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Brand Name :
Zemdri
Synonyms :
plazomicin
Class :
Aminoglycosides
Dosage forms & Strengths:Â
Adult:Â
Single-use injectionÂ
500 mg/10mLÂ
Safety and efficacy are not seen in pediatrics
Refer to the adult dosing, and reduce the dose as per renal impairment condition
Actions and Spectrum:Â
plazomicin is an aminoglycoside antibiotic that is used to treat serious bacterial infections caused by certain gram-negative bacteria. It is active against a broad spectrum of gram-negative bacteria, including Enterobacteriaceae (such as Escherichia coli, Klebsiella pneumoniae, and Enterobacter cloacae) and Pseudomonas aeruginosa.Â
plazomicin has a bactericidal mode of action, which means it kills bacteria directly. It acts by binding to the bacterial 30S ribosomal subunit and inhibiting protein synthesis. This leads to the formation of mistranslated proteins, which causes the bacterial cell to die.Â
1-10%:Â
Decreased renal function (3.6%)Â
Diarrhea (2.3%)Â
Headache (1.3%)Â
Hypotension (1%)Â
Nausea (1.3%)Â
Treatment-related ototoxicity (2.2%)Â
Black Box Warning:Â
It is essential to follow the dosage and administration instructions for the medication carefully.
Contraindication/Caution:Â
plazomicin should not be used in people hypersensitive to the drug itself.Â
Pregnancy consideration:Â Â
Females of reproductive potential are advised not to become pregnant during the treatment. The drug may cause harm to the fetus.Â
Breastfeeding warnings:Â Â
No data is available regarding the presence of the drug in breast milk.Â
Pregnancy category:Â
PharmacologyÂ
plazomicin is an aminoglycoside antibiotic that acts by binding to the bacterial ribosome and inhibiting protein synthesis. It causes bacterial death and the elimination of the infection. plazomicin is active against a broad spectrum of gram-negative bacteria, including Enterobacteriaceae (such as Escherichia coli, Klebsiella pneumoniae, and Enterobacter cloacae) and Pseudomonas aