Ubretid (Tablets, Solution) Instructions for Use
ATC Code
N07AA03 (Distigmine bromide)
Active Substance
Distigmine bromide (Rec.INN registered by WHO)
Clinical-Pharmacological Group
Cholinesterase inhibitor
Pharmacotherapeutic Group
Anticholinesterase agent
Pharmacological Action
Inhibitor of acetylcholinesterase and pseudocholinesterase. It has an indirect cholinomimetic effect due to reversible inhibition of cholinesterase and potentiation of the action of endogenous acetylcholine.
It improves neuromuscular transmission, enhances the tone and motility of the gastrointestinal tract, increases the tone of the bladder, bronchi, and the secretion of exocrine glands.
It causes bradycardia and lowers blood pressure. It constricts the pupil, lowers intraocular pressure, and causes spasm of accommodation.
Being a quaternary ammonium compound, Distigmine bromide penetrates poorly through cell membranes, does not cross the blood-brain barrier and does not affect the neurotransmitter acetylcholine in the central nervous system.
It also does not have a significant effect on impulse transmission in the ganglia of the autonomic nervous system. It has a longer duration of action than neostigmine.
Pharmacokinetics
After oral administration, it is metabolized by hydrolysis. It does not cross the blood-brain barrier. Metabolites are excreted in the urine.
Indications
Prevention and treatment of postoperative intestinal atony and paralytic ileus; atony of the bladder and ureters, functional insufficiency of the bladder sphincter, hypotension of the bladder; atonic and hypotonic constipation, megacolon; peripheral paralysis of striated muscles; myasthenia gravis.
ICD codes
| ICD-10 code | Indication |
| G70 | Myasthenia gravis and other disorders of the neuromuscular junction |
| G83.9 | Paralytic syndrome, unspecified |
| K56 | Paralytic ileus and intestinal obstruction without hernia |
| K59.0 | Constipation |
| K59.3 | Megacolon, not elsewhere classified |
| K59.8 | Other specified functional intestinal disorders |
| N31.2 | Neurogenic bladder weakness, not elsewhere classified |
| ICD-11 code | Indication |
| 8C6Z | Myasthenia gravis or other specified diseases of the neuromuscular junction, unspecified |
| DA91.Z | Unspecified obstruction of small intestine |
| DB30.Z | Unspecified obstruction of large intestine |
| DB32.1 | Slow-transit constipation |
| DB32.20 | Toxic megacolon |
| DB32.2Z | Megacolon, unspecified |
| DB32.3 | Acquired hypoganglionosis of the colon |
| DB32.Z | Colonic motility disorders, unspecified |
| DD90.2 | Functional heartburn |
| DD91.1 | Functional constipation |
| DD91.Y | Other specified irritable bowel syndrome or functional bowel disorders |
| DD93.Y | Other specified functional gastrointestinal disorders in infants, toddlers and school-age children |
| DE2Z | Diseases of the digestive system, unspecified |
| GC01.4 | Neuromuscular dysfunction of the bladder, not elsewhere classified |
| MB5Z | Paralytic symptoms, unspecified |
Dosage Regimen
| The method of application and dosage regimen for a specific drug depend on its form of release and other factors. The optimal dosage regimen is determined by the doctor. It is necessary to strictly adhere to the compliance of the dosage form of a specific drug with the indications for use and dosage regimen. |
Administer Ubretid orally or by intramuscular injection. Select the route and dosage based on the specific medical indication and individual patient response.
For oral administration, take 5 mg to 10 mg once daily. The tablet should be swallowed whole with a sufficient amount of water, typically in the morning before breakfast.
For intramuscular injection, administer 500 micrograms (0.5 mg) once daily. Inject deeply into a large muscle mass, observing strict aseptic technique.
Adjust the duration of therapy individually. Continue treatment until the desired therapeutic effect is achieved, such as restoration of normal bladder or intestinal function. Do not exceed the recommended daily dose.
In cases of postoperative atony, initiate therapy as soon as clinically indicated after surgery. For chronic conditions like myasthenia gravis, use as part of a long-term management plan under strict medical supervision.
Monitor for signs of cholinergic excess, particularly with long-term use. Reduce the dosage or discontinue treatment if adverse reactions such as severe bradycardia, excessive salivation, or muscle twitching occur.
Adverse Reactions
From the cardiovascular system bradycardia.
From the digestive system nausea, vomiting, diarrhea, spasmodic abdominal pain, increased salivation.
Other twitching of the tongue muscles and skeletal muscles.
Contraindications
Hypersensitivity to distigmine bromide and to bromine; hypervagotonia, intestinal hypertonus, marked arterial hypotension, chronic heart failure, recent myocardial infarction, thyrotoxicosis, iritis, bronchial asthma, myotonia, tetany, epilepsy, Parkinson’s disease, postoperative and hemodynamic shock.
Use in Pregnancy and Lactation
During pregnancy and breastfeeding, it should be used only after consultation with a doctor, in cases where the intended benefit to the mother outweighs the potential risk to the fetus or infant.
Special Precautions
Use with caution in bradycardia, arrhythmia, arterial hypotension, Addison’s disease, hyperthyroidism, gastric and duodenal ulcer.
In cases of temporary functional amenorrhea, Distigmine bromide may cause menstrual-like bleeding.
Effect on ability to drive vehicles and operate machinery
During treatment, one should refrain from driving vehicles and other potentially hazardous activities that require rapid psychomotor reactions.
Drug Interactions
With simultaneous use with m-cholinoblockers, psychotropic agents, antihistamines, peripheral muscle relaxants, corticosteroids, antiarrhythmic agents, aminoglycosides, the clinical efficacy of distigmine bromide is reduced.
Storage Conditions
Store at 2°C (36°F) to 25°C (77°F). Keep in original packaging, protected from light. Keep out of reach of children.
Dispensing Status
Rx Only
Important Safety Information
This information is for educational purposes only and does not replace professional medical advice. Always consult your doctor before use. Dosage and side effects may vary. Use only as prescribed.
Medical DisclaimerBrand (or Active Substance), Marketing Authorisation Holder, Dosage Form
Tablets 5 mg: 20 pcs.
Marketing Authorization Holder
Nycomed Austria, GmbH (Austria)
Dosage Form
| Ubretid | Tablets 5 mg: 20 pcs. |
Dosage Form, Packaging, and Composition
| Tablets | 1 tab. |
| Distigmine bromide | 5 mg |
10 pcs. – blisters (2) – cardboard packs.
Injection solution 500 mcg/1 ml: amp. 5 pcs.
Marketing Authorization Holder
Nycomed Austria, GmbH (Austria)
Dosage Form
| Ubretid | Injection solution 500 mcg/1 ml: amp. 5 pcs. |
Dosage Form, Packaging, and Composition
| Injection solution | 1 ml |
| Distigmine bromide | 500 mcg |
1 ml – ampoules (5) – cardboard packs.
