Diazepam definition is - a tranquilizer C16H13ClN2O used especially to relieve anxiety and tension and as a muscle relaxant.
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benzo diazep ine + -am (of unknown origin).
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Diazapam is a common misspelling of diazepam. Diazapam is is used in the treatment of anxiety disorders and for short-term relief of the symptoms of anxiety.
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Diazepam (diazapam) is also used to relieve the symptoms of acute alcohol withdrawal, to relax muscles, to relieve the uncontrolled muscle movements caused by cerebral palsy and paralysis of the lower body and limbs, to control involuntary movement of the hands (athetosis), to relax tight, aching muscles, and, along with other medications, to treat convulsive disorders such as epilepsy.
Diazepam (diazapam) is used in the treatment of anxiety disorders and for short-term relief of the symptoms of anxiety.
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Diazapam is a common misspelling of diazepam (diazepam).
It works by slowing down the movement of chemicals in the brain. Diazepam (diazapam) belongs to a class of drugs called benzodiazepines. This results in a reduction in nervous tension (anxiety) and muscle spasm, and also causes sedation.
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Delorazepam, also known as chlordesmethyldiazepam and nordiclazepam, is a drug which is a more potent by weight than diazepam (1 mg delorazepam = 1 mg lorazepam = 10 mg diazepam), typical doses range from 0.5 mg - 2 mg.
Post-acute-withdrawal syndrome (PAWS) is a set of persistent impairments that occur after Another case report, reported similar phenomenon in a female patient who abruptly reduced her diazepam dosage from 30 mg to 5 mg per day.
The condition gradually improves over a period of time which can range from six months to several years in more severe cases.  
Symptoms can sometimes come and go with wave-like reoccurrences or fluctuations in severity of symptoms. Common symptoms include impaired cognition, irritability, depressed mood, and anxiety; all of which may reach severe levels which can lead to relapse.  
Symptoms occur intermittently, but are not always present. They are made worse by stress or other triggers and may arise at unexpected times and for no apparent reason.
Generalized epilepsy with febrile seizures plus (GEFS+) is a syndromic autosomal dominant. Benzodiazepines, such as Diazepam, potentiate GABA induced current. This potentiation is abolished in cells expressing the R43Q mutant subunit.
GEFS+ type 1 is a subtype of GEFS+ in which there are mutations in SCN1B, a gene encoding a sodium channel β subunit. The β subunit is required for proper channel inactivation. There are two known mutations in SCN1B that lead to GEFS+ (Figure 1). The first and best characterized of these mutations is C121W. This mutation alters a cysteine involved in a disulfide bond in the extracellular N-terminus of the protein. This extracellular region is similar to the cell adhesion molecule contactin and other cell adhesion molecules.