{"id":13405,"date":"2026-02-08T01:57:54","date_gmt":"2026-02-07T23:57:54","guid":{"rendered":"https:\/\/stonersmeds.com\/?post_type=product&p=13405"},"modified":"2026-03-02T06:30:40","modified_gmt":"2026-03-02T04:30:40","slug":"lexomil-bromazepam-6mg","status":"publish","type":"product","link":"https:\/\/stonersmeds.com\/nl\/shop\/lexomil-bromazepam-6mg\/","title":{"rendered":"Lexomil Bromazepam 6mg"},"content":{"rendered":"

Buy Lexomil (Bromazepam) 6mg online in USA.Bromazepam<\/b>, sold under many brand names, is a benzodiazepine<\/a>. It is mainly an anti-anxiety<\/a> agent with similar side effects to diazepam<\/a> (Valium). In addition to being used to treat anxiety or panic states, bromazepam may be used as a premedicant prior to minor surgery. Bromazepam typically comes in doses of 3\u00a0mg and 6\u00a0mg tablets.[2]<\/a><\/sup><\/p>\n

It was patented in 1961 by Roche<\/a> and approved for medical use in 1974.[3]<\/a><\/sup><\/p>\n

Medical uses<\/span><\/h2>\n

Treatment of severe anxiety<\/a>.[4]<\/a><\/sup> Despite certain side effects<\/a> and the emergence of alternative products (e.g. pregabalin<\/a>), benzodiazepine medication remains an effective way of reducing problematic symptoms, and is typically deemed effective by patients[5]<\/a><\/sup>[6]<\/a><\/sup> and medical professionals.[7]<\/a><\/sup>[8]<\/a><\/sup>[9]<\/a><\/sup> Similarly to other intermediate-acting depressants<\/a>, it may be used as hypnotic medication[10]<\/a><\/sup> or in order to mitigate withdrawal effects of alcohol consumption.[11]<\/a><\/sup>[12]<\/a><\/sup>[13]<\/a><\/sup><\/p>\n

Pharmacology<\/span><\/h2>\n
<\/a>
50 Pills of Lexotanil<\/i> (containing 6 mg of Bromazepam apiece) as sold by Hoffmann-La Roche<\/a> in Germany<\/a><\/figcaption><\/figure>\n

Bromazepam is a \u201cclassical\u201d benzodiazepine; other classical benzodiazepines include: diazepam<\/a>, clonazepam<\/a>, oxazepam<\/a>, lorazepam<\/a>, nitrazepam<\/a>, flurazepam<\/a>, and clorazepate<\/a>.[14]<\/a><\/sup> Its molecular structure is composed of a diazepine<\/a> connected to a benzene<\/a> ring and a pyridine<\/a> ring, the benzene ring having a single nitrogen<\/a> atom that replaces one of the carbon atoms in the ring structure.[15]<\/a><\/sup> It is a 1,4-benzodiazepine, which means that the nitrogens on the seven-sided diazepine ring are in the 1 and 4 positions.<\/p>\n

Bromazepam binds to the GABA<\/a> receptor GABAA<\/sub><\/a>, causing a conformational change and increasing the inhibitory effects of GABA. It acts as a positive modulator<\/a>, increasing the receptors\u2019 response when activated by GABA itself or an agonist (such as alcohol<\/a>). As opposed to barbital<\/a>, BZDs<\/a> are not GABA-receptor activators and rely on increasing the neurotransmitter\u2019s natural activity.[16]<\/a><\/sup> Bromazepam is an intermediate-acting benzodiazepine, is moderately lipophilic<\/a> compared to other substances of its class[17]<\/a><\/sup> and metabolised hepatically via oxidative pathways.[18]<\/a><\/sup> It does not possess any antidepressant or antipsychotic qualities.[19]<\/a><\/sup><\/p>\n

After night time administration of bromazepam a highly significant reduction of gastric acid secretion occurs during sleep followed by a highly significant rebound in gastric acid production the following day.[20]<\/a><\/sup><\/p>\n

Bromazepam alters the electrical status of the brain causing an increase in beta activity and a decrease in alpha activity in EEG recordings.[21]<\/a><\/sup><\/p>\n

