COLICON SYRUP
DICYCLOVERINE
What it does
Dicycloverine is a medication used to relieve stomach cramps and spasms.
Commonly used for: stomach cramps, abdominal spasms
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Source: Pharmacy and Poisons Board · fetched 2026-01-28 21:56:14 · updated 2026-03-23 04:41:21
Drug Interactions
2Pharmacodynamic Warnings
Dicycloverine appears in TABLE 10: Drugs with antimuscarinic effects
Unknown (2)
Dicycloverine - additive effect
Clozapine can cause constipation, as can dicycloverine; concurrent use might increase the risk of developing com/codemedicalapps/ cal Applications.
Dicycloverine - additive effect
Antipsychotics, second generation (clozapine) can cause constipation, as candicycloverine; concurrent use might increase the risk of developing intestinal obstruction. Also see TABLE 10 p. 1519 Dienog
Data from BNF 85 (British National Formulary). This is not a substitute for professional medical advice. Matched via: exact
About this medicine
Dicycloverine is a medication used to relieve stomach cramps and spasms.
What it treats
- stomach cramps
- abdominal spasms
How it works
Dicycloverine relaxes the muscles in the gut, helping to ease pain and discomfort.
Who it's for
This medicine is for adults and children who experience stomach cramps or spasms.
Cautions
- • Be cautious if you are taking other medications that have antimuscarinic effects, as they may increase side effects.
AI-assisted summary grounded in BNF data - general information only, not medical advice. Always confirm with your pharmacist or doctor.
Clinical monograph: dicycloverine
BNF-referencedDicycloverine, also known as dicyclomine, is an anticholinergic medication primarily used to relieve smooth muscle spasms in the gastrointestinal tract. It is commonly prescribed for conditions such as irritable bowel syndrome (IBS) and other gastrointestinal disorders characterized by spasmodic pain. Dicycloverine works by reducing muscle contractions in the gut, thereby alleviating symptoms associated with abdominal cramping.
Indications
- Irritable bowel syndrome (IBS)
- Gastrointestinal spasm
- Abdominal cramping
Dosage
Children: Refer to the BNF for Children for specific dosing information.
Adults: 20 mg to 40 mg orally, 4 times daily or 10 mg to 20 mg by intramuscular injection, as needed. Do not administer intravenously.
Mechanism of action
Dicyclomine achieves its action partially through direct antimuscarinic activity at the M1, M3, and M2 receptors, and partially through antagonism of bradykinin and histamine. It non-competitively inhibits the action of bradykinin and histamine, leading to a direct relaxant effect on smooth muscle, specifically reducing the strength of contractions observed in ileal spasms. Its major action appears to be a nonspecific direct relaxant effect on smooth muscle rather than competitive antagonism of acetylcholine.
Pharmacodynamics
Dicyclomine is classified as an anticholinergic agent that relaxes the smooth muscles of the intestines. Its duration of action is relatively short, leading to a typical administration schedule of four times daily, with doses ranging from 20-40 mg orally or 10-20 mg via intramuscular injection. It is important to note that dicyclomine should not be administered intravenously.
Pharmacokinetics
Dicyclomine is absorbed through the gastrointestinal tract and metabolized in the liver. The onset of action occurs within 1 hour of administration, with peak effects seen at approximately 1-2 hours. The elimination half-life varies, but it is generally in the range of 1-2 hours, necessitating multiple daily doses to maintain therapeutic levels. The drug is primarily excreted in urine as metabolites.
Contra-indications
- Glaucoma
- Myasthenia gravis
- Severe ulcerative colitis
- Obstructive uropathy
- Obstructive gastrointestinal disease
- Tachyarrhythmias
Adverse effects
- Dizziness
- Dry mouth
- Nausea
- Vomiting
- Constipation
- Blurred vision
- Tachycardia
- Urinary retention
Interactions
- Clozapine (unknown additive effect)
- Second-generation antipsychotics (unknown additive effect)
Precautions
- Use with caution in patients with renal impairment
- Use with caution in patients with hepatic impairment
- Caution in elderly patients due to increased risk of sensitivity to anticholinergic effects
Pregnancy
Dicyclomine is not recommended during pregnancy due to potential risk to the fetus.
Breast-feeding
Dicyclomine is excreted in breast milk and may cause adverse effects in nursing infants; use with caution.
Storage
Store at room temperature, away from light and moisture. Keep out of reach of children.
Formulations
- Oral tablet (20 mg, 40 mg)
- Injection (10 mg, 20 mg)
AI-synthesized from BNF references - general information only, not a substitute for professional medical advice or the current BNF. Verify doses with a pharmacist.
