Tetrazepam

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Tetrazepam
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Systematic (IUPAC) name
7-Chloro-5-cyclohex-1-en-1-yl-1-methyl-1,3-dihydro-2H-1,4-benzodiazepin-2-one
Clinical data
Routes of
administration
Oral
Legal status
Legal status
  • Schedule IV US
Pharmacokinetic data
Biological half-life 3-26 hours
Identifiers
CAS Number 10379-14-3
ATC code M03BX07 (WHO)
PubChem CID 25215
ChemSpider 23551
Chemical data
Formula C16H17ClN2O
Molar mass 288.772[[Script error: No such module "String".]]
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Tetrazepam, (and is marketed under the following brand names, Clinoxan, Epsipam, Myolastan, Musaril, Relaxam and Spasmorelax) is a benzodiazepine derivative with anticonvulsant, anxiolytic, hypnotic and muscle relaxant properties. It is used mainly in Austria, France, Belgium, Germany and Spain to treat muscle spasm, anxiety disorders such as panic attacks, or more rarely to treat depression, premenstrual syndrome or agoraphobia. Tetrazepam has relatively little sedative effect at low doses while still producing useful muscle relaxation and anxiety relief.

Delayed type 4 allergic hypersensitivity reactions including aculopapular exanthema, erythematous rash, urticarial eruption, erythema multiforme, photodermatitis, eczema and Stevens-Johnson syndrome can occasionally occur as a result of tetrazepam exposure. These hypersensitivity reactions to tetrazepam share no cross-reactivity with other benzodiazepines.[1]

Indications

Tetrazepam is used therapeutically as a muscle relaxant.[2][3]

Availability

The indicated adult dose for muscle spasm is 50 mg three to four times per day, increased if necessary to a maximum of 800 mg per day, in divided doses. Tetrazepam is not generally recommended for use in children, except on the advice of a specialist.

Tetrazepam is only available in one strength and formulation, 50 mg tablets. The benzodiazepine equivalent of tetrazepam is approximately 5 mg of diazepam.[4]

Adverse effects

Allergic reactions to tetrazepam occasionally occur involving the skin.[1]

Allergic reactions can develop to tetrazepam[5][6] and it is considered to be a potential allergen.[7][8] Drug rash and drug-induced eosinophilia with systemic symptoms is a known complication of tetrazepam exposure.[9][10] These hypersensitive allergic reactions can be of the delayed type.[11][12][13]

Toxic epidermal necrolysis has occurred from the use of tetrazepam[14][15] including at least one reported death.[16] Stevens-Johnson syndrome and erythema multiforme has been reported from use of tetrazepam. Cross-reactivity with other benzodiazepines does not typically occur in such patients.[17][18][19] Exanthema[20] and eczema may occur.[21] The lack of cross-reactivity with other benzodiazepines is believed to be due to the molecular structure of tetrazepam.[22][23] Photodermatitis[24] and phototoxicity have also been reported.[25] Occupational contact allergy can also develop from regularly handling tetrazepam.[26][27] Airborne contact dermatitis can also occur as an allergy which can develop from occupational exposure.[28] Patch testing has been used successfully to demonstrate tetrazepam allergy.[29][30] Oral testing can also be used. Skin prick tests are not always accurate and may produce false negatives.[31]

Drowsiness is a common side effect of tetrazepam.[32] A reduction in muscle force can occur.[33] Myasthenia gravis, a condition characterised by severe muscle weakness is another potential adverse effect from tetrazepam.[34] Cardiovascular and respiratory adverse effects can occur with tetrazepam similar to other benzodiazepines.[23]

Tolerance, dependence and withdrawal

Prolonged use, as with all benzodiazepines, should be avoided, as tolerance occurs and there is a risk of benzodiazepine dependence and a benzodiazepine withdrawal syndrome after stopping or reducing dosage.[23]

Overdose

Tetrazepam, like other benzodiazepines is a drug which is very frequently used in overdoses. These overdoses are often mixed overdoses, i.e. a mixture of other benzodiazepines or other drug classes with tetrazepam.[35][36]

Contraindications and special caution

Benzodiazepines require special precaution if used in the elderly, during pregnancy, in children, alcohol or drug-dependent individuals and individuals with comorbid psychiatric disorders.[37]

