Tramadol, sold under the brand name Ultram among others,[1] is an
opioidpain medication and a
serotonin–norepinephrine reuptake inhibitor (SNRI) used to treat moderately severe
pain.[3][13] When taken by mouth in an immediate-release formulation, the onset of pain relief usually begins within an hour.[3] It is also available by injection.[14] It is available in combination with
paracetamol (acetaminophen).
Tramadol was patented in 1972 and launched under the name "Tramal" in 1977 by the West German
pharmaceutical companyGrünenthal GmbH.[13][17] In the mid-1990s, it was approved in the United Kingdom and the United States.[13] It is available as a
generic medication and marketed under many brand names worldwide.[1][3] In 2021, it was the 41st most commonly prescribed medication in the United States, with more than 15million prescriptions.[18][19]
Medical uses
Tramadol is used primarily to treat mild to severe pain, both acute and chronic.[20][21] There is moderate evidence for use as a second-line treatment for
fibromyalgia but it is not FDA approved for this use.[22] Its use is approved for treatment of fibromyalgia as a secondary
painkiller by the
NHS.[23]
Its
analgesic effects take approximately an hour to be realized, and it takes from two to four hours to reach peak effect after oral administration with an immediate-release formulation.[20][21] On a dose-by-dose basis, tramadol has about one-tenth the potency of
morphine (thus 100 mg is commensurate with 10 mg morphine but may vary) and is practically equally potent when compared with
pethidine and
codeine.[24] For moderate pain, its effectiveness is roughly equivalent to that of codeine in low doses and
hydrocodone at very high doses. For severe pain it is less effective than morphine.[20]
Pain reducing effects last approximately six hours. The potency of analgesia varies considerably as it depends on an individual's genetics. People with specific variants of
CYP2D6 enzymes may not produce adequate amounts of the active metabolite (desmetramadol) for effective pain control.[12][20]
Sleep medicine physicians sometimes prescribe tramadol (or other opiate medications) for
refractoryrestless legs syndrome (RLS);[25][26] that is, RLS that does not respond adequately to treatment with first-line medications such as
dopamine agonists (like
pramipexole) or alpha-2-delta (α2δ) ligands (
gabapentinoids), often due to augmentation.[27]
Contraindications
Individuals with certain genetic variations of
CYP2D6 enzymes, which convert tramadol into an inactive molecule, may not experience enough pain relief from tramadol.[12][20] These
genetic polymorphisms are not currently routinely tested for in clinical practice.[28]
Pregnancy and lactation
Use of Tramadol during
pregnancy is generally avoided, as it may cause some reversible withdrawal effects in the newborn.[29] A small prospective study in France found, while an increased risk of
miscarriages existed, no major malformations were reported in the newborn.[29] Its use during
lactation is also generally advised against, but a small trial found that infants breastfed by mothers taking tramadol were exposed to about 2.88% of the dose the mothers were taking. No evidence of this dose harming the newborn was seen.[29]
Labor and delivery
Its use as an analgesic during labor is not advised due to its long onset of action (1 hour).[29] The ratio of the mean concentration of the drug in the fetus compared to that of the mother when it is given intramuscularly for labor pains has been estimated to be 1:94.[29]
Children
Its use in children is generally advised against, although it may be done under the supervision of a specialist.[20] On 21 September 2015, the FDA started investigating the safety of tramadol in use in persons under the age of 17. The investigation was initiated because some of these people have experienced slowed or difficult breathing.[30] The FDA lists age under 12 years old as a contraindication.[31][32]
Elderly
The risk of opioid-related adverse effects such as
respiratory depression, falls, cognitive impairment and sedation is increased.[20] Tramadol may interact with other medications and increase the risk for adverse events.[28]
Liver and kidney failure
The drug should be used with caution in those with liver or kidney failure, due to metabolism in the liver (to the active molecule desmetramadol) and elimination by the kidneys.[20]
Long-term use of high doses of tramadol causes
physical dependence and withdrawal syndrome.[36] These include both symptoms typical of
opioid withdrawal and those associated with
serotonin–norepinephrine reuptake inhibitor (SNRI) withdrawal; symptoms include numbness, tingling,
