Open Access Articles- Top Results for Loperamide


Systematic (IUPAC) name
Clinical data
Trade names Imodium and Lopex among others
AHFS/ monograph
MedlinePlus a682280
  • AU: B3
  • US: C (Risk not ruled out)
oral, insufflation
Pharmacokinetic data
Bioavailability 0.3%
Protein binding 97%
Metabolism Hepatic (extensive)
Half-life 7-14 hours
Excretion Faeces (30-40%), urine (1%)
53179-11-6 7pxY
34552-83-5 (with HCl)
A07DA05 (oxide)
PubChem CID 3955
DrugBank DB00836 7pxN
ChemSpider 3818 7pxY
KEGG D08144 7pxY
ChEBI CHEBI:6532 7pxN
Synonyms R-18553
Chemical data
Formula C29H33ClN2O2
477.037 g/mol (513.506 with HCl)
 14pxN (what is this?)  (verify)

Loperamide /lˈpɛrəmd/, a piperidine derivative,[1] is an opioid antimotility drug used against diarrhea resulting from gastroenteritis or inflammatory bowel disease. It was developed by Janssen Pharmaceutica in 1969.

In most countries it is available generically.[2] It is on the World Health Organization's List of Essential Medicines, a list of the most important medication needed in a basic health system.[3]

Medical uses

Loperamide is effective for the treatment of a number of types of diarrhea.[4] This includes control of acute nonspecific diarrhea, mild traveler's diarrhea, irritable bowel syndrome, chronic diarrhea due to bowel resection, and chronic diarrhea secondary to inflammatory bowel disease. It is also useful for reducing ileostomy output. Off Label uses for loperamide also include chemotherapy induced diarrhea, especially related to irinotecan use.

Loperamide should not be used as the primary treatment in cases of bloody diarrhea, acute exacerbation of ulcerative colitis, or bacterial enterocolitis.[5]

Loperamide is often compared to diphenoxylate. Recent studies suggest that loperamide is more effective and has lower neural side effects.[6][7][8]

Side effects

Treatment should be avoided in the presence of high fever or if the stool is bloody (dysentery). Treatment is not recommended for patients that could suffer detrimental effects from rebound constipation. If there is a suspicion of diarrhea associated with organisms that can penetrate the intestinal walls, such as E. coli O157:H7 or salmonella, loperamide is contraindicated as a primary treatment.[5] Loperamide treatment is not used in symptomatic C. difficile infections, as it increases the risk of toxin retention and precipitation of toxic megacolon.

Loperamide should be administered with caution to patients suffering from hepatic impairment due to reduced first pass metabolism.[9] Additionally, caution should be used when treating patients with advanced HIV as there have been cases of both viral and bacterial toxic megacolon. If abdominal distension is noted, therapy with loperamide should be discontinued.[10]

The use of loperamide in children under 2 years is not recommended. There have been rare reports of fatal paralytic ileus associated with abdominal distention. Most of these reports occurred in the setting of acute dysentery, overdose, and with very young children less than two years of age.[11] A systematic review and meta-analysis examined control trials of loperamide in children under 12 years old, and found that serious adverse events occurred only in children under 3 years old. The study reported that the use of loperamide should be contraindicated in children under 3 years old, systemically ill, malnourished, moderately dehydrated, or have bloody diarrhea.[12] In 1990, all pediatric formulations of the antidiarrheal loperamide were banned in Pakistan.[13]

Loperamide is not recommended in the UK for use during pregnancy nor by nursing mothers.[14] In the US, loperamide is classified by the FDA as pregnancy category C. Studies in rat models have shown no teratogenicity, but there have not been sufficient studies in humans.[15] One controlled, prospective study of 89 women exposed to loperamide during the first trimester showed no increased risk of malformations. This, however, was only one study with a small sample size.[16] Loperamide can be present in breast milk, and is not recommended for breast feeding mothers.[10]

Adverse drug reactions (ADRs) most commonly associated with loperamide are constipation (which occurs in 1.7%-5.3% of users), dizziness (up to 1.4%), nausea (0.7%-3.2%), and abdominal cramps (0.5%-3.0%).[17] Rare, but more serious, side-effects include: toxic megacolon, paralytic ileus, angioedema, anaphylaxis/allergic reactions, toxic epidermal necrolysis, Stevens-Johnson syndrome, erythema multiforme, urinary retention, and heat stroke.[18] The most frequent symptoms of loperamide overdose are drowsiness, vomiting and abdominal pain or burning.[19]