Clinical monograph: Dicycloverinehydrochloride
BNF-referencedDicycloverine hydrochloride, also known as dicyclomine hydrochloride, is an antimuscarinic agent primarily used to relieve symptoms of gastrointestinal disorders marked by smooth muscle spasms. It acts by decreasing gastrointestinal motility and reducing spasms in the smooth muscles of the gut. Dicycloverine is often used in conditions such as irritable bowel syndrome and other gastrointestinal disturbances.
Indications
- Symptomatic relief of gastrointestinal disorders characterized by smooth muscle spasm
- Irritable bowel syndrome
- Acute spasm in diagnostic procedures
Dosage
Children: Child 12–17 years: 10–20 mg three times a day. Child 2–4 years: 5 mg three to four times a day. Child 1 month–1 year: 300–500 micrograms/kg three to four times a day (maximum per dose 5 mg).
Adults: 10–20 mg three times a day, increased if necessary up to 20 mg four times a day; maximum daily dose is 100 mg.
Mechanism of action
Dicycloverine hydrochloride functions as an antimuscarinic by blocking the action of acetylcholine at muscarinic receptors in the smooth muscles of the gastrointestinal tract. This inhibition results in reduced motility and relaxation of the gastrointestinal smooth muscle, alleviating spasms and cramping.
Pharmacodynamics
The primary effect of dicycloverine hydrochloride is the reduction of gut motility due to its antimuscarinic properties. It has a less pronounced antimuscarinic action compared to atropine but may also exhibit some direct relaxant effects on smooth muscle. This dual action helps in relieving abdominal pain associated with smooth muscle spasms.
Pharmacokinetics
Dicycloverine hydrochloride is well absorbed from the gastrointestinal tract. Its onset of action typically occurs within 30 minutes to 1 hour after oral administration, with a duration of effect lasting several hours. The drug undergoes hepatic metabolism and has a variable elimination half-life. Its clearance may be affected by renal function, and caution is advised in patients with renal impairment.
Contra-indications
- Hypersensitivity to dicycloverine or any of its components
- Glaucoma
- Myasthenia gravis
- Severe ulcerative colitis
- Obstructive uropathy
- Severe gastrointestinal obstruction
Adverse effects
- Dry mouth
- Dizziness
- Constipation
- Drowsiness
- Nausea
- Blurred vision
- Urinary retention
- Increased heart rate
- Skin reactions (e.g., flushing, urticaria)
Interactions
- Anticholinergic drugs may enhance effects
- Potentiation of the effects of other CNS depressants such as alcohol
- Antacids containing aluminium may increase risk of toxicity
Precautions
- Use with caution in patients with renal impairment
- May exacerbate conditions like glaucoma and myasthenia gravis
- Monitor for signs of anticholinergic syndrome
Pregnancy
Not known to be harmful; manufacturer advises use only if essential.
Breast-feeding
Avoid; present in milk with potential for causing apnoea in infants.
Storage
Store in a cool, dry place away from direct sunlight. Keep out of reach of children.
Formulations
- Oral solution: Dicycloverine hydrochloride 500 micrograms per 1 ml
- Combination products containing aluminium hydroxide and simeticone
AI-synthesized from BNF references - general information only, not a substitute for professional medical advice or the current BNF. Verify doses with a pharmacist.
Molecular reference: dicycloverine
PubChem CID 3042Molecular formula: C19H35NO2
Mechanism of action
Dicyclomine achieves its action partially through direct antimuscarinic activity of the M1, M3, and M2 receptors; and partially through antagonism of bradykinin and histamine. Dicyclomine non-competitively inhibits the action of bradykinin and histamine, resulting in direct action on the smooth muscle, and decreased strength of contractions seen in spasms of the ileum. ...MAJOR ACTION APPEARS TO BE NONSPECIFIC DIRECT RELAXANT ACTION ON SMOOTH MUSLCE RATHER THAN COMPETITIVE ANTAGONISM OF ACH.
Pharmacodynamics
Dicyclomine is an anticholinergic drug used to relax the smooth muscles of the intestines. It's duration of action is not especially long as it is usually taken 4 times daily with individual doses of 20-40mg orally or 10-20mg by intramuscular injection. Dicyclomine should not be administered intravenously.
Source: PubChem (NCBI) · pathways from PathBank, Reactome, WikiPathways & PharmGKB.
This drug in other countries
The same active ingredient registered across other registries we cover - including different brands.