paresthesia, and tinnitus.[37] Psychiatric symptoms may include hallucinations, paranoia, extreme anxiety, panic attacks, and confusion.[38] In most cases, tramadol withdrawal will set in 12–20 hours after the last dose, but this can vary.[37] Tramadol withdrawal typically lasts longer than that of other opioids. Seven days or more of acute withdrawal symptoms can occur as opposed to typically 3 or 4 days for other codeine analogs.[37]
Overdose
The clinical presentation in overdose cases can vary but typically includes neurological, cardiovascular, and gastrointestinal manifestations.[39] The predominant neurological symptoms are
seizures and altered levels of consciousness, ranging from
somnolence to
coma. Seizures are particularly notable due to tramadol's lowering of the
seizure threshold, occurring in approximately half of acute poisoning cases.[40] Patients often exhibit
tachycardia and mild
hypertension. Gastrointestinal disturbances such as nausea and vomiting are common, and agitation, anxiety, and cold and clammy skin may also be present.[41]
While less common, severe complications like respiratory depression and
serotonin syndrome can occur, particularly in
polydrug overdoses involving other CNS depressants (such as
benzodiazepines, opioids, and alcohol) and agents with
serotonergic activity.[42][43] Additionally, Individuals with genetic variations leading to
CYP2D6 enzyme duplication (rapid metabolizers) may have an increased risk of adverse effects, due to faster conversion of tramadol to its active
metabolite.[44]
Acute tramadol overdose is generally not life-threatening, with most fatalities resulting from polysubstance overdose.[45] Management includes cardiovascular monitoring,
activated charcoal administration, hydration, and treatment of seizures.[46]Naloxone, an opioid antagonist, can partially reverse some effects of tramadol overdose, particularly respiratory depression. However, its use may increase the risk of seizures due to unopposed
alpha-adrenergic stimulation.[20] For suspected serotonin syndrome,
cyproheptadine, a
serotonin antagonist, is considered an effective antidote.[42]
The incidence of tramadol-related overdose deaths has been on the rise in certain regions. For instance, Northern Ireland has reported an increased frequency of such cases.[47] In 2013, England and Wales recorded 254 tramadol-related deaths, while Florida reported 379 cases in 2011.[48][49] In 2011, 21,649 emergency room visits in the United States were related to tramadol.[50] The likely explanation for these observations is due to increase in frequency of prescriptions and use due to easier access due to lighter
regulatory scheduling by authorities[51] but this is starting to change. In 2021,
Health Canada announced tramadol would be added to Schedule I of the
Controlled Drugs and Substances Act and to the Narcotic Control Regulations due to tramadol being suspected of having contributed to 18 reported deaths in Canada between 2006 and 2017.[52]
Tramadol is metabolized by
CYP2D6 enzymes which contribute to the metabolism of approximately 25% of all medications.[53] Any medications with the ability to inhibit or induce these enzymes may interact with tramadol. These include common antiarrhythmics, antiemetics, antidepressants (
sertraline,
paroxetine, and
fluoxetine in particular),[54] antipsychotics, analgesics, and tamoxifen.[55]
Due to tramadol's serotonergic effects, tramadol has the potential to contribute to the development of an acute or chronic hyper-serotonin state called
serotonin syndrome when used concurrently with other pro-serotonergic medications such as antidepressants (
SSRIs,
SNRIs,
tricyclics,
MAOIs),
antipsychotics,
triptans, cold medications containing
dextromethorphan, and some herbal products such as
St. John's wort.[55][56]
Tramadol increases the risk for seizures by lowering the seizure threshold. Using other medications that lower seizure threshold - such as
antipsychotic medications,
bupropion (an anti-depressant and smoking cessation drug), and
amphetamines - can further increases this risk.[59]
Pharmacology
Mechanism of action
Tramadol induces analgesic effects through a variety of different targets on the
noradrenergic system,
serotoninergic system, and
opioid receptors system.[60] Tramadol exists as a
racemic mixture, the positive
enantiomer inhibits serotonin reuptake while the negative enantiomer inhibits noradrenaline re-uptake, by binding to and blocking the transporters.[61][11] Tramadol has also been shown to act as a serotonin releasing agent. Both enantiomers of tramadol are agonists of the
μ-opioid receptor and its M1 metabolite, O-
desmetramadol, is also a μ-opioid receptor agonist but is 6 times more potent than tramadol itself.[62] All these effects work synergistically to induce analgesia.