Drug interactions

Loperamide is a substrate of P-glycoprotein, therefore the concentration of Loperamide will increase when given with a P-Glycoprotein inhibitor.[17] Common P-Glycoprotein inhibitors include quinidine, ritonavir, and ketoconazole, among others.[20] Loperamide is also capable of decreasing the concentration of other P-Glycoprotein substrates. As an example, when saquinavir concentrations can decrease by half when given with loperamide.[17]

Loperamide is an anti-diarrheal agent which decreases intestinal movement. As such, when combined with other antimotility drugs, there is an increased risk of constipation. These drugs include, but are not limited to, other opioids, antihistamines, antipsychotics, and anticholinergics.[21]

Mechanism of action

File:Loperamide ball-and-stick.png
Ball-and-stick model of loperamide molecule

Loperamide is an opioid-receptor agonist and acts on the μ-opioid receptors in the myenteric plexus of the large intestine; by itself it does not affect the central nervous system. It works similarly to morphine, by decreasing the activity of the myenteric plexus, which in turn decreases the tone of the longitudinal and circular smooth muscles of the intestinal wall.[22][23] This increases the amount of time substances stay in the intestine, allowing for more water to be absorbed out of the fecal matter. Loperamide also decreases colonic mass movements and suppresses the gastrocolic reflex.[24]

Ability to cross the blood–brain barrier

Loperamide does not cross the blood–brain barrier because it is subject to efflux by P-glycoprotein. This mechanism effectively shields the CNS from exposure (and thus risk of CNS tolerance/dependence) to loperamide.[25]

Concurrent administration of P-glycoprotein inhibitors such as quinidine could potentially allow loperamide to cross the blood–brain barrier. Quinidine with loperamide was found to produce respiratory depression, indicative of central opioid action.[26]

Loperamide has been shown to cause a mild physical dependence during preclinical studies, specifically in mice, rats, and rhesus monkeys. Symptoms of mild opiate withdrawal were observed following abrupt discontinuation of long-term treatment of animals with loperamide.[27][28]

When originally approved for medical use in the United States, loperamide was considered a narcotic and was put into Schedule II of the Controlled Substances Act 1970. It was transferred to Schedule V on 17 July 1977 and then decontrolled as of 3 November 1982. (source: Federal Register)


Loperamide hydrochloride was first synthesized by Paul Janssen from Janssen Pharmaceutica in Beerse (Belgium), following previous discoveries of diphenoxylate hydrochloride (1956) and fentanyl citrate (1960).[29]

The first clinical on loperamide were published in 1973 in the Journal of Medicinal Chemistry[2] with the inventor being one of the authors.

The trial against placebo was conducted from December 1972 to February 1974, its results being published in 1977 in Gut journal, an edition of British Society of Gastroenterology.[30]

The drug was patented in the USA in 1973.[31][32]

In 1973 Janssen started to promote loperamide under the brand name Imodium.

In December 1976 Imodium got FDA approval.[33]

During the 1980s, Imodium became the best-selling prescription antidiarrheal in the United States.[34]

In March 1988 McNeil Pharmaceutical began selling loperamide as the OTC product under the brand name Imodium A-D.[35]

In the 1980s there also existed loperamide in the form of drops (Imodium Drops) and syrup. Initially it was intended for children's usage, but Johnson & Johnson voluntarily withdrew it from the market in 1990 after 18 cases of paralytic ileus (resulting in 6 deaths) has been registered in Pakistan and reported by World Health Organization.[36] In the following years (1990-1991) products containing loperamide have been restricted for children use in a number of countries (ranging from 2 to 5 years of age).[37]

In the late 1980s prior to the expiration of US Patent in January 30, 1990,[34] McNeil company started to develop Imodium Advanced containing loperamide and simethicone for treating both diarrhea and flatulence. In March 1997 the company patented such combination.[38] The drug has been approved in June 1997 by FDA as Imodium Multi-Symptom Relief in the form of a chewable tablet.[39]

In November 1993 loperamide has been launched as an orally disintegrating tablet based on Zydis technology.[40][41] Imodium Instant Melts from Johnson & Johnson is currently the only loperamide available in the form of orally disintegrating tablets.[42][43]

In 2013 loperamide in the form of 2 mg tablets has been added to WHO Model List of Essential Medicines.[44]


File:Loperamide synthesis.png
Loperamide synthesis:[45] P. Janssen, C. Niemegeers, U.S. Patent 3,714,159 (1973), U.S. Patent 3,884,916 (1975).

See also

Brand names

Lopex, Imodium, Dimor, Fortasec, Lopedium, Gastro-Stop, Pepto Diarrhea Control, Lopamide.


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External links