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Oxazepam

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Oxazepam chemical structure
Oxazepam

(RS)-9-chloro-4-hydroxy-6-phenyl-
2,5-diazabicyclo[5.4.0]undeca-
5,8,10,12-tetraen-3-one

IUPAC name
CAS number
604-75-1
ATC code

N05BA04

PubChem
4616
DrugBank
APRD01152
Chemical formula {{{chemical_formula}}}
Molecular weight 286.71
Bioavailability 95.5%
Metabolism Hepatic
Elimination half-life 4-14 hours
Excretion Renal
Pregnancy category  ?
Legal status Schedule IV(US)
Routes of administration Oral


Oxazepam (marketed in English speaking countries under the following brand names Alepam, Medopam, Murelax, Noripam, Ox-Pam, Purata, Serax and Serepax), is a drug which is a benzodiazepine derivative.[1] Oxazepam is a benzodiazepine used extensively since the 1960s for the treatment of anxiety and insomnia and in the control of symptoms of alcohol withdrawal. It is a metabolite of diazepam, prazepam and temazepam.[2] Oxazepam has moderate anxiolytic, anticonvulsant, hypnotic, sedative and skeletal muscle relaxant properties compared to other benzodiazepines.[3]

IndicationsEdit

It is an intermediate acting benzodiazepine with a slow onset of action, so it is usually prescribed to individuals who have trouble staying asleep, rather than falling asleep. It is commonly prescribed for anxiety disorders with associated tension, irritability, and agitation. It is also prescribed for drug and alcohol withdrawal, and for anxiety associated with depression. Physicians may use Serax outside its approved indications to treat social phobia, posttraumatic stress disorder, insomnia, premenstrual syndrome, and other conditions.[4]

File:Oxazepam DOJ.jpg

DosageEdit

  • Mild/moderate anxiety - 10 to 15 mg, 3 to 4 times daily
  • Severe anxiety - 15 to 30 mg, 3 to 4 times daily
  • Symptoms related to alcohol withdrawal - 15 to 30 mg, 3 to 4 times daily

AvailabilityEdit

In the United Kingdom, oxazepam is available generically in the form of 10 mg, 15 mg and 30 mg tablets. In Finland, oxazepam is available generically in the form of 15 mg, 30 mg and 50 mg tablets.

UsageEdit

Oxazepam along with diazepam, nitrazepam and temazepam, were the four benzodiazepines listed on the pharmaceutical benefits scheme and represented 82% of the benzodiazepine prescriptions in Australia in 1990-1991.[5]

Side effectsEdit

The side effects of oxazepam are similar in nature to those of other benzodiazepines.

Side effects may include: Dizziness, drowsiness, headache, memory impairment, paradoxical excitement, transient global amnesia.

Side effects due to rapid decrease in dose or abrupt withdrawal from oxazepam may include: Abdominal and muscle cramps, convulsions, depression, inability to fall asleep or stay asleep, sweating, tremors, vomiting[6], or death.

ContraindicationsEdit

Oxazepam is contraindicated in Myasthenia gravis, chronic obstructive pulmonary disease and limited pulmonary reserve, as well as severe hepatic disease.

Special precautionsEdit

Benzodiazepines require special precaution if used in the elderly, during pregnancy, in children, alcohol- or drug-dependent individuals and individuals with comorbid psychiatric disorders.[7] Benzodiazepines including oxazepam are lipophilic drugs and rapidly penetrate membranes and therefore rapidly cross over into the placenta with significant uptake of the drug. Use of benzodiazepines in late pregnancy especially high doses may result in floppy infant syndrome.[8]

PregnancyEdit

Oxazepam when taken during late in pregnancy, the third trimester, causes a definite risk to the neonate including a severe benzodiazepine withdrawal syndrome in the neonate with symptoms including hypotonia, and reluctance to suck, to apnoeic spells, cyanosis, and impaired metabolic responses to cold stress. Floppy infant syndrome and sedation in the new born may also occur. Symptoms of floppy infant syndrome and the neonatal benzodiazepine withdrawal syndrome have been reported to persist from hours to months after birth.[9]

