Neostigmine methylsulfate
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Gloria Picoy [2]
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Overview
Neostigmine methylsulfate is a cholinesterase Inhibitor that is FDA approved for the treatment of symptomatic control of myasthenia gravis, prevention of postoperative distention and urinary retention, treatment of postoperative distention, treatment of urinary retention, reversal effects of non-depolarizing blocking agents.. Common adverse reactions include hypotension, nausea and vomiting.
Adult Indications and Dosage
FDA-Labeled Indications and Dosage (Adult)
Symptomatic control of myasthenia gravis
- Dosage: 1 mL of the 1:2000 solution (0.5 mg) subcutaneously or intramuscularly.
- Subsequent doses should be based on the individual patient's response.
- In most patients, however, oral treatment with Neostigmine Bromide tablets, 15 mg each, is adequate for control of symptoms.
Prevention of postoperative distention and urinary retention
- Dosage: 0.25 mg subcutaneously or intramuscularly as soon as possible after operation
- Repeat every 4 to 6 hours for two or three days.
Treatment of postoperative distention
- Dosage: 1 mL of the 1:2000 solution (0.5 mg) subcutaneously or intramuscularly, as required.
Treatment of urinary retention
- Dosage: 1 mL of the 1:2000 solution (0.5 mg) subcutaneously or intramuscularly.
- 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 injections every three hours for at least 5 injections.
Reversal Effects of Non-depolarizing Blocking Agents
- Dosage: 0.5 to 2 mg Neostigmine Methylsulfate Injection given by slow intravenous injection, repeated as required.
- When Neostigmine Methylsulfate Injection is administered, it is recommended that Atropine Sulfate (0.6 to 1.2 mg) also be given intravenously using separate syringes.
- The optimum time for administration of the drug is during hyperventilation when the carbon dioxide level of the blood is low.
- It should never be administered in the presence of high concentrations of halothane or cyclopropane.
- In cardiac cases and severely ill patients, it is advisable to titrate the exact dose of Neostigmine Methylsulfate required, using a peripheral nerve stimulator device.
- In the presence of bradycardia, the pulse rate should be increased to about 80/minute with Atropine before administering Neostigmine.
Off-Label Use and Dosage (Adult)
Guideline-Supported Use
There is limited information regarding Off-Label Guideline-Supported Use of Neostigmine methylsulfate in adult patients.
Non–Guideline-Supported Use
- Paralytic ileus
- In dose increments of 0.05 mg to a total dose of 0.75 mg or to the induction of passage of flatus [1]
- To prolong postoperative peripheral block anesthesia
- Postoperative peripherally administration for analgesia
- Pseudo-obstruction of intestine
Pediatric Indications and Dosage
FDA-Labeled Indications and Dosage (Pediatric)
There is limited information regarding Neostigmine methylsulfate FDA-Labeled Indications and Dosage (Pediatric) in the drug label.
Off-Label Use and Dosage (Pediatric)
Guideline-Supported Use
There is limited information regarding Off-Label Guideline-Supported Use of Neostigmine methylsulfate in pediatric patients.
Non–Guideline-Supported Use
There is limited information regarding Off-Label Non–Guideline-Supported Use of Neostigmine methylsulfate in pediatric patients.
Contraindications
- Patients with known hypersensitivity to the drug.
- Patients with peritonitis or mechanical obstruction of the intestinal or urinary tract.
Warnings
- Should be used with caution in patients with epilepsy, bronchial asthma, bradycardia, recent coronary occlusion, vagotonia, hyperthyroidism, cardiac arrhythmias or peptic ulcer.
- When large doses of Neostigmine are administered, the prior or simultaneous injection of Atropine Sulfate may be advisable. Separate syringes should be used for the Neostigmine and Atropine. Because of the possibility of hypersensitivity in an occasional patient, Atropine and anti-shock medication should always be readily available.
Adverse Reactions
Clinical Trials Experience
Side effects are generally due to an exaggeration of pharmacological effects of which salivation and fasciculation are the most common. Bowel cramps and diarrhea may also occur.
The following additional adverse reactions have been reported following the use of either Neostigmine Bromide or Neostigmine Methylsulfate.
- Allergic: Allergic reactions and anaphylaxis.
- Neurologic: Dizziness, convulsions, loss of consciousness, drowsiness, headache, dysarthria, miosis and visual changes.
- Cardiovascular: Cardiac arrhythmias (including bradycardia, tachycardia, A-V block and nodal rhythm) and nonspecific EKG changes have been reported, as well as cardiac arrest, syncope and hypotension. These have been predominantly noted following the use of the injectable form of Neostigmine Methylsulfate.
- Respiratory: Increased oral, pharyngeal and bronchial secretions, dyspnea, respiratory depression, respiratory arrest and bronchospasm.
- Dermatologic: Rash and urticaria.
- Gastrointestinal: Nausea, emesis, flatulence and increased peristalsis.
- Genitourinary: Urinary frequency.
- Musculoskeletal: Muscle cramps and spasms, arthralgia.
- Miscellaneous: Diaphoresis, flushing and weakness.
Postmarketing Experience
There is limited information regarding Neostigmine methylsulfate Postmarketing Experience in the drug label.
Drug Interactions
- Neostigmine methylsulfate injection does not antagonize, and may in fact prolong, the Phase 1 block of depolarizing muscle relaxants such as succinylcholine or decamethonium.
- Certain antibiotics, especially neomycin, streptomycin and kanamycin, have a mild but definite nondepolarizing blocking action which may accentuate neuromuscular block.
