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Hexamycin

Active Ingredient:
Gentamicin
Origin:
EU

Hexamycin (Gentamicin)

Hexamycin is an injectable antibiotic that contains the aminoglycoside gentamicin as its active ingredient. It is supplied in a sterile solution for intramuscular or intravenous administration and is marketed within the European Union. As a prescription‑only product, Hexamycin is used under medical supervision to treat serious bacterial infections, particularly those caused by gram‑negative organisms. The formulation follows standard EU pharmaceutical quality and regulatory compliance guidelines.

Manufacturer / TM Owner

Sandoz A/S

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Indications & Clinical Uses

Hexamycin is indicated for the treatment of severe bacterial infections where rapid bactericidal activity is required.

  • Severe sepsis and septic shock caused by susceptible gram‑negative bacteria.
  • Hospital‑acquired pneumonia, including ventilator‑associated pneumonia, due to susceptible organisms.
  • Complicated urinary tract infections and pyelonephritis when gram‑negative pathogens are identified.
  • Intra‑abdominal infections such as peritonitis with documented susceptibility.
  • Bone and joint infections caused by gram‑negative bacteria, used in combination therapy.
  • Neonatal infections caused by gram‑negative organisms, administered under specialist guidance.

How It Works

  • Gentamicin exerts its antibacterial effect by binding irreversibly to the 30S subunit of bacterial ribosomes. This interaction disrupts the initiation complex and induces misreading of messenger RNA, leading to the production of abnormal proteins. The resulting protein synthesis inhibition is bactericidal, particularly against aerobic gram‑negative organisms, and contributes to rapid reduction of bacterial load in systemic infections. It also interferes with the integrity of the bacterial cell membrane, enhancing uptake of the drug.

Side Effects

Adverse reactions to Hexamycin may range from mild, transient symptoms to rare but serious events requiring medical attention.

Common

  • Nephrotoxicity manifested as increased serum creatinine or reduced urine output.
  • Ototoxicity presenting as tinnitus, hearing loss, or balance disturbances.
  • Neuromuscular blockade causing muscle weakness, especially in patients with underlying disorders.
  • Injection site reactions such as pain, erythema, or swelling.

Serious

  • Acute kidney injury leading to oliguria or anuria.
  • Permanent hearing loss or vestibular dysfunction.
  • Severe allergic reactions including anaphylaxis.
  • Respiratory paralysis in patients with myasthenia gravis.

Precautions & Warnings

Use of Hexamycin requires careful assessment of patient risk factors and monitoring to minimize toxicity.

  • Assess renal function before initiation and monitor serum creatinine during therapy.
  • Perform baseline and periodic audiometric testing, especially in prolonged courses.
  • Adjust dose in patients with impaired kidney function or elderly individuals.
  • Avoid use in patients with known hypersensitivity to aminoglycosides.
  • Use with caution in neonates, pregnant or breastfeeding women due to limited safety data.
  • Monitor neuromuscular function in patients with myasthenia gravis or receiving neuromuscular blockers.

Avoid Interactions

Hexamycin can interact with other medicines, altering its efficacy or increasing the risk of toxicity.

Avoid

  • Concurrent use with other nephrotoxic agents such as vancomycin, amphotericin B, or loop diuretics.
  • Co‑administration with potent neuromuscular blockers (e.g., pancuronium) that may exacerbate paralysis.

Use with caution

  • Concurrent therapy with other ototoxic drugs like loop diuretics or cisplatin.
  • Use with other aminoglycosides or high‑dose penicillins that may affect renal clearance.
  • Combination with diuretics may increase serum gentamicin concentrations.
  • When given with drugs that affect serum potassium, monitor electrolytes closely.

Frequently Asked Questions

Hexamycin is used for severe bacterial infections, especially those caused by gram‑negative organisms such as sepsis, hospital‑acquired pneumonia, complicated urinary tract infections, intra‑abdominal infections, bone and joint infections, and certain neonatal infections.

Hexamycin is supplied as a sterile injectable solution and can be given either intramuscularly or intravenously under the supervision of a qualified healthcare professional.

Patients with impaired renal function require dose adjustment and close monitoring of serum creatinine and urine output because gentamicin can be nephrotoxic.

Regular assessment of renal function, baseline and periodic hearing tests, and observation for signs of neuromuscular weakness are recommended to detect early toxicity.

The safety of Hexamycin in pregnancy has not been established; it should be used only if the potential benefit justifies the potential risk to the fetus.

Common adverse effects include nephrotoxicity, ototoxicity (tinnitus, hearing loss), neuromuscular blockade, and local injection‑site reactions such as pain or erythema.

Serious reactions may include acute kidney injury, permanent hearing loss or vestibular dysfunction, severe allergic reactions such as anaphylaxis, and respiratory paralysis in patients with myasthenia gravis.

Concurrent use of other nephrotoxic agents (e.g., vancomycin, amphotericin B, loop diuretics) and potent neuromuscular blockers should be avoided because they increase the risk of toxicity.

Caution is advised when Hexamycin is combined with other ototoxic drugs (e.g., cisplatin), other aminoglycosides, high‑dose penicillins, diuretics, or medications that affect serum potassium levels.

Gentamicin, the active ingredient in Hexamycin, binds to the bacterial 30S ribosomal subunit, causing misreading of mRNA and production of faulty proteins, which leads to rapid bacterial cell death.

No, Hexamycin is a prescription‑only medication and must be prescribed by a qualified healthcare professional.

Patients should report any tinnitus, hearing loss, or balance issues immediately to their healthcare provider for evaluation and possible discontinuation of therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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