Difference Between Xanax and Valium
Xanax is the trade name of alprazolam. Alprazolam is a short acting anxiolytic drug that is used or the treatment of various anxiety disorders like panic disorder, general anxiety disorders and social anxiety disorders. It belongs to the benzodiazepine class and binds strongly to GABA A receptors. Alprazolam is a chemical analogue of triazolam which differs in the absence of a chlorine atom at the o-position of the6- phenyl ring. Further, the molecule acts as a sedative and anticonvulsant agent. The peak effects are achieved within 1.5 to 1.6 hours in case of panic disorder. The common side effects include sedation, drowsiness, hypotension and impaired balance. The drug is associated with potential withdrawal symptoms as it may cause habit forming property. Further the drug can cause CNS (Central Nervous System depression).
Valium is the trade name of diazepam, which is also a benzodiazepine. The indications of Valium are anxiety, withdrawal symptoms related to alcohol and other benzodiazepines, muscle spasms, seizures, insomnia and restless leg syndrome. The drug is also used to cause memory loss, especially in conditions like post traumatic stress disorder. Common side effects include sleepiness and lack of co-ordination. However, severe side effects are rare and may include suicidal thoughts and increased risk of seizures.
Both the above drugs act on the GABA-A receptors. These receptors are ligand gated chloride channels. Hence when such drug on these receptors, entry of chloride ions takes place in the post-synaptic membrane and causes its hyperpolarisation. Hence the drugs act to reduce the firing of action potential in the subsequent neurones and cause a calming effect on the mind. These drugs act on the limbic system structures that are associated with emotion and learning. The GABA-A receptor is a heterodimer and consists of alpha, beta and gamma subunits, which are responsible for specific actions like sedation, myorelaxant, memory loss (anterograde amnesia) and anticonvulsive actions. Detailed comparisons of both these drugs are explained below:
Features | Valium(diazepam) | Xanax(alprazolam) |
Chemical Compound | Benzodiazepine | Benzodiazepine |
Chemical structure | ||
Mechanism of Action | GABA-A receptor agonists and stimulates entry of Chloride ions in adjacent neurones and inhibits them | GABA-A receptor agonists and stimulates entry of Chloride ions in adjacent neurones and inhibits them |
Increases dopamine concentration in striatum | No | Yes |
Indications | Mainly used to treat insomnia associated with anxiety, alcohol withdrawal syndrome and panic attacks. Also used to treat vertigo, tetanus, adjunct treatment for paraplegia or tetraplegia | Various anxiety and anxiety related disorders like GAD, Panic Disorders. It is primarily an anxiolytic |
Suppresses Hypothalamus Pituitary adrenal axis | weakly | strongly |
Used to treat Benzodiazepine withdrawal symptom | Yes | No |
Treatment of Status Epilepticus | Used as First line therapy and acts as potent anticonvulsant | Not recommended, as it can cause seizures |
Treatment of Eclampsia | Yes | No |
Contraindications | Ataxia ( loss of gait), hypoventilation, hepatic problems, dialysis, Pregnant women, coma and severe depression, myasthenia gravis | Dizziness, Hypotension and loss of balance. Must not be given with alcohol |
Pediatric use | Not recommended below 18 years of age, except for epilepsy | May be given below 18 years with medical supervision |
Elderly patients | May cause cardiac arrest , hence should be administered with care and monitoring with individuals suffering from cardiac ailments | Can be given in elderly |
Withdrawal symptoms | Not severe, as the elimination half life is prolonged | Mean plasma elimination half life is shorter about 11.2 hours |
Side effects | Depression, sedation | Jaundice, hallucinations and sedation |
Drug Dependence | Low | High |
Route of administration | Orally, IV (in diluted form) and IM and suppository. The IM route has slow absorption. | Mainly oral |
Onset of Action | Very fast within 5 minutes and 15-30 minutes of IV administration and IM respectively | Slow release |
Peak effects | Within 15 minutes to one hour | 1.5-1.6 hours or even weeks |
Bioavailability | Very high | Lesser |
Protein Binding | 96-99% | 80% |
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References :
[0]Calcaterra, NE; Barrow, JC (16 April 2014). "Classics in chemical neuroscience: diazepam (valium).". ACS chemical neuroscience 5 (4): 253–60
[1]Mandrioli, R.; Mercolini, L.; Raggi, M. A. (2008). "Benzodiazepine Metabolism: An Analytical Perspective". Current Drug Metabolism 9 (8): 827–844.
[2]https://commons.wikimedia.org/wiki/File:Opakowanie_oraz_tabletka_Xanax_SR_0,5.jpg
i presently take take DIAZEPAM 5 MG PO FOR SPASTICITY PRN (as needed) related to my multiple sclerosis. I find it to be very effective as a skeletal muscle relaxer, especially in combination with my other muscle relaxers. I must state that I am under a doctor’s care and this is all done in concert with my doctors.