Tramadol acts on the
opioid receptors through its major
active metabolitedesmetramadol, which has as much as 700-fold higher affinity for the MOR relative to tramadol.[16] Moreover, tramadol itself has been found to possess no
efficacy in activating the MOR in functional activity assays, whereas desmetramadol activates the receptor with high intrinsic activity (
Emax equal to that of
morphine).[71][16][88] As such, desmetramadol is exclusively responsible for the opioid effects of tramadol.[89] Both tramadol and desmetramadol have pronounced
selectivity for the MOR over the DOR and KOR in terms of binding affinity.[72][67][69]
Tramadol is well-established as an SRI.[64][65] In addition, a few studies have found that it also acts as a
serotonin releasing agent (1–10 μM), similar in effect to
fenfluramine.[90][91][92][93] The serotonin releasing effects of tramadol could be blocked by sufficiently high concentrations of the serotonin reuptake inhibitor
6-nitroquipazine, which is in accordance with other serotonin releasing agents such as fenfluramine and
MDMA.[90][92][93] However, two more recent studies failed to find a releasing effect of tramadol at respective concentrations up to 10 and 30 μM.[94][93][87] In addition to serotonergic activity, tramadol is also a
norepinephrine reuptake inhibitor.[64][65] It is not a
norepinephrine releasing agent.[95][96][97][87] Tramadol does not inhibit the reuptake or induce the release of
dopamine.[95][87]
A
positron emission tomographyimaging study found that single oral 50-mg and 100-mg doses of tramadol to human volunteers resulted in 34.7% and 50.2% respective mean occupation of the
serotonin transporter (SERT) in the
thalamus.[98] The estimated
median effective dose (ED50) for SERT occupancy hence was 98.1 mg, which was associated with a plasma tramadol level of about 330 ng/ml (1,300 nM).[98] The estimated maximum daily dosage of tramadol of 400 mg (100 mg
q.i.d.) would result in as much as 78.7% occupancy of the SERT (in association with a plasma concentration of 1,220 ng/ml or 4,632 nM).[98] This is close to that of SSRIs, which occupy the SERT by 80% or more.[98]
Peak plasma concentrations during treatment with clinical dosages of tramadol have generally been found to be in the range of 70 to 592 ng/ml (266–2,250 nM) for tramadol and 55 to 143 ng/ml (221–573 nM) for desmetramadol.[21] The highest levels of tramadol were observed with the maximum oral daily dosage of 400 mg per day divided into one 100-mg dose every 6 hours (i.e., four 100-mg doses evenly spaced out per day).[21][99] Some accumulation of tramadol occurs with chronic administration; peak plasma levels with the maximum oral daily dosage (100 mg
q.i.d.) are about 16% higher and the
area-under-the-curve levels 36% higher than following a single oral 100-mg dose.[21]Positron emission tomography imaging studies have reportedly found that tramadol levels are at least four-fold higher in the
brain than in
plasma.[95][100] Conversely, brain levels of desmetramadol "only slowly approach those in plasma".[95] The
plasma protein binding of tramadol is only 4–20%; hence, almost all tramadol in circulation is free, thus bioactive.[101][102][103]
Correspondence to effects
Co-administration of
quinidine, a potent CYP2D6 enzyme inhibitor, with tramadol, a combination which results in markedly reduced levels of desmetramadol, was found not to significantly affect the analgesic effects of tramadol in human volunteers.[16][102] However, other studies have found that the analgesic effects of tramadol are significantly decreased or even absent in CYP2D6 poor metabolizers.[16][89] The analgesic effects of tramadol are only partially reversed by
naloxone in human volunteers,[16] hence indicating that its opioid action is unlikely the sole factor; tramadol's analgesic effects are also partially reversed by
α2-adrenergic receptor antagonists such as
