Buscolysin

Quick links to important sections

Buscolysin

Medically reviewed

Marina Burgos

Last updated on 10/01/2026

This page provides general, reference-level information compiled from official medical sources. It is not a substitute for professional medical advice, diagnosis, or treatment. For decisions about your health, please consult a qualified healthcare professional.

Overview of Buscolysin

Property Description
Active Ingredient Hyoscine Butylbromide (Scopolamine Butylbromide)
Form Tablets and Injectable Solution
Pharmacological Class Antispasmodic, Anticholinergic (Antimuscarinic)
Common Use Alleviating pain caused by muscle spasms in the abdomen
Origin Semisynthetic derivative of hyoscine

What Type of Medicine is Buscolysin?

Buscolysin is a commercial name for the medicinal product containing the active ingredient, Hyoscine Butylbromide, which is classified primarily as an antispasmodic agent. This pharmacological class, recognized as a parasympatholytic or anticholinergic agent, functions specifically by interrupting nerve signals that cause involuntary muscle contractions, or spasms. The active substance is defined as a single-ingredient medicine and is derived as a semisynthetic compound of the naturally occurring alkaloid hyoscine (scopolamine). Its established efficacy in treating abdominal spasm and pain is widely recognized in clinical practice.


Forms and Unique Characteristics of Hyoscine Butylbromide

Buscolysin is commonly available in oral tablets and as an injectable solution for parenteral administration. The active substance is chemically unique as a quaternary ammonium compound. This structural feature is crucial because it limits the substance's ability to penetrate the blood-brain barrier. Consequently, its therapeutic action is highly targeted and peripheral, focusing the effect primarily on the smooth muscles of the digestive and genitourinary tracts while minimizing potential influence on the central nervous system.


General Purpose of an Antispasmodic Agent

The general purpose of the medicine is to achieve localized smooth muscle relaxation to alleviate the general discomfort and pain associated with spasms. It acts as a chemical signal blocker, preventing the neurotransmitter acetylcholine from initiating the involuntary, forceful tightening of muscles in the abdominal organs. This intervention directly addresses the physiological cause of the spasm, offering effective relief from the cramping pain, such as that experienced during episodes of irritable bowel syndrome discomfort.

What side effects are possible with Buscolysin?

Possible Side Effects and Safety Information

The safety profile of Buscolysin (Hyoscine Butylbromide) is largely characterized by its anticholinergic class of effects, which result from the interruption of nerve signals. The documented undesirable effects and safety constraints are strictly based on government regulatory standards.


Officially Documented Adverse Reactions

Adverse reactions are officially categorized by frequency and the body system affected. Many effects are related to the gastrointestinal and cardiovascular systems.

  • Common Reactions (for the injectable form) include tachycardia (fast heart rate), dry mouth, and accommodation disorders (difficulty with eye focusing). Constipation is also reported as a common effect for the injection, and dry mouth is uncommon for the tablets.
  • Rare Reactions include urinary retention (primarily with the tablet form).

Reactions whose frequency cannot be estimated (Not Known) from available data include serious events like anaphylactic shock and other severe hypersensitivity reactions.


Serious Safety Considerations

Regulatory documents emphasize the risk of serious adverse reactions, which, while categorized as having a not known frequency, include anaphylactic shock and severe cardiac events, such as cardiac arrest and acute myocardial infarction. These risks are particularly noted with the injectable solution in patients with pre-existing cardiovascular disease.


Population-Specific Safety Constraints

The medicine is officially subject to restrictions and warnings for specific groups. Caution is advised for individuals susceptible to anticholinergic complications, such as those predisposed to narrow-angle glaucoma or conditions leading to urinary or intestinal obstruction. Furthermore, the drug is generally not recommended for use during pregnancy or lactation due to insufficient data to definitively exclude a risk.

Overdose and Emergency Response

Overdose and when to seek help

The official regulatory documents define the overdose profile of Hyoscine Butylbromide (Buscolysin) as an exaggeration of its established anticholinergic effects, classifying the presentation by specific clinical signs and required emergency actions.

Documented Overdose Presentations

Domain Official Regulatory Statement
Clinical Manifestations The overdose presentation is characterized by exaggerated anticholinergic symptoms, including tachycardia (fast heart rate), urinary retention, dry mouth, reddening of the skin (flushing), and transient visual disturbances (accommodation disorders). Inhibition of gastrointestinal motility and drowsiness may also occur.
Severe Outcomes Cheynes-Stokes respiration has been reported in overdosage cases. While serious signs of poisoning have generally not been observed in man, the possibility of respiratory paralysis and the occurrence of psychiatric disorders (e.g., confusion) cannot be totally ruled out.
Management Procedures Symptoms of overdosage respond to parasympathomimetics. Procedural management measures cited include gastric lavage with activated charcoal for oral poisoning, catheterisation for urinary retention, and intubation for respiratory paralysis. Pilocarpine is specified for local administration in patients with glaucoma-related complications.

When Immediate Medical Help is Required

Regulatory authorities require that immediate medical attention be sought upon the first signs of suspected overdosage. This instruction applies to all potential manifestations. Urgent ophthalmological advice must also be sought if the patient develops a painful, red eye accompanied by loss of vision.

