Clonazepam for pain due to muscle spasm in a patient with vertebral compression fractures caused by multiple myeloma: a case report

Akita, Kazuki; Kumakura, Yasutomo; Nakajima, Emi; Ishiguro, Hiroki; Iijima, Tetsuya

doi:10.1186/s40981-021-00477-1

Cited by 3 publications

(1 citation statement)

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“…Clonazepam is also prescribed for the treatment of panic disorder in patients with or without agoraphobia [ 8 ]. The pharmacological properties of clonazepam include antimanic, sedative, muscle relaxant, and anxiolytic effects, which are common in benzodiazepines [ 9 , 10 ].…”

Section: Introductionmentioning

confidence: 99%

Bioequivalence Study of Two Tablet Formulations of Clonazepam 2 mg: A Randomized, Open-Label, Crossover Study in Healthy Mexican Volunteers Under Fasting Conditions

Genis-Najera,

Sañudo-Maury

2023

Neurol Ther

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Introduction The prevalence of neurological disorders is high among the Mexican population. Clonazepam is primarily indicated to treat panic disorders, certain kinds of epilepsy such as status epilepticus, childhood motor seizures (petit mal absence, Lennox–Gastaut syndrome, and infantile spasms), anxiety, and muscle spasm. This study was performed to compare bioequivalence between two oral tablet formulations of clonazepam 2 mg in healthy Mexican volunteers under fasting conditions. Methods This phase I, randomized, open-label, two-treatment, crossover study included 30 healthy volunteers. Subjects were randomly assigned to either test or reference formulation of clonazepam 2 mg. Each study period was separated by 21-day washout period. Blood samples were collected at pre-dose and up to 72 h after drug administration. Clonazepam concentrations were determined using a validated ultra-flow liquid chromatography–tandem mass spectrometric method. Pharmacokinetic parameters were determined using a non-compartmental method. Two formulations were considered bioequivalent if geometric mean ratios (test/reference) were between 80% and 125%. Safety was evaluated by recording adverse events. Results Pharmacokinetic parameters were comparable between test and reference formulations. The mean maximum plasma concentration ( C max ) was ≈ 13 ng/mL, area under the plasma concentration–time curve from time 0 to last measurable concentration (AUC 0– t ) was ≈ 360 ng h/mL, time to reach maximum plasma concentration ( T max ) was ≈ 3 h, and elimination half-life ( t 1/2 ) was ≈ 43 h. Geometric mean ratios (90% confidence interval) of C max (99.2–115.3%), AUC 0– t (100.6–110.6%), and AUC 0–∞ (98.5–111.6%) were within the bioequivalence range. Seven non-serious adverse events (mostly asymptomatic hypotension) were recorded. Conclusion The test and reference formulations of clonazepam 2 mg were bioequivalent and well tolerated in healthy Mexican volunteers under fasting conditions. Protocol Authorization Number 213301410B0051 (Approved on April 13, 2021). Supplementary Information The online version contains supplementary material available at 10.1007/s40120-023-00567-5.

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Section: Introductionmentioning

confidence: 99%