yohimbine, the
5-HT3 receptor antagonist
ondansetron, and the
5-HT7 receptor antagonists
SB-269970 and
SB-258719.[21][104] Pharmacologically, tramadol is similar to
tapentadol and
methadone in that it not only binds to the MOR, but also inhibits the reuptake of serotonin and norepinephrine[9] due to its action on the noradrenergic and serotonergic systems, such as its "atypical" opioid activity.[105]
Tramadol has inhibitory actions on the 5-HT2C receptor. Antagonism of 5-HT2C could be partially responsible for tramadol's reducing effect on depressive and
obsessive–compulsive symptoms in patients with pain and co-morbid neurological illnesses.[75] 5-HT2C blockade may also account for its lowering of the
seizure threshold, as 5-HT2Cknockout mice display significantly increased vulnerability to epileptic seizures, sometimes resulting in spontaneous death. However, the reduction of seizure threshold could be attributed to tramadol's putative inhibition of
GABAA receptors at high doses (significant inhibition at 100 μM).[84][61] In addition, desmetramadol is a high-affinity ligand of the DOR, and activation of this receptor could be involved in tramadol's ability to provoke seizures in some individuals, as DOR agonists are well known for inducing seizures.[69]
Nausea and
vomiting caused by tramadol are thought to be due to activation of the
5-HT3 receptor via increased serotonin levels.[73] In accordance, the 5-HT3 receptor antagonist
ondansetron can be used to treat tramadol-associated nausea and vomiting.[73] Tramadol and desmetramadol themselves do not bind to the 5-HT3 receptor.[73][65]
Pharmacokinetics
Tramadol is metabolised in the
liver via the
cytochrome P450isozymeCYP2B6,
CYP2D6, and
CYP3A4, being O- and N-demethylated to five different metabolites. Of these,
desmetramadol (O-desmethyltramadol) is the most significant, since it has 200 times the μ-affinity of (+)-tramadol, and furthermore has an elimination half-life of 9 hours, compared with 6 hours for tramadol itself. As with codeine, in the 6% of the population who have reduced CYP2D6 activity (hence reducing metabolism), a reduced analgesic effect is seen. Those with decreased CYP2D6 activity require a dose increase of 30% to achieve the same degree of pain relief as those with a normal level of CYP2D6 activity.[106][107]
Phase II
hepatic metabolism renders the metabolites water-soluble, which are excreted by the kidneys. Thus, reduced doses may be used in
renal and
hepatic impairment.[21]
Its
volume of distribution is around 306 L after oral administration and 203 L after parenteral administration.[21]
Chemistry
Tramadol is marketed as a
racemic mixture of both R- and S-
stereoisomers,[9] because the two isomers complement each other's analgesic activities.[9] The (+)-isomer is predominantly active as an opiate with a higher affinity for the µ-opiate receptor (20 times higher affinity than the (-)-isomer).[108]
Synthesis and stereoisomerism
(1R,2R)-tramadol
(1S,2S)-tramadol
(1R,2S)-tramadol
(1S,2R)-tramadol
The chemical synthesis of tramadol is described in the literature.[109] Tramadol [2-(dimethylaminomethyl)-1-(3-methoxyphenyl)cyclohexanol] has two stereogenic centers at the
cyclohexane ring. Thus, 2-(dimethylaminomethyl)-1-(3-methoxyphenyl)cyclohexanol may exist in four different configurational forms:
(1R,2R)-isomer
(1S,2S)-isomer
(1R,2S)-isomer
(1S,2R)-isomer
The synthetic pathway leads to the
racemate (1:1 mixture) of (1R,2R)-isomer and the (1S,2S)-isomer as the main products. Minor amounts of the racemic mixture of the (1R,2S)-isomer and the (1S,2R)-isomer are formed as well. The isolation of the (1R,2R)-isomer and the (1S,2S)-isomer from the
diastereomeric minor racemate [(1R,2S)-isomer and (1S,2R)-isomer] is realized by the recrystallization of the
hydrochlorides.
The drug tramadol is a racemate of the hydrochlorides of the (1R,2R)-(+)- and the (1S,2S)-(−)-enantiomers.
The resolution of the racemate [(1R,2R)-(+)-isomer / (1S,2S)-(−)-isomer] was described[110] employing (R)-(−)- or (S)-(+)-mandelic acid. This process does not find industrial application, since tramadol is used as a racemate, despite known different physiological effects[111] of the (1R,2R)- and (1S,2S)-isomers, because the racemate showed higher analgesic activity than either enantiomer in animals[112] and in humans.[113]
Detection in biological fluids
Tramadol and desmetramadol may be quantified in blood, plasma, serum, or saliva to monitor for abuse, confirm a diagnosis of poisoning or assist in the forensic investigation of a sudden death. Most commercial opiate immunoassay screening tests do not cross-react significantly with tramadol or its major metabolites, so chromatographic techniques must be used to detect and quantitate these substances. The concentration of desmetramadol in the blood or plasma of a person who has taken tramadol is generally 10–20% those of the parent drug.[114][115][116]
Society and culture
Formulations
Available dosage forms include liquids, syrups, drops, elixirs, effervescent tablets and powders for mixing with water, capsules, tablets including extended-release formulations, suppositories, compounding powder, and injections.[20]
Patent history
The U.S.
Food and Drug Administration (FDA) approved tramadol in March 1995, and an extended-release (ER) formulation in September 2005.[117] ER Tramadol was protected by US patents nos. 6,254,887[118] and 7,074,430.[119][120] The FDA listed the patents' expiration as 10 May 2014.[119] However, in August 2009, US District Court for the District of Delaware ruled the patents invalid, a decision upheld the following year by the Court of Appeals for the Federal Circuit. Manufacture and distribution of generic equivalents of Ultram ER in the United States was therefore permitted prior to the expiration of the patents.[121]
Legal status
Effective 18 August 2014, tramadol has been placed into
Schedule IV of the federal Controlled Substances Act in the United States.[122][123] Before that, some US states had already classified tramadol as a Schedule IV controlled substance under their respective state laws.[124][125][126]
Tramadol is classified in Schedule 4 (prescription only) in Australia, rather than as a
Schedule 8 Controlled Drug (Possession without authority illegal) like most other
opioids.[20]
On 10 June 2014, the United Kingdom's Home Office classified tramadol as a Class C, Schedule 3 controlled drug, but exempted it from the safe custody requirement.[128]
On 1 October 2023, New Zealand's Medsafe reclassified tramadol as a Class C2 Controlled Drug (in addition to its existing status as a prescription only medication).[129]
Misuse
Illicit use of the drug is thought to be a major factor in the success of the
Boko Haram terrorist organization.[130][131][132] When used at higher doses, the drug "can produce similar effects to heroin."[130] One former member said, "whenever we took tramadol, nothing mattered to us anymore except what we were sent to do because it made us very high and very bold, it was impossible to go on a mission without taking it."[130] Tramadol is also used as a coping mechanism in the
Gaza Strip.[133] It is also abused in the
United Kingdom, inspiring the title of the TV show Frankie Boyle's Tramadol Nights (2010).[134][135]
In 2013, researchers reported that tramadol was found in relatively high concentrations (1%+) in the roots of the African
pin cushion tree (Nauclea latifolia).[146] In 2014, however, it was reported that the presence of tramadol in the tree roots was the result of tramadol having been administered to cattle by farmers in the region:[147] tramadol and its
metabolites were present in the animals' excreta, which contaminated the soil around the trees. Therefore, tramadol and its mammalian metabolites were found in tree roots in the far north of
Cameroon, but not in the south where it is not administered to farm animals.[147]
A 2014 editorial in Lab Times online contested the notion that tramadol in tree roots was the result of anthropogenic contamination, stating that samples were taken from trees that grew in national parks, where livestock were forbidden; it also quoted researcher Michel de Waard, who stated that "thousands and thousands of tramadol-treated cattle sitting around a single tree and urinating there" would be required to produce the concentrations discovered.[148]
In 2015,
radiocarbon analysis confirmed that the tramadol found in N. latifolia roots could not be plant-derived and was of synthetic origin.[149]
Veterinary medicine
Tramadol may be used to treat post-operative, injury-related, and chronic (e.g., cancer-related) pain in dogs and cats as well as rabbits,
coatis, many small mammals including
rats and
flying squirrels,
guinea pigs,
ferrets, and
raccoons.[150]
Pharmacokinetics of tramadol across the species[150]
Species
Half-life (h) for parent drug
Half-life (h) for desmetramadol
Maximum plasma concentration (ng/mL) for parent drug
Maximum plasma concentration (ng/mL) for desmetramadol
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