Beemine
Beemine Uses, Dosage, Side Effects, Food Interaction and all others data.
Beemine is a parasympathomimetic, specifically, a reversible cholinesterase inhibitor. By interfering with the breakdown of acetylcholine, Beemine indirectly stimulates both nicotinic and muscarinic receptors. It does cross the blood-brain barrier but only poorly. Beemine binds to the anionic site of cholinesterase. The drug blocks the active site of acetylcholinesterase; so the enzyme can no longer break down the acetylcholine molecules before they reach the postsynaptic membrane receptors. This allows for the threshold to be reached so a new impulse can be triggered in the next neuron. In myasthenia gravis there are too few acetylcholine receptors. So with the acetylcholinesterase blocked, acetylcholine can bind to the few receptors and trigger a muscular contraction.
Beemine is a cholinesterase inhibitor used in the treatment of myasthenia gravis and to reverse the effects of muscle relaxants such as gallamine and tubocurarine. Beemine, unlike physostigmine, does not cross the blood-brain barrier. By inhibiting acetylcholinesterase, more acetylcholine is available in the synapse, therefore, more of it can bind to the fewer receptors present in myasthenia gravis and can better trigger muscular contraction.
Trade Name | Beemine |
Availability | Prescription only |
Generic | Neostigmine |
Neostigmine Other Names | Eustigmin, Eustigmine, Neostigmina |
Related Drugs | pyridostigmine, bethanechol, Mestinon, Soliris, Vyvgart, Ultomiris, sugammadex, Urecholine, eculizumab, Bridion |
Type | Injection |
Formula | C12H19N2O2 |
Weight | Average: 223.2915 Monoisotopic: 223.144652862 |
Protein binding | Protein binding to human serum albumin ranges from 15 to 25 percent. |
Groups | Approved, Vet approved |
Therapeutic Class | Anti-cholinesterases, Drugs used in Myasthenia Gravis |
Manufacturer | Biomiicron Pharmaceuticals |
Available Country | India |
Last Updated: | September 19, 2023 at 7:00 am |
Uses
Beemine Methyl Sulphate is used for-
- Reversal of nondepolarising neuromuscular blockade for surgical anesthetic procedures
- The prevention and treatment of post-operative abdominal distention and urinary retention after mechanical obstruction has been excluded.
- Treatment of the systemic control of Myasthenia Gravis when oral therapy is impractical.
Beemine is also used to associated treatment for these conditions: Curarization therapy, Myasthenia Gravis, Neuromuscular Blockade, Ogilvie's syndrome, Postoperative Urinary Retention, Post-operative intestinal atony
How Beemine works
Beemine is a parasympathomimetic, specifically, a reversible cholinesterase inhibitor. The drug inhibits acetylcholinesterase which is responsible for the degredation of acetylcholine. So, with acetylcholinesterase inhibited, more acetylcholine is present By interfering with the breakdown of acetylcholine, neostigmine indirectly stimulates both nicotinic and muscarinic receptors which are involved in muscle contraction.. It does not cross the blood-brain barrier.
Dosage
Beemine dosage
Reversal of the effects of Non-depolarizing Neurormuscular Blocking Agents: The usual dose is 0.5 to 2 mg given by slow intravenous injection over 60 seconds; repeated as required. Total dose should not exceed 5 mg (in exceptional cases). When Beemine is administered intravenously, it is recommended that Atropine Sulphate (0.6-1.2 mg) also be given intravenously using separate syringe.
Prevention of post-operative abdominal distention and urinary retention: 0.25 mg intramuscularly or subcutaneously as soon as possible after operation; repeat every 4 6 hours for 2-3 days.
Treatment of post-operative abdominal distention: 0.5 mg intramuscularly or subcutaneously or as required.
Treatment of urinary retention: 0.5 mg intramuscularly or subcutaneously. If urination does not occur within an hour, the patient should be catheterized. After the patient has voided, or the bladder has been emptied, continue the 0.5 mg injection every 3 hours, for at least 5 injections.
