insomnia.Sleeping pills can lose their effectiveness if used on a nightly basis, because the brain receptors become less sensitive to their effects. In as little as three to four weeks, benzodiazepines can become no more effective than a sugar pill.The overall quality of your sleep can be reduced, with less restorative deep sleep and REM sleep.You may experience next day cognitive slowing and drowsiness (the hangover effect), which may be even worse than the sluggishness you feel from actual sleep deprivation.Insomnia returns once you stop, even if the medication is effective while taking it. As with the use of all sleeping pills, rather than dealing with your insomnia, you’re merely postponing the problem.There may be a link to dementia. While it’s currently under investigation, there is concern that using benzodiazepines may contribute to the development of dementia. Non-benzodiazepine sedative hypnotic sleeping pillsSome newer medications don’t have the same chemical structure as a benzodiazepine, but act on the same area in the brain.

They are thought to have fewer side effects, and less risk of dependency, but are still considered controlled substances. They include zalepon (Sonata), zolpidem (Ambien), and eszopiclone (Lunesta), which have been tested for longer-term use, up to six months. Drawbacks to non-benzodiazepine sleeping pills:Generally, non-benzodiazepines have fewer drawbacks than benzodiazepines, but that doesn’t make them suitable for everyone. Some may find this type of sleep medication ineffective at helping them sleep, while the long-term effects remain unknown. Food and Drug Administration (FDA) recently directed the manufacturers of Ambien and similar sleeping pills to lower the standard dosage due to the serious risk of morning grogginess while driving, especially in women patients. Other side effects include:.

Drug tolerance. Rebound insomnia. Headaches, dizziness, nausea, difficulty swallowing or breathing.

In some cases, dangerous sleep-related behaviors such as sleep-walking, sleep-driving, and sleep-eating. New or worsening depression; suicidal thoughts or actionsMelatonin receptor agonist hypnotic sleeping pillsRamelteon (Rozerem) is the newest type of sleep medication and works by mimicking the sleep regulation hormone melatonin. It has little risk of physical dependency but still has side effects. It is used for sleep onset problems and is not effective for problems regarding staying asleep.Ramelteon’s most common side effect is dizziness.

It may also worsen symptoms of depression and should not be used by those with severe liver damage. Antidepressants used as sleeping pillsThe FDA has not approved antidepressants for the treatment of insomnia, nor has their use been proven effective in treating sleeplessness. However, some antidepressants are prescribed off-label due to their sedating effects.

As with all depression medication, there is a small but significant risk of suicidal thoughts or worsening of depression, particularly in children and adolescents. Herbal and dietary sleep supplements that may helpGo the drugstore and you’ll see dozens of so-called “natural” sleep supplements. The FDA doesn’t regulate dietary supplements for safety, quality, effectiveness, or even truth in labeling, so it’s up to you to do your due diligence. Although the evidence is mixed, the following supplements have the most research backing them up as insomnia treatments.Valerian.

Valerian is a sedating herb that has been used since the second century A.D. To treat insomnia and anxiety. It is believed to work by increasing brain levels of the calming chemical GABA. Although the use of valerian for insomnia hasn’t been extensively studied, the research shows promise and it is generally considered to be safe and non-habit forming. It works best when taken daily for two or more weeks.Melatonin.

Melatonin is a naturally occurring hormone that increases at night. It is triggered by darkness and its levels remain elevated throughout the night until suppressed by the light of morning. Although melatonin does not appear to be particularly effective for treating most sleep disorders, it can help sleep problems caused by jet lag and shift work. Simple exposure to light at the right time, however, might be just as effective. If you take melatonin, be aware that it can interfere with certain blood pressure and diabetes medications. It’s best to stick with low doses—1 to 3 milligrams for most people—to minimize side effects and next-day drowsiness.Chamomile.

Many people drink chamomile tea for its gentle sedative properties, although it may cause allergic reactions in those with plant or pollen allergies. To get the full sleep-promoting benefit, bring water to a boil, then add 2-3 tea bags (or the equivalent of loose-leaf tea), cover with a lid, and brew for 10 minutes.Tryptophan. Tryptophan is a basic amino acid used in the formation of the chemical messenger serotonin, a substance in the brain that helps tell your body to sleep.

L-tryptophan is a common byproduct of tryptophan, which the body can change into serotonin. Some studies have shown that L-tryptophan can help people fall asleep faster. Results, however, have been inconsistent.Kava.

Kava has been shown to improve sleep in people with stress-related insomnia. However, kava can cause liver damage, so it isn’t recommended unless taken under close medical supervision.Other herbs that have been found to have a calming or sedating effect include lemon balm, passionflower, and lavender.

Many natural sleep supplements, such as MidNite and Luna, use a combination of these ingredients to promote sleep. Natural doesn’t mean safeWhile some remedies, such as lemon balm or chamomile tea are generally harmless, others can have more serious side effects and interfere with or reduce the effectiveness of prescribed medications. Valerian, for example, can interfere with antihistamines and statins. Do your research before trying a new herbal remedy and talk with your doctor or pharmacist if you have any pre-existing conditions or prescriptions that you take. Tips for safer use of sleeping pillsIf you decide to try sleeping pills or sleep aids, keep the following safety guidelines in mind.Never mix sleeping pills with alcohol or other sedative drugs. Alcohol not only disrupts sleep quality, but it increases the sedative effects of sleeping pills. The combination can be quite dangerous—even deadly.Only take a sleeping pill when you will have enough time for at least 7 to 8 hours of sleep.

Otherwise you may feel very drowsy the next day.Don’t take a second dose in the middle of the night. It can be dangerous to double up on your dosage, and with less time for the medication to clear your system it may be difficult to get up the next morning and shake off grogginess.Start with the lowest recommended dose. See how the medication affects you and the types of side effects you experience.Avoid frequent use. To avoid dependency and minimize adverse effects, try to save sleeping pills for emergencies, rather than nightly use.Never drive a car or operate machinery after taking a sleeping pill. This tip is especially important when you start using a new sleep aid, as you may not know how it will affect you.Carefully read the package insert that comes with your medication. Pay careful attention to the potential side effects and drug interactions. Many common medications, including antidepressants and antibiotics, can cause dangerous interactions with both prescription and over-the-counter sleeping pills.

For many sleeping pills, certain foods such as grapefruit and grapefruit juice must also be avoided. Talk to your doctor or pharmacist about:.

Other medications and supplements you are taking. Many common medications, including antidepressants and antibiotics, can cause dangerous interactions with both prescription and over-the-counter sleeping pills. Herbal and dietary supplements and non-prescription medications such as pain relievers and allergy medicines may also interfere. Other medical conditions you have. Some sleep medications can have serious side effects for people with medical problems such as high blood pressure, liver problems, glaucoma, depression, and breathing difficulties. Specific instructions for increasing, decreasing and/or terminating use.

It’s important to follow usage directions closely. Increasing your dose may pose risks, but decreasing your use can also cause problems if done too quickly. In some cases, stopping medication abruptly can cause uncomfortable side effects and even rebound insomnia.For better sleep, opt for healthy habits, not pillsResearch has shown that changing your lifestyle and sleep habits is the best way to combat insomnia. Even if you decide to use sleeping pills or medications in the short term, experts recommend making changes to your lifestyle and bedtime behavior as a long-term remedy to sleep problems. Behavioral and environmental changes can have more of a positive impact on sleep than medication, without the risk of side effects or dependence.

Relaxation techniques as an alternative to sleeping pillsthat can relieve stress and help you sleep include simple meditation practices, progressive muscle relaxation, yoga, tai chi, and the use of deep breathing. With a little practice, these skills can help you unwind at bedtime and improve your sleep more effectively than a sleeping pill or sleep aid. Try:A relaxing bedtime routine. Turn off screens at least one hour before bed and focus on quiet, soothing activities, such as reading, gentle yoga, or listening to soft music instead.

Keep the lights low to naturally boost melatonin.Abdominal breathing. Most of us don’t breathe as deeply as we should. When we breathe deeply and fully, involving not only the chest, but also the belly, lower back, and ribcage, it can actually help the part of our nervous system that controls relaxation. Close your eyes and try taking deep, slow breaths, making each breath even deeper than the last. Breathe in through your nose and out through your mouth. Make each exhale a little longer than each inhale.Progressive muscle relaxation is easier than it sounds. Lie down or make yourself comfortable.

Starting with your feet, tense the muscles as tightly as you can. Hold for a count of 10, and then relax. Continue to do this for every muscle group in your body, working your way up to the top of your head.

Exercise is a powerful sleep aidStudies have shown that can improve sleep at night. When we exercise, we experience a significant rise in body temperature, followed a few hours later by a significant drop. This drop in body temperature makes it easier for us to fall and stay asleep. The best time to exercise is late afternoon or early evening, rather than just before bed.

Aim for at least 30 minutes four times a week. Aerobic exercises are the best to combat insomnia as they increase the amount of oxygen that reaches the blood.

Cognitive behavioral therapy (CBT) beats sleeping pillsMany people complain that frustrating, negative thoughts and worries prevent them from sleeping at night.is a form of psychotherapy that treats problems by modifying negative thoughts, emotions, and patterns of behavior. A study at Harvard Medical School even found that CBT was more effective at treating chronic insomnia than prescription sleep medication—but without the risks or side effects. CBT can help to relax your mind, change your outlook, improve your daytime habits, and set you up for a good night’s sleep. – A guide to a good night’s rest.

(Harvard Medical School Special Health Report)– Including guidelines on using sleep medications and sleeping pills safely and properly. (American Academy of Sleep Medicine)– Common uses of sleeping pills, sleep medications, and other effective treatments for insomnia. (Mayo Clinic)– Guidelines for how to be safe when taking sleeping pills. (American Academy of Sleep Medicine)– Review of OTC sleep aids and herbal supplements. (Mayo Clinic)– Melatonin’s effects on insomnia. (National Sleep Foundation)– Use of valerian for treating insomnia and other sleep disorders. (Office of Dietary Supplements, National Institutes of Health)– Benefits of CBT versus popular sleep medications.

(Mayo Clinic)Authors: Melinda Smith, M.A., Lawrence Robinson, and Robert Segal, M.A. Last updated: June 2019.