Therapeutic Uses of Buscolysin

What Buscolysin Treats: Main Uses and Benefits

Buscolysin (Hyoscine Butylbromide) is applied across domains where additional symptomatic support is needed, and is used for managing symptoms related to physical discomfort in the abdominal and pelvic regions. It is relevant across domains involving heightened symptom expression, and is considered relevant for acute spasm and its role in diagnostic procedures.


Key Therapeutic Applications

The medication is commonly used across conditions presenting with episodic or fluctuating symptom patterns. It is relevant for managing symptoms associated with specific conditions, including Irritable Bowel Syndrome (IBS) flare-ups, renal colic, biliary colic, and dysmenorrhea. The key therapeutic benefit provides support that contributes to easing the overall symptom load of these visceral cramps. In clinical settings, its properties are applied in scenarios where symptom management is required before procedures like endoscopy or pyelography. This assists with maintaining functional stability during episodes of discomfort.


Quick Fact

Quick Fact: Relief for Spasmodic Pain

This medication is generally considered relevant for symptoms that interfere with daily functioning when the pain is related to symptoms of increased muscular activity in the gastrointestinal or genitourinary tracts.

Eligibility and Restrictions for Use

Who Can and Cannot Use Buscolysin?

Buscolysin (Hyoscine Butylbromide) use is governed by specific eligibility rules established in official regulatory labeling to ensure patient safety and appropriate use.


Absolute Contraindications (Must Not Use)

The medicine is formally contraindicated and must not be used by patients with:

  • Myasthenia Gravis
  • Narrow-Angle Glaucoma
  • Mechanical Stenosis or Obstructive Ileus of the gastrointestinal tract
  • Megacolon
  • Hypersensitivity to the active ingredient or excipients

Age-Related and Lifecycle Restrictions

Population Eligibility Status (Regulatory Guidance)
Adults and Adolescents Approved for standard use.
Children Under 6 Years (Oral Tablets) Not recommended due to insufficient data on safety and efficacy.
Pregnant Women Not recommended as a precautionary measure due to limited human data.
Breastfeeding Women Not recommended due to insufficient information on excretion into milk.

Use Requiring Special Caution

Caution is required in patients susceptible to urinary or intestinal obstruction (e.g., due to prostatic enlargement) and in patients prone to tachycardia or other severe heart conditions, as the drug may exacerbate these issues.

What should I know about interactions with other medicines?

Interactions with other medicines and products

Official regulatory documents define the interaction profile of Hyoscine Butylbromide primarily through pharmacodynamic effects and altered absorption patterns. The medicine's anticholinergic classification means co-administration with other anticholinergic agents (such as tricyclic antidepressants, antihistamines, or certain antipsychotics) may lead to an intensification of the parasympatholytic effect.

Conversely, concomitant use with dopamine antagonists (e.g., metoclopramide or domperidone) can result in a diminution of the gastrointestinal effects of both substances, as their actions on gut motility counteract each other. Furthermore, the chronotropic action of beta-adrenergic substances may be enhanced.

Administration restrictions apply to the injectable form: co-administration with anticoagulant drugs is contraindicated for the intramuscular injection route due to the official risk of intramuscular haematoma. For the oral formulation, antacids and adsorbent anti-diarrheals lower the absorption of the active ingredient and require a mandatory timing separation, as they must be taken at least one hour before Hyoscine Butylbromide. In regulatory documents, alcohol is noted to increase the chance of side effects such as drowsiness.

Mechanism of Action

The core mechanism involves the drug acting as a competitive antagonist at the muscarinic acetylcholine receptors ( mAChRs), particularly the M3 subtype, located on smooth muscle cells. This interaction directly blocks the body's neurotransmitter, acetylcholine (ACh), from binding and triggering the signal required for muscle contraction. The resulting molecular cascade prevents the mobilization of Ca^2+ ions inside the muscle fiber, resulting in the physiological consequence of reduced involuntary muscle tone and contraction. The molecule's unique quaternary ammonium structure is a defining feature of its mechanism, as it imparts a high polarity that restricts the drug's ability to cross the blood-brain barrier. This structural constraint ensures the anticholinergic mechanism is highly localized and concentrated on the peripheral receptors of the visceral smooth muscle in the abdomen and pelvis. The mechanism provides highly focused modulation of cholinergically-mediated smooth muscle signaling but is physiologically constrained and does not modulate signaling unrelated to active muscle contraction or processes caused by fixed, structural limitations, such as a physical mechanical obstruction

Dosage and Administration Information

How to Use Buscolysin: Administration Guidelines

Buscolysin, which contains Hyoscine Butylbromide, is used according to specific administration guidelines. The guidelines differ based on the dosage form, which includes oral tablets and an injectable solution (for intravenous, intramuscular, or subcutaneous delivery).


Administration Details and Dosage Regimens

The choice of route is typically determined by the clinical scenario, with the injection form reserved for acute spasm or use during diagnostic procedures.

Administration Route Standard Adult Dose Frequency and Timing
Oral Tablets (10 mg) 10 mg to 20 mg per dose Up to three to five times daily
Parenteral Injection 20 mg (single dose) May be repeated after thirty minutes if required; maximum 100 mg total daily dose

Special Conditions for Oral Use: Tablets must be swallowed whole with adequate water; they should not be crushed or chewed. The medicine is generally not intended for continuous daily use over extended periods without investigation into the cause of spasm.


Procedural and Population Rules

Injection Requirements: Intravenous injection must be administered slowly to comply with administration protocols, and the injectable solution is intended for single use only, with any remaining contents to be discarded. The solution may be diluted with glucose or sodium chloride 0.9% for infusion.

Age-Specific Rules: Oral tablets are not recommended for children under the age of six. For children aged 6 to 12 years, the dose is typically 10 mg, up to three times per day.

Recent Clinical Evidence

Research Evidence / Overview of Studies for Buscolysin


Evidence for use in Spasmodic Abdominal Pain

Buscolysin (hyoscine butylbromide) has been studied extensively in research involving individuals experiencing abdominal pain associated with cramps or spasms in the gastrointestinal, biliary, and urinary tracts. Research includes multiple short-term, placebo-controlled clinical trials, where the primary focus was to examine changes in abdominal discomfort and symptom severity. Studies monitored patient-reported outcomes related to physical discomfort and acute pain episodes.

In these controlled research settings, findings indicate patterns of change in discomfort levels in the observed populations during the study period. The evidence contributes to understanding symptom patterns observed during acute episodes. However, the available data are focused on the short-term management of these episodic symptoms.


Evidence in Diagnostic Procedures

Research has explored the use of Buscolysin to reduce smooth muscle movement during various medical imaging procedures, such as MRI or radiological studies of the gastrointestinal and urinary tracts. These studies primarily monitored changes in internal smooth muscle motility and the resulting quality of the diagnostic images. The evidence suggests that reducing muscle motion during these specific diagnostic scenarios was observed in the populations studied.


Long-term Data and Special Populations

Buscolysin research primarily involves short-term administration for acute symptom relief or single-use diagnostic support; therefore, follow-up durations were limited across the core evidence base. There is limited information for long-term outcomes regarding the sustained, daily use of the drug. Research has included some special populations, such as older adults; however, data for certain groups remain insufficient, including evidence for use in pregnant women or children, as these groups pose specific research considerations.

Key Studies & References

  1. A Comprehensive Review of the Effects of Hyoscine Butylbromide in Childhood
  2. Public Assessment Report Pharmacy to General Sales List Reclassification Buscopan IBS Relief Hyoscine Butylbromide 10mg
  3. Hyoscine N-Butylbromide 20mg/mL Solution for Injection (I.M./I.V.) - Philippine FDA Drug Label

Frequently Asked Questions (FAQ)

Common questions about Buscolysin (FAQ)

Q: What is Buscolysin used for?

A: Buscolysin is indicated for the treatment of pain associated with spasms of the digestive tract, biliary tract, and urinary tract. It is typically prescribed to relieve cramps and discomfort related to these conditions.

Q: How does Buscolysin work?

A: Buscolysin belongs to a class of medications called antispasmodics. It is believed to work by relaxing the muscles in the walls of the stomach, intestines, and urinary tract, which helps to ease the painful spasms.

Q: What are the common side effects of Buscolysin?

A: As with most medications, Buscolysin may be associated with side effects. Common side effects that may be listed on the product labeling include dry mouth, blurred vision, dizziness, and fast heartbeat (tachycardia). If you experience any severe or concerning effects, contact your healthcare provider immediately.

Q: Can I take Buscolysin with other medications?

A: Buscolysin may interact with other medications, including prescription and over-the-counter products, as well as herbal supplements. It is important to provide your healthcare provider and pharmacist with a complete list of all products you currently use so they can check for potential interactions and ensure your safety.

Q: What should I do if I miss a dose?

A: Guidance for a missed dose is typically found in the product information leaflet or provided by your prescribing healthcare professional. In general, if a dose is missed, it is often advised to take it as soon as you remember unless it is almost time for your next scheduled dose. Do not take a double dose to make up for a missed one. Always consult your doctor or pharmacist for specific instructions regarding your treatment schedule.

How should Buscolysin be stored and disposed of?

How to Store and Dispose of Buscolysin?

The storage and disposal of Buscolysin (Hyoscine Butylbromide) must strictly follow the conditions specified in official regulatory documents to maintain product stability and safety.

Official Storage Conditions

Requirement Specification
Temperature Store below 25 C or 30 C, depending on the specific product label.
Environmental Keep the medicine in a dry place and store in the original package to protect from light.
Handling Do not freeze. The product should not be used after the expiry date printed on the packaging.
Safety Rule Must be kept out of the sight and reach of children.

Disposal Instructions

Unused or expired Buscolysin must be disposed of in accordance with local requirements. Regulatory guidelines prohibit throwing away medicines via wastewater or household waste to protect the environment.

Attention! Always consult to a doctor or pharmacist before using pills or medicines.

Available in countries:

Equivalent of Buscolysin found in:

A-Z Index: