Neomycin and polymyxin B (Maxitrol) - Uses, Dose, Side effects, MOA

Neomycin and polymyxin B (Maxitrol) is a combination of non-absorbable antibiotics that are used for bladder irrigation in patients who develop bacteriuria due to prolonged bladder catheterization.

Neomycin and polymyxin B (Maxitrol) Uses:

  • Urinary bladder irrigant:

    • It is used as a bladder irrigant (for short-term use of up to 10 days) in patients who have bacteriuria due to the use of long-term indwelling catheters to prevent bacteria and septicemia.

Neomycin and polymyxin B (Maxitrol) Dose in Adults

Neomycin and polymyxin B Dose in the treatment of Urinary bladder irrigant:

  • Intravesical:
    • Add 1 mL irrigant to 1,000 ml isotonic saline solution per day as continuous irrigation for up to 10 days.

Neomycin and polymyxin B (Maxitrol) Dose in Children

Neomycin and polymyxin B Dose in the treatment of Urinary bladder irrigant:

Note: The data is limited and the effectiveness of the drug varies. Most of the experience with the drug has been in patients with spinal cord injury or neurogenic bladder.

  • Children and Adolescents:

    • Irrigant solution (neomycin 40 mg/polymyxin B 200,000 units/L):
      • Intravesical: 10 mL instilled at the end of each catheterization and retained until next catheterization.
      • In older adolescents, 30 mL 2 to 3 times daily has been used for asymptomatic bacteriuria.
    • Note: Use has generally been replaced with other agents (eg, saline, gentamicin).

Pregnancy Category: C

  • Studies on animal reproduction have not been carried out using this mixture.
  • There are reports of total irreversible bilateral congenital deafness in children whose mothers received streptomycin during pregnancy.
  • Talk to individual agents.

Use during breastfeeding:

 

  • The drug's potential for excretion into breastmilk is unknown.

Dose in Kidney Disease:

The manufacturer has not recommended any adjustments in the dose in patients with kidney disease.

Dose in Liver disease:

The manufacturer has not recommended any adjustments in the dose in liver disease.

Side effects of Neomycin and polymyxin B (Maxitrol):

  • Central Nervous System:

    • Localized Burning
  • Dermatologic:

    • Contact Dermatitis
    • Erythema
    • Skin Rash
    • Urticaria
  • Genitourinary:

    • Bladder Mucosa Irritation
    • Nephrotoxicity
  • Neuromuscular & Skeletal:

    • Neuromuscular Blockade
  • Otic:

    • Ototoxicity

Contraindications to Neomycin and polymyxin B (Maxitrol):

  • Neomycin, neomycin B, or any other ingredient of the formulation-related allergic responses
  • those who have previously experienced severe allergic responses to aminoglycosides.

Warnings and precautions

  • Superinfection

    • Long-term use of the drug can lead to fungal and bacterial superinfections, such as C. difficile-associated diarrhea or pseudomembranous collitis.
    • CDAD can occur even after two months of last antibiotic use.
  • Systemic toxicities:

    • Systemic absorption may lead to nephrotoxicity, ototoxicity, or neuromuscular blockade.
    • Systemic absorption can be more common in patients who have bladder defects or who have had surgery that has caused injury to the bladder wall.
  • Renal impairment

    • It can increase the risk of kidney toxicity. You should use it with caution.

Neomycin and polymyxin B: Drug Interaction

Risk Factor C (Monitor therapy)

Acarbose

Neomycin may enhance the adverse/toxic effect of Acarbose. Neomycin may decrease the metabolism of Acarbose.

Amphotericin B

Aminoglycosides' nephrotoxic effects might be amplified.

Arbekacin

Aminoglycosides' nephrotoxic effects might be amplified. Arbekacin may make aminoglycosides more ototoxic.

BCG Vaccine (Immunization)

Antibiotics may reduce the BCG vaccine's therapeutic effect (Immunization).

Bisphosphonate Derivatives

The hypocalcemic action of bisphosphonate derivatives may be enhanced by aminoglycosides.

Botulinum Toxin-Containing Products

The neuromuscularblocking action of products containing botulinum toxin may be enhanced by aminoglycosides.

Capreomycin

May strengthen Polymyxin B's ability to impede neuromuscular transmission.

CARBOplatin

Aminoglycosides may increase CARBOplatin's ototoxic effects. especially when carboplatin doses are higher.

Cardiac Glycosides

Cardiac Glycosides' serum levels may be lowered by aminoglycosides. Only oral aminoglycoside treatment has proven to have this effect.

Cefazedone

May intensify Polymyxin B's nephrotoxic effects.

Cephalosporins (2nd Generation)

Aminoglycosides' nephrotoxic effects might be amplified.

Cephalosporins (3rd Generation)

Aminoglycosides' nephrotoxic effects might be amplified.

Cephalosporins (4th Generation)

Aminoglycosides' nephrotoxic effects might be amplified.

Cephalothin

Aminoglycosides' nephrotoxic effects might be amplified.

Cephradine

Aminoglycosides' nephrotoxic effects might be amplified.

CISplatin

Aminoglycosides' nephrotoxic effects might be amplified.

CycloSPORINE (Systemic)

Aminoglycosides may increase CycloSPORINE's nephrotoxic effects (Systemic).

Distigmine

Aminoglycosides may reduce Distigmine's therapeutic efficacy.

Lactobacillus and Estriol

The therapeutic effects of Lactobacillus and Estriol may be reduced by antibiotics.

Loop Diuretics

Aminoglycosides' harmful or poisonous effects could be amplified. ototoxicity and nephrotoxicity in particular.

Nonsteroidal Anti-Inflammatory Agents

Aminoglycosides' excretion may be reduced. only information on preterm newborns.

Oxatomide

Aminoglycosides' nephrotoxic effects might be amplified.

Regorafenib

The active metabolite(s) of Regorafenib's serum concentrations may be lowered by neomycin.

SORAfenib

It's possible that neomycin will lower SORAfenib's serum levels.

Tenofovir Products

Tenofovir products' serum concentration may be raised by aminoglycosides. Aminoglycoside content in the serum may rise as a result of using tenofovir products.

Vancomycin

Aminoglycosides' nephrotoxic effects might be amplified.

Vitamin K Antagonists (eg, warfarin)

The anticoagulant action of Vitamin K antagonists may be enhanced by neomycin.

Risk Factor D (Consider therapy modification)

Colistimethate

Colistimethate's nephrotoxic action may be increased by aminoglycosides. Colistimethate's ability to suppress neuromuscular activity may be improved by aminoglycosides.

Neuromuscular-Blocking Agents

The neuromuscular-blocking effects of neuromuscular-blocking agents may be strengthened by polymyxin B.

Penicillins

Aminoglycosides' serum levels could drop. mainly found in patients with renal impairment and extended spectrum penicillins. Penicillin G (Parenteral/Aqueous); Penicillin G Benzathine; Penicillin G Procaine; Penicillin V Benzathine; Penicillin V Potassium; are exceptions to this rule. Other exceptions are Amoxicillin, Ampicillin, Bacampicillin, Cloxacillin, Dicloxacillin, Nafcillin, and Oxacillin.

Sodium Picosulfate

Antibiotics may reduce Sodium Picosulfate's therapeutic impact. Management: If a patient previously used or is currently using an antibiotic, think about utilising an alternative product for bowel cleansing prior to a colonoscopy.

Risk Factor X (Avoid combination)

Ataluren

Aminoglycosides' harmful or poisonous effects could be amplified. Specifically, using ataluren and aminoglycosides simultaneously may result in an elevated risk of nephrotoxicity.

Bacitracin (Systemic)

Polymyxin B may increase Bacitracin's nephrotoxic effects (Systemic).

Bacitracin (Systemic)

Neomycin may intensify Bacitracin's nephrotoxic effects (Systemic).

BCG (Intravesical)

Antibiotics may lessen BCG's therapeutic effects (Intravesical).

Cholera Vaccine

Antibiotics may diminish the therapeutic effect of Cholera Vaccine. Management: Avoid cholera vaccine in patients receiving systemic antibiotics, and within 14 days following the use of oral or parenteral antibiotics.

Foscarnet

Aminoglycosides' nephrotoxic effects might be amplified.

Mannitol (Systemic)

Aminoglycosides' nephrotoxic effects might be amplified.

Mecamylamine

Mecamylamine's ability to suppress neuromuscular activity could be improved by polymyxin B.

Methoxyflurane

May intensify Polymyxin B's nephrotoxic effects

Monitoring parameters:

  • Urinalysis,
  • renal function.

How to administer Neomycin and polymyxin B?

  • It is indicated only for the irrigation of the bladder and not for parenteral administration.
  • The inflow lumen of the 3-way catheter should be connected to the irrigation container to allow the continuous irrigation of the urinary bladder.
  • The bladder rinse should be continuous and the irrigation should not be interrupted for more than a few minutes.
  • The flow rate of the irrigation should be adjusted to 1 liter per 24 hours.
  • However, if the patients' urine output exceeds 2 liters per 24 hours, the flow rate should be set at a rate of 2 liters per 24 hours.

Mechanism of action of Neomycin and polymyxin B:

Neomycin:

  • It binds with the 30S subunit of the ribosomal ribosomal subunit, inhibits bacterial protein synthesis, and indirectly inhibits bacterial replication.

Polymyxin B

  • By binding to phospholipids, it damages the bacterial cell membrane. It causes a decrease in bacterial cellular permeability, which allows for the leakage intracellular content.

Talk to individual agents.

Absorption:

 

  • It is only minimally absorbed when used topically. Systemic absorption can occur if the bladder is inflamed or denuded.

International Brands of Neomycin and polymyxin B:

  • Neosporin G.U. Irrigant
  • Neosporin Irrigating Solution
  • Alosol
  • Isopto Statrol
  • Maxitrol
  • Statrol

Neomycin and polymyxin B Brands Names in Pakistan:

  • Maxitrol