Literature DB >> 9152562

The nonnarcotic antitussive drug dimemorfan: a review.

H Ida1.   

Abstract

The antitussive dimemorfan phosphate was discovered through extensive screening of morphinic derivatives and was introduced in Japan in 1975. The majority of studies on dimemorfan have been published in Japanese, and this review aims to make these data more generally available. The antitussive action of dimemorfan appears to be directly on the cough center in the medulla. Dimemorfan does not induce any significant physical or psychologic dependence, and its antitussive action is not affected by the opioid-receptor blocker levallorphan. Dimemorfan is therefore considered a nonnarcotic antitussive. Studies of antitussive effects in animal models indicate that dimemorfan is up to three times more potent than codeine and is equivalent to dextromethorphan. Three major comparative clinical trials and postmarketing surveillance studies showed that dimemorfan is equally or slightly more efficacious than dextromethorphan, benproperine phosphate, or placebo for the control of coughing. Several animal and clinical studies have confirmed the efficacy and safety of dimemorfan. Dimemorfan was effective in the majority of patients. In contrast to the narcotic antitussives, dimemorfan caused no serious problems with the digestive system, such as constipation and disorders of the bile duct, caused no dependence or tolerance, and was unlikely to have clinical analgesic effects. Minor side effects, such as loss of appetite, nausea, and drowsiness, were seen in less than 10% of patients. A syrup formulation of dimemorphan that retains its efficacy and safety is also available. Overall, these data indicate that dimemorfan is an effective nonnarcotic antitussive agent with a low incidence of adverse events.

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Year:  1997        PMID: 9152562     DOI: 10.1016/s0149-2918(97)80111-7

Source DB:  PubMed          Journal:  Clin Ther        ISSN: 0149-2918            Impact factor:   3.393


  6 in total

1.  Cytochrome P450 2D6*10 genotype affects the pharmacokinetics of dimemorfan in healthy Chinese subjects.

Authors:  Qi Pei; Jinfu Peng; Hongyi Tan; Liu Yang; Xiding Yang; Li Liu; Shikun Liu; Hong Yuan; Guoping Yang
Journal:  Eur J Drug Metab Pharmacokinet       Date:  2014-08-27       Impact factor: 2.441

2.  The dextromethorphan analog dimemorfan attenuates kainate-induced seizures via sigma1 receptor activation: comparison with the effects of dextromethorphan.

Authors:  Eun-Joo Shin; Seung-Yeol Nah; Won-Ki Kim; Kwang Ho Ko; Wang-Kee Jhoo; Yong-Kwang Lim; Joo Young Cha; Chieh-Fu Chen; Hyoung-Chun Kim
Journal:  Br J Pharmacol       Date:  2005-04       Impact factor: 8.739

3.  Pharmacokinetics of dimemorfan phosphate tablets in healthy Chinese volunteers.

Authors:  Yali Shen; Zhu Luo; Qin Yu; Ying Wang; Jin Xiang; Jia Miao
Journal:  Eur J Clin Pharmacol       Date:  2017-02-28       Impact factor: 2.953

4.  Anti-amnesic effect of dimemorfan in mice.

Authors:  Hui-Hung Wang; Jyh-Wei Chien; Yueh-Ching Chou; Jyh-Fei Liao; Chieh-Fu Chen
Journal:  Br J Pharmacol       Date:  2003-03       Impact factor: 8.739

5.  Survey of potentially inappropriate prescriptions for common cold symptoms in Japan: A cross-sectional study.

Authors:  Yasuhisa Nakano; Takashi Watari; Kazuya Adachi; Kenji Watanabe; Kazuya Otsuki; Yu Amano; Yuji Takaki; Kazumichi Onigata
Journal:  PLoS One       Date:  2022-05-12       Impact factor: 3.752

6.  Sigma-1 receptor attenuates osteoclastogenesis by promoting ER-associated degradation of SERCA2.

Authors:  Xiaoan Wei; Zeyu Zheng; Zhenhua Feng; Lin Zheng; Siyue Tao; Bingjie Zheng; Bao Huang; Xuyang Zhang; Junhui Liu; Yilei Chen; Wentian Zong; Zhi Shan; Shunwu Fan; Jian Chen; Fengdong Zhao
Journal:  EMBO Mol Med       Date:  2022-05-25       Impact factor: 14.260

  6 in total

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