- These antibiotics should be used in the myasthenic patient only where definitely indicated, and then careful adjustment should be made of the anticholinesterase dosage.
- Local and some general anesthetics, antiarrhythmic agents and other drugs that interfere with neuromuscular transmission should be used cautiously, if at all, in patients with myasthenia gravis; the dose of Neostigmine Methylsulfate may have to be increased accordingly.
Use in Specific Populations
Pregnancy
Pregnancy Category (FDA): C
There are no adequate or well-controlled studies of Neostigmine Methylsulfate in either laboratory animals or in pregnant women. It is not known whether Neostigmine can cause fetal harm when administered to a pregnant woman or can affect reproductive capacity. Neostigmine Methylsulfate Injection, USP should be given to a pregnant woman only if clearly needed.
Pregnancy Category (AUS): B2
There is no Australian Drug Evaluation Committee (ADEC) guidance on usage of Neostigmine methylsulfate in women who are pregnant.
Labor and Delivery
There is no FDA guidance on use of Neostigmine methylsulfate during labor and delivery.
Nursing Mothers
It is not known whether neostigmine methylsulfate is excreted in human milk. Because many drugs are excreted in human milk and because of the potential for serious adverse reactions from Neostigmine Methylsulfate 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
Pediatric Use
Safety and effectiveness in children have not been established.
Geriatic Use
There is no FDA guidance on the use of Neostigmine methylsulfate in geriatric settings.
Gender
There is no FDA guidance on the use of Neostigmine methylsulfate with respect to specific gender populations.
Race
There is no FDA guidance on the use of Neostigmine methylsulfate with respect to specific racial populations.
Renal Impairment
There is no FDA guidance on the use of Neostigmine methylsulfate in patients with renal impairment.
Hepatic Impairment
There is no FDA guidance on the use of Neostigmine methylsulfate in patients with hepatic impairment.
Females of Reproductive Potential and Males
Studies on the effect of Neostigmine Methylsulfate on fertility and reproduction have not been performed.
Immunocompromised Patients
There is no FDA guidance one the use of Neostigmine methylsulfate in patients who are immunocompromised.
Administration and Monitoring
Administration
Intravenous
Monitoring
Only in exceptional cases should the total dose of Neostigmine Methylsulfate exceed 5 mg. It is recommended that the patient be well ventilated and a patent airway maintained until complete recovery of normal respiration is assured.
IV Compatibility
There is limited information regarding the compatibility of Neostigmine methylsulfate and IV administrations.
Overdosage
Overdosage of neostigmine methylsulfate can cause cholinergic crisis, which is characterized by increasing muscle weakness, and through involvement of the muscles of respiration, may result in death. Myasthenic crisis, due to an increase in the severity of the disease, is also accompanied by extreme muscle weakness and may be difficult to distinguish from cholinergic crisis on a symptomatic basis. However, such differentiation is extremely important because increases in the dose of Neostigmine Methylsulfate or other drugs in this class, in the presence of cholinergic crisis or of a refractory or “insensitive” state, could have grave consequences. The two types of crises may be differentiated by the use of edrophonium chloride as well as by clinical judgement. Treatment of the two conditions differs radically. Whereas the presence of myasthenic crisis requires more intensive anticholinesterase therapy, cholinergic crisis calls for the prompt withdrawal of all drugs of this type. The immediate use of Atropine in cholinergic crisis is also recommended. Atropine may also be used to abolish or minimize gastrointestinal side effects or other muscarinic reactions; but such use, by masking signs of overdosage, can lead to inadvertent induction of cholinergic crisis.
The LD50 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 LD50 is 0.315 ± 0.019 mg/kg intravenously, 0.445 ± 0.032 mg/kg subcutaneously and 0.423 ± 0.032 mg/kg intramuscularly.
Pharmacology
Mechanism of Action
There is limited information regarding Neostigmine methylsulfate Mechanism of Action in the drug label.
Structure
There is limited information regarding Neostigmine methylsulfate Structure in the drug label.
Pharmacodynamics
There is limited information regarding Neostigmine methylsulfate Pharmacodynamics in the drug label.
Pharmacokinetics
There is limited information regarding Neostigmine methylsulfate Pharmacokinetics in the drug label.
Nonclinical Toxicology
There is limited information regarding Neostigmine methylsulfate Nonclinical Toxicology in the drug label.
Clinical Studies
There is limited information regarding Neostigmine methylsulfate Clinical Studies in the drug label.
How Supplied
There is limited information regarding Neostigmine methylsulfate How Supplied in the drug label.
Storage
There is limited information regarding Neostigmine methylsulfate Storage in the drug label.
Images
Drug Images
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Package and Label Display Panel
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Patient Counseling Information
There is limited information regarding Neostigmine methylsulfate Patient Counseling Information in the drug label.
Precautions with Alcohol
Alcohol-Neostigmine methylsulfate interaction has not been established. Talk to your doctor about the effects of taking alcohol with this medication.
Brand Names
There is limited information regarding Neostigmine methylsulfate Brand Names in the drug label.
Look-Alike Drug Names
There is limited information regarding Neostigmine methylsulfate Look-Alike Drug Names in the drug label.
Drug Shortage Status
Price
References
The contents of this FDA label are provided by the National Library of Medicine.
- ↑ Heimbach DM, Crout JR (1971). "Treatment of paralytic ileus with adrenergic neuronal blocking drugs". Surgery. 69 (4): 582–7. PMID 4928770.