Symptomatic control of Myasthenia Gravis: 0.5 mg intramuscularly or subcutaneously. Subsequent dose should be based on the individual patient's response.
Neonates: 50-250 micrograms (0.1 to 0.5 ml) every 4 hours.
Children: 200-500 micrograms (0.4 ml to 1 ml) as recommended.
Side Effects
Nausea, vomiting, increased salivation, diarrhoea and abdominal cramps (more marked with high doses). Signs of overdose are increased gastrointestinal discomfort, bronchial secretions and sweating, involuntary defecation and micturition, miosis, nystagmus, bradycardia, hypotension, agitation, excessive dreaming and weakness eventually leading to fasciculation and paralysis.
Toxicity
Overdosage of Beemine can cause cholinergic crisis, which is characterized by increasing muscle weakness, and through involvement of the muscles of respiration, may result in death. The LD 50 of neostigmine methylsulfate in mice is 0.3 ± 0.02 mg/kg intravenously, 0.54 ± 0.03 mg/kg subcutaneously, and 0.395 ± 0.025 mg/kg intramuscularly; in rats the LD 50 is 0.315 ± 0.019 mg/kg intravenously, 0.445 ± 0.032 mg/kg subcutaneously, and 0.423 ± 0.032 mg/kg intramuscularly.
Precaution
Asthma, bradycardia, recent myocardial infarction, epilepsy, hypotension, parkinsonism, vagotonia, peptic ulceration. Atropine or other antidote to muscarinic effccts may be necessary (particularly when Beemine is given by injection), but it should not be given routinely as it may mask signs of overdose.
Interaction
Anti-arrhythmic Procainamide, Quinidine and possibly Propafenone antagonise effect of Beemine. Antibacterials, Aminoglycosides, Clindamycin, Lincomycin and Polymyxins antagonise effect of Beemine.
Food Interaction
No interactions found.Beemine Drug Interaction
Moderate: pyridostigmineUnknown: aspirin, epinephrine, RHO Immunoglobulin , calcium / vitamin d, Allergy , glucose, heparin, ipratropium, acetaminophen, procaine penicillin, phenytoin, valproic acid, multivitamin, thiamine, cyanocobalamin, pyridoxine, ascorbic acid, phytonadione, phytonadione
Beemine Disease Interaction
Major: bradycardia, bronchospasm, coronary artery disease, parkinsonism, PUD, seizuresModerate: hyperthyroidism
Elimination Route
Beemine bromide is poorly absorbed from the gastrointestinal tract following oral administration
Half Life
The half-life ranged from 42 to 60 minutes with a mean half-life of 52 minutes.
Pregnancy & Breastfeeding use
Pregnancy Category C. There are no adequate or well-controlled studies of Beemine in either laboratory animals or in pregnantwomen. It is not known whether Beemine can cause fetal harm when administered to a pregnant woman or can affect reproductive capacity. Beemine should be given to a pregnant woman only if clearly needed.
Nonteratogenic Effects: Anticholinesterase drugs may cause uterine irritability and induce premature labor when given intravenously to pregnant women near term.
Nursing Mothers: It is not known whether Beemine is excreted in human milk. Because many drugs are excreted in human milk and because of the potential for serious adverse reactions from Beemine in nursing infants, a decision should be made whether to discontinue nursing or to discontinue the drug, taking into account the importance of the drug to the mother.
Contraindication
Beemine is contraindicated in patients with known hypersensitivity to the drug. It is also contraindicated in patients with peritonitis or mechanical obstruction of the intestinal or urinary tract.
Storage Condition
Store in a cool and dry place, protected from light.
Innovators Monograph
You find simplified version here Beemine
Beemine contains Neostigmine see full prescribing information from innovator Beemine Monograph, Beemine MSDS, Beemine FDA label