Pharmacokinetics<\/span><\/h3>\n

Bromazepam is reported to be metabolized by a hepatic enzyme belonging to the Cytochrome P450<\/a> family of enzymes. In 2003, a team led by Oda Manami at Oita Medical University<\/a> reported that CYP3A4<\/a>, a member of the Cytochrome P450 family, was not the responsible enzyme since itraconazole<\/a>, a known inhibitor of CYP3A4, did not affect its metabolism.[22]<\/a><\/sup> In 1995, J. van Harten at the Solvay Pharmaceutical<\/a> Department of Clinical Pharmacology in Weesp<\/a> reported that fluvoxamine<\/a>, which is a potent inhibitor of CYP1A2, a less potent CYP3A4<\/a> inhibitor, and a negligible inhibitor of CYP2D6<\/a>, does inhibit its metabolism.[23]<\/a><\/sup><\/p>\n

The major metabolite of bromazepam is hydroxybromazepam,[22]<\/a><\/sup> which is an active agent too and has a half-life approximately equal to that of bromazepam.[citation needed<\/span><\/a><\/i>]<\/sup><\/p>\n

Side-effects<\/span><\/h2>\n

Bromazepam is similar in side effects to other benzodiazepines. The most common side effects reported are drowsiness, sedation, ataxia<\/a>, memory impairment, and dizziness.[24]<\/a><\/sup> Impairments to memory functions are common with bromazepam and include a reduced working memory<\/a> and reduced ability to process environmental information.[25]<\/a><\/sup>[26]<\/a><\/sup>[27]<\/a><\/sup> A 1975 experiment on healthy, male college students exploring the effects of four different drugs on learning capacity observed that taking bromazepam alone at 6\u00a0mg 3 times daily for 2 weeks impaired learning capacities significantly. In combination with alcohol, impairments in learning capacity became even more pronounced.[28]<\/a><\/sup> Various studies report impaired memory, visual information processing and sensory data and impaired psychomotor performance;[29]<\/a><\/sup>[30]<\/a><\/sup>[31]<\/a><\/sup> deterioration of cognition including attention capacity and impaired co-ordinative skills;[32]<\/a><\/sup>[33]<\/a><\/sup> impaired reactive and attention performance, which can impair driving skills;[34]<\/a><\/sup> drowsiness<\/a> and decrease in libido<\/a>.[35]<\/a><\/sup>[36]<\/a><\/sup> Unsteadiness after taking bromazepam is, however, less pronounced than other benzodiazepines such as lorazepam<\/a>.[37]<\/a><\/sup><\/p>\n

On occasion, benzodiazepines can induce extreme alterations in memory such as anterograde amnesia<\/a> and amnesic automatism<\/a>, which may have medico-legal consequences. Such reactions occur usually only at the higher dose end of the prescribing spectrum.[38]<\/a><\/sup><\/p>\n

Very rarely, dystonia<\/a> can develop.[39]<\/a><\/sup><\/p>\n

Up to 30% treated on a long-term basis develop a form of dependence, i.e. these patients cannot stop the medication without experiencing physical and\/or psychological benzodiazepine withdrawal symptoms<\/a>.<\/p>\n

Leukopenia<\/a> and liver-damage of the cholestatic type with or without jaundice (icterus) have additionally been seen; the original manufacturer Roche<\/a> recommends regular laboratory examinations to be performed routinely.<\/p>\n

Ambulatory patients should be warned that bromazepam may impair the ability to drive vehicles and to operate machinery. The impairment is worsened by consumption of alcohol, because both act as central nervous system depressants. During the course of therapy, tolerance to the sedative effect usually develops.<\/p>\n

Frequency and seriousness of adverse effects<\/span><\/h3>\n

As with all medication, the frequency and seriousness of side-effects varies greatly depending on quantities consumed.[40]<\/a><\/sup>[41]<\/a><\/sup> In a study about bromazepam\u2019s negative effects on psychomotor skills and driving ability, it was noted that 3\u00a0mg doses caused minimal impairment.[42]<\/a><\/sup> It also appeared that impairment may be tied to methods of testing more so than on the product\u2019s intrinsic activity.[43]<\/a><\/sup><\/p>\n

Moreover, side-effects other than drowsiness, dizziness and ataxia seem to be rare[44]<\/a><\/sup> and not experienced by more than a few percent of users. The use of other, comparable medication seems to display an identically moderate side-effect profile.[45]<\/a><\/sup>[46]<\/a><\/sup>[47]<\/a><\/sup><\/p>\n

<\/span>Tolerance, dependence and withdrawal<\/span><\/h3>\n

Prolonged use of bromazepam can cause tolerance and may lead to both physical and psychological dependence on the drug, and as a result, it is a medication which is controlled by international law. It is nonetheless important to note that dependence, long-term use and misuse occur in a minority of cases[48]<\/a><\/sup>[49]<\/a><\/sup>[50]<\/a><\/sup> and are not representative of most patients\u2019 experience with this type of medication.[51]<\/a><\/sup>[52]<\/a><\/sup><\/p>\n

It shares with other benzodiazepines the risk of abuse, misuse, psychological dependence<\/a> or physical dependence<\/a>.[53]<\/a><\/sup>[54]<\/a><\/sup> A withdrawal study demonstrated both psychological dependence and physical dependence on bromazepam including marked rebound anxiety<\/a> after 4 weeks chronic use. Those whose dose was gradually reduced experienced no withdrawal.[55]<\/a><\/sup><\/p>\n

Patients treated with bromazepam for generalised anxiety disorder were found to experience withdrawal symptoms such as a worsening of anxiety, as well as the development of physical withdrawal symptoms when abruptly withdrawn bromazepam.[56]<\/a><\/sup> Abrupt or over rapid withdrawal from bromazepam after chronic use even at therapeutic prescribed doses can lead to a severe withdrawal syndrome including status epilepticus<\/a> and a condition resembling delerium tremens<\/a>.[57]<\/a><\/sup>[58]<\/a><\/sup>[59]<\/a><\/sup><\/p>\n

Animal studies have shown that chronic administration of diazepam<\/a> (or bromazepam) causes a decrease in spontaneous locomotor activity, decreased turnover of noradrenaline<\/a> and dopamine and serotonin<\/a>, increased activity of tyrosine hydroxylase and increased levels of the catecholamines. During withdrawal of bromazepam or diazepam a fall in tryptophan, serotonin levels occurs as part of the benzodiazepine withdrawal syndrome<\/a>.[60]<\/a><\/sup> Changes in the levels of these chemicals in the brain can cause headaches, anxiety, tension, depression, insomnia, restlessness, confusion, irritability, sweating, dysphoria<\/a>, dizziness, derealization<\/a>, depersonalization, numbness\/tingling of extremities, hypersensitivity to light, sound, and smell, perceptual distortions, nausea, vomiting, diarrhea, appetite loss, hallucinations, delirium, seizures, tremor, stomach cramps, myalgia<\/a>, agitation, palpitations, tachycardia<\/a>, panic attacks, short-term memory loss, and hyperthermia.[61]<\/a><\/sup>[62]<\/a><\/sup><\/p>\n

Overdose<\/span><\/h3>\n
Main article: Benzodiazepine overdose<\/a><\/div>\n

Bromazepam is commonly involved in drug overdoses.[63]<\/a><\/sup> A severe bromazepam benzodiazepine overdose<\/a> may result in an alpha pattern coma type.[64]<\/a><\/sup> The toxicity of bromazepam in overdosage increases when combined with other CNS depressant drugs such as alcohol<\/a> or sedative hypnotic drugs.[65]<\/a><\/sup> Similarly to other benzodiazepines however, being a positive modulator of certain neuroreceptors and not an agonist<\/a>, the product has reduced overdose potential compared to older products of the barbiturate<\/a> class. Its consumption alone is very seldom fatal in healthy adults.[66]<\/a><\/sup>[67]<\/a><\/sup><\/p>\n

Bromazepam was in 2005 the most common benzodiazepine involved in intentional overdoses in France<\/a>.[68]<\/a><\/sup> Bromazepam has also been responsible for accidental poisonings in companion animals. A review of benzodiazepine poisonings in cats and dogs from 1991 to 1994 found bromazepam to be<\/p>\n

responsible for significantly more poisonings than any other benzodiazepine.[69]<\/a><\/sup><\/p>\n

Contraindications<\/span><\/h2>\n

Benzodiazepines require special precaution if used in elderly, pregnant, child, alcohol- or drug-dependent individuals and individuals with comorbid<\/a> psychiatric disorders<\/a>.[70]<\/a><\/sup><\/p>\n

Special populations<\/span><\/h3>\n