Tolerance, dependence and withdrawalEdit

Oxazepam as with other benzodiazepine drugs can cause tolerance, physical dependence, addiction and what is known as the benzodiazepine withdrawal syndrome. Withdrawal from oxazepam or other benzodiazepines often leads to withdrawal symptoms which are similar to those seen during alcohol and barbiturate withdrawal. The higher the dose and the longer the drug is taken the greater the risk of experiencing unpleasant withdrawal symptoms. Withdrawal symptoms can however occur at standard dosages and also after short term use. Benzodiazepine treatment should be discontinued as soon as possible via a slow and gradual dose reduction regimen.[10]

PharmacologyEdit

Oxazepam is an intermediate acting benzodiazepine. Oxazepam acts on benzodiazepine receptors resulting in increased effect of GABA to the GABAA receptor which results in inhibitory effects on the central nervous system.[11][12] The half-life of oxazepam is 4–15 hours.[13] Oxazepam has been shown to suppress cortisol levels.[14]

Oxazepam is an active metabolite formed during the breakdown of diazepam, nordazepam, and certain similar drugs. Oxazepam may be safer than many other benzodiazepines in patients with impaired liver function because it does not require hepatic oxidation, but rather it is simply metabolized via glucuronidation. This means that oxazepam is less likely to accumulate and cause adverse reactions in the elderly or people with liver disease. Oxazepam is similar to lorazepam in this respect. (1) There is preferential storage of oxazepam in some organs including the heart of the neonate. Absorption by any administered route and the risk of accumulation is significantly increased in the neonate and it is recommended to withdraw oxazepam during pregnancy and breast feeding as oxazepam is excreted in breast milk.[15]

InteractionsEdit

As oxazepam is an active metabolite of diazepam, there is likely an overlap in possible interactions with other drugs or food, with exception of the pharmacokinetic CYP450 interactions (e.g. with cimetidine). Take precautions, and follow closely the prescription of your doctor, when taking oxazepam (or other benozodiazepines) in combinations with antidepressant medication (SSRIs such as Prozac, Zoloft, and Paxil, or multiple reuptake inhibitors such as Wellbutrin, Cymbalta, or Effexor), potent painkillers (opioids, e.g. morphine, oxycodone or methadone). Concurrent use of these medicines (as well as other benzodiazepines) can interact in a way that is difficult to predict. Do not drink alcohol while taking oxazepam. Concomitant use of oxazepam and alcohol can lead to increased sedation, severe problems with coordination (ataxiae), decreased muscle tone and in severe cases or in predisposed patients even to life-threatening intoxications with respiratory depression, coma and collapse. Concomitant use of alcohol and oxazepam (as well as other benzodiazepines) also increases the risk of an addiction. [citation needed]

OverdoseEdit

Main article: Benzodiazepine overdose

Oxazepam is generally less toxic in overdose than other benzodiazepines.[16] Important factors which effect the severity of a benzodiazepine overdose include the dose injested, the age of the patient, health status prior to overdose. Benzodiazepine overdoses can be much more dangerous if there has been a coingestion of other CNS depressants such as opiates or alcohol. Symptoms of an oxazepam overdose include:[17][18][19]

AbuseEdit

Oxazepam is a drug with the potential for misuse. Drug misuse is defined as taking the drug to achieve a high, or continuing to take the drug in the long term against medical advice.[20] Benzodiazepines, including diazepam, oxazepam, nitrazepam, and flunitrazepam, accounted for the largest volume of forged drug prescriptions in Sweden 1982-1986. During this time, a total of 52% of drug forgeries were for benzodiazepines, suggesting benzodiazepines were a major prescription drug class of abuse.[21]

Legal StatusEdit

Oxazepam is a Schedule IV drug under the Convention on Psychotropic Substances [1].

CarcinogenicityEdit

Oxazepam is listed as a possible carcinogen (Group 2b) by the IARC.

See alsoEdit

ReferencesEdit

  1. Benzodiazepine Names. non-benzodiazepines.org.uk. URL accessed on 2008-12-29.
  2. Oxazepam (IARC Summary & Evaluation, Volume 66, 1996). IARC. URL accessed on 2009-03-12.
  3. Mandrioli R, Mercolini L, Raggi MA (October 2008). Benzodiazepine metabolism: an analytical perspective. Curr. Drug Metab. 9 (8): 827–44.
  4. http://www.psychatlanta.com/documents/serax.pdf
  5. Mant A, Whicker SD, McManus P, Birkett DJ, Edmonds D, Dumbrell D. (December 1993). Benzodiazepine utilisation in Australia: report from a new pharmacoepidemiological database. Aust J Public Health. 17 (4): 345–9.
  6. Oxazepam patient advice including side effects
  7. (November 2009). Benzodiazepine dependence: focus on withdrawal syndrome.. Ann Pharm Fr 67 (6): 408–13.
  8. Kanto JH. (May 1982). Use of benzodiazepines during pregnancy, labour and lactation, with particular reference to pharmacokinetic considerations. Drugs. 23 (5): 354–80.
  9. McElhatton PR. (Nov-Dec 1994). The effects of benzodiazepine use during pregnancy and lactation. Reprod Toxicol. 8 (6): 461–75.
  10. MacKinnon GL, Parker WA. (1982). Benzodiazepine withdrawal syndrome: a literature review and evaluation. The American journal of drug and alcohol abuse. 9 (1): 19–33.
  11. Skerritt JH, Johnston GA. (May 6, 1983). Enhancement of GABA binding by benzodiazepines and related anxiolytics. Eur J Pharmacol. 89 (3-4): 193–8.
  12. Oelschläger H. (July 4, 1989). [Chemical and pharmacologic aspects of benzodiazepines]. Schweiz Rundsch Med Prax. 78 (27-28): 766–72.
  13. Professor heather Ashton (2007). BENZODIAZEPINE EQUIVALENCY TABLE. URL accessed on September 23, 2007.
  14. Christensen P, Lolk A, Gram LF, Kragh-Sørensen P. (1992). Benzodiazepine-induced sedation and cortisol suppression. A placebo-controlled comparison of oxazepam and nitrazepam in healthy male volunteers. Psychopharmacology. 106 (4): 511–6.
  15. Olive G, Dreux C. (January 1977). Pharmacologic bases of use of benzodiazepines in peréinatal medicine. Arch Fr Pediatr. 34(1): 74–89.
  16. Buckley NA, Dawson AH, Whyte IM, O'Connell DL (28 January 1995). Relative toxicity of benzodiazepines in overdose. BMJ 310 (6974): 219–21.
  17. Gaudreault P, Guay J, Thivierge RL, Verdy I (1991). Benzodiazepine poisoning. Clinical and pharmacological considerations and treatment. Drug Saf 6 (4): 247–65.
  18. Perry HE, Shannon MW (June 1996). Diagnosis and management of opioid- and benzodiazepine-induced comatose overdose in children. Curr. Opin. Pediatr. 8 (3): 243–7.
  19. Busto U, Kaplan HL, Sellers EM (February 1980). Benzodiazepine-associated emergencies in Toronto. Am J Psychiatry 137 (2): 224–7.
  20. Griffiths RR, Johnson MW (2005). Relative abuse liability of hypnotic drugs: a conceptual framework and algorithm for differentiating among compounds. J Clin Psychiatry 66 Suppl 9: 31–41.
  21. Bergman U, Dahl-Puustinen ML. (1989). Use of prescription forgeries in a drug abuse surveillance network. Eur J Clin Pharmacol. 36 (6): 621–3.

External linksEdit



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