Pharmacology

Tetrazepam is an unusual benzodiazepine in its molecular structure as it has cyclohexenyl group which has substituted the typical 5-phenyl moiety seen in other benzodiazepines.[38] Tetrazepam, is rapidly absorbed after oral administration, within 45 mins and reaches peak plasma levels in less than 2 hours. It is classed as an intermediate acting benzodiazepine with an elimination half-life of approximately 15 hours. It is primarily metabolised to the inactive metabolites 3-hydroxy-tetrazepam and norhydroxytetrazepam.[38][39] The pharmacological effects of tetrazepam are significantly less potent when compared against diazepam, in animal studies.[40] Tetrazepam is a benzodiazepine site agonist and binds unselectively to type 1 and type 2 benzodiazepine site types as well as to peripheral benzodiazepine receptors.[41] The muscle relaxant properties of tetrazepam are most likely due to a reduction of calcium influx.[42] Small amounts of diazepam as well as the active metabolites of diazepam are produced from metabolism of tetrazepam.[43][44] The metabolism of tetrazepam has led to false accusations of prisoners prescribed tetrazepam of taking illicit diazepam; this can lead to increased prison sentences for prisoners.[38]

Abuse

Tetrazepam as with other benzodiazepines is sometimes abused. It is sometimes abused to incapacitate a victim in order to carry out a drug-facilitated crime.[45] or abused in order to achieve a state of intoxication.[46] Tetrazepam's abuse for to carry out drug facilitated crimes may be less however, than other benzodiazepines due to its reduced hypnotic properties.[47]

See also

References

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  1. 1.0 1.1 Thomas, E; Bellón, T; Barranco, P; Padial, A; Tapia, B; Morel, E; Alves-Ferreira, J; Martín-Esteban, M (2008). "Acute generalized exanthematous pustulosis due to tetrazepam" (PDF). Journal of investigational allergology & clinical immunology : official organ of the International Association of Asthmology (INTERASMA) and Sociedad Latinoamericana de Alergia e Inmunologia. 18 (2): 119–22. ISSN 1018-9068. PMID 18447141. 
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  4. "Benzodiazepine Names". non-benzodiazepines.org.uk. Retrieved 2009-04-05. 
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  18. Sánchez, I; García-Abujeta, JL; Fernández, L; Rodríguez, F; Quiñones, D; Duque, S; López, R; Jerez, J (2 March 1998). "Stevens-Johnson syndrome from tetrazepam". Allergologia et immunopathologia. 26 (2): 55–7. ISSN 0301-0546. PMID 9645262. 
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  23. 23.0 23.1 23.2 Cabrerizo Ballesteros, S; Méndez Alcalde, JD; Sánchez Alonso, A (2007). "Erythema multiforme to tetrazepam" (PDF). Journal of investigational allergology & clinical immunology : official organ of the International Association of Asthmology (INTERASMA) and Sociedad Latinoamericana de Alergia e Inmunologia. 17 (3): 205–6. ISSN 1018-9068. PMID 17583114. 
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  25. Schwedler, S; Mempel, M; Schmidt, T; Abeck, D; Ring, J (1998). "Phototoxicity to tetrazepam - A new adverse reaction". Dermatology (Basel, Switzerland). 197 (2): 193–4. ISSN 1018-8665. PMID 9840980. 
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  31. Sánchez-Morillas, L; Laguna-Martínez, JJ; Reaño-Martos, M; Rojo-Andrés, E; Ubeda, PG (2008). "Systemic dermatitis due to tetrazepam" (PDF). Journal of investigational allergology & clinical immunology : official organ of the International Association of Asthmology (INTERASMA) and Sociedad Latinoamericana de Alergia e Inmunologia. 18 (5): 404–6. ISSN 1018-9068. PMID 18973107. 
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  35. Zevzikovas, A; Bertulyte, A; Dirse, V; Ivanauskas, L (2003). "Determination of benzodiazepine derivatives mixture by high performance liquid chromatography". Medicina (Kaunas, Lithuania). 39 Suppl 2: 30–6. ISSN 1010-660X. PMID 14617855. 
  36. Zevzikovas, A; Kiliuviene, G; Ivanauskas, L; Dirse, V (2002). "Analysis of benzodiazepine derivative mixture by gas-liquid chromatography" (PDF). Medicina (Kaunas, Lithuania) (in lithuanian). 38 (3): 316–20. ISSN 1010-660X. PMID 12474705. 
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  39. Baumgärtner, MG; Cautreels, W; Langenbahn, H (1984). "Biotransformation and pharmacokinetics of tetrazepam in man". Arzneimittel-Forschung. 34 (6): 724–9. ISSN 0004-4172. PMID 6148954. 
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