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Fytobra 80mg Injection 1s is a potent aminoglycoside antibiotic used to treat serious bacterial infections. It works by stopping the growth of bacteria by interfering with their ability to produce essential proteins. It is particularly effective against Gram-negative bacteria, including Pseudomonas aeruginosa. Fytobra 80mg Injection 1s is commonly used to treat lung infections in patients with cystic fibrosis, severe systemic infections, and various infections of the eyes and skin. It is available in multiple formulations, including solutions for injection, liquid for inhalation (nebulization), and topical eye drops or ointments.
Fytobra 80mg Injection 1s contains tobramycin, an antibiotic derived from the Streptomyces tenebrarius bacterium. It belongs to the aminoglycoside class of medications, which are known for their rapid bactericidal action (ability to kill bacteria) against a broad spectrum of aerobic Gram-negative bacilli.
The medication works by binding to the 30S subunit of the bacterial ribosome. This binding causes misreading of the genetic code and prevents the bacteria from synthesising the proteins they need to survive and multiply. Because it disrupts the integrity of the bacterial cell membrane, it effectively kills the bacteria rather than just inhibiting their growth.
Clinically, Fytobra 80mg Injection 1s may be used in several specialised settings. In patients with cystic fibrosis, inhaled formulations may be used to help manage chronic lung infections and support respiratory function. In hospital settings, the injectable form can be used for serious infections such as sepsis, meningitis, or complicated urinary tract infections. Topical ophthalmic formulations may be prescribed for bacterial eye infections such as conjunctivitis or keratitis.
Because aminoglycosides carry a risk of affecting kidney and hearing function (particularly systemic (injectable) treatment), it requires careful monitoring of blood levels and renal function. Fytobra 80mg Injection 1s is intended for use under strict medical supervision to ensure the infection is cleared safely while minimising potential toxicity.
Fytobra 80mg Injection 1s may be indicated by your doctor for:
Inhaled maintenance therapy to manage chronic Pseudomonas aeruginosa infections in the lungs.
Injectable treatment for sepsis, lower respiratory tract infections, and complicated intra-abdominal infections.
Topical treatment for conjunctivitis, blepharitis, and other external ocular infections caused by bacteria.
For complicated or recurrent bacterial infections of the urinary system.
To treat serious infections of the skeletal system caused by susceptible bacteria.
Management of severe infected wounds or burns when caused by Gram-negative bacteria.
Fytobra 80mg Injection 1s may provide benefits such as:
Fytobra 80mg Injection 1s may cause side effects in some people (depending on the type of formulation prescribed), although many tolerate it well when used as prescribed.
Use Fytobra 80mg Injection 1s exactly as directed by your doctor based on the prescribed form.
Fytobra 80mg Injection 1s works by targeting the internal machinery of bacterial cells. It enters the bacteria and binds to the 30S ribosomal subunit. This binding disrupts the translation of messenger RNA (mRNA) into proteins. Without these essential proteins, the bacteria cannot maintain their cell walls, replicate their DNA, or perform basic life functions. Additionally, tobramycin causes the bacterial cell membrane to become "leaky," leading to rapid cell death. This direct killing mechanism makes it a powerful tool against aggressive and fast-growing bacterial colonies.
Tobramycin should only be used if clearly needed, as aminoglycosides may pose risks to the fetus.
Tobramycin can pass into breast milk in small amounts; caution is advised when nursing.
Tobramycin may cause dizziness or balance problems in some patients. Avoid driving or operating machinery until you know how it affects you.
Generally safe, as Tobramycin is not extensively metabolised by the liver, but monitoring is recommended in patients with liver disease.
Tobramycin is eliminated primarily by the kidneys; dose adjustments and close monitoring are essential in patients with renal impairment.
Alcohol may worsen dizziness or balance issues, increasing the risk of side effects.
An overdose of Fytobra 80mg Injection 1s containing Tobramycin is uncommon when used as prescribed. Using more than recommended over time may increase the chance of side effects, particularly affecting the kidneys or hearing. Some people may notice symptoms such as mild dizziness, ringing in the ears, or changes in urine output. With topical forms, effects are usually limited to local irritation. If you think more than the prescribed amount has been used, it is best to speak with your doctor for guidance.
If you miss a dose, use it as soon as you remember. If it is almost time for your next dose, skip the missed one and return to your regular schedule. Do not use a double dose to make up for a forgotten one. If you miss a dose of the injectable form, contact your healthcare provider immediately.
Therapeutic Class
Antibacterial Agent
Action Class
Protein Synthesis Inhibitor (30S Ribosome)
Chemical Class
Chemical Class Aminoglycoside Antibiotic
Habit Forming
No
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