Monograph
A07DA53 - Loperamide, Combinations |
Propably not porphyrinogenic |
PNP |
Rationale
Limitations: This safety classification applies only to preparations containing a combination of the two drugs loperamide and dimeticone. This same ATC-code (A07DA53) may in some countries be used for different combinations of loperamide and other drugs which in theory may be porphyrinogenic. Please refer to the classification and monograph of each individual substance. Loperamide has not shown to alter the pharmacokinetics of other drugs and is not suspected to influence the activity of hepatic cyp enzymes in vivo.
Dimeticone is a polymeric silicone devoid of Cyp-affinity and is not absorbed in the gastrointestinal tract.
Chemical description
Loperamide hydrochloride (chlorophenyl hydroxypiperidine dimethyl phenylbutylamide). One cyclic and one terminal tertiary nitrogen function. Simeticon (activated dimeticone; permethyl polysiloxane); Polymer with a structure of alternate atoms of silicon dioxide and liquid silicone. Practically insoluble in water. Water repellent, diminishing surface tension.
Therapeutic characteristics
Loperamide in combination with dimeticone is indicated for the symptomatic treatment of acute diarrhoea with dyspepsia caused by abdominal disconfort and flatulence.
Hepatic exposure
Not significant
Metabolism and pharmacokinetics
About 40 per cent of the oral dose of loperamide is absorbed from the gastrointestinal tract. Substrate of P-gp. It is excreted as conjugates via bile, mainly or partly after Cyp3A4 and 2C8 oxidative conversion. Inhibition of CYP 3A4 has been shown in vitro but there are no drug interactions described with loperamide as perpetrator. Dimeticone is not absorbed from the gastrointestinal tract.
IPNet drug reports
Uneventful use of this combination preparation is reported in 1 patient with acute porphyria. Also, loperamide in single ingredient preparations is reported to have been used uneventfully by 17 patients.
References
# | Citation details | PMID |
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* | Scientific articles | |
1. | In silico and in vitro screening for inhibition of cytochrome P450 CYP3A4 by comedications commonly used by patients with cancer.
Marechal JD, Yu J, et al. Drug Metab Dispos. 2006 Apr;34(4):534-8. Epub 2006 Jan 13. |
16415122 |
* | Drug reference publications | |
2. | Sweetman SC, editor. Martindale: The complete drug reference. Loperamide hydrochloride. Pharmaceutical Press 2009.
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|
* | Summary of Product Characteristics | |
3. | The electronic Medicines Compendium (emc). Summary of Product Characteristics (SPC). Imodium Classic.
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Netherlands
Imodium Duo · Imodium Duo 2 mg/125 mg, tabletten · LOSIMED DUO · LOSIMED DUO 2 mg/125 mg, tablettenBelgium
Imodium Duo · Imodium Duo 2 mg - 125 mg comp.United Kingdom
Imodium · Imodium Dual Action Relief tablets · Imodium Plus · Imodium Plus caplets · Imodium Plus chewable tabletsDenmark
Imodium Plus · ImolopesimNorway
Imodium CompLuxembourg
IMODIUM DUOFinland
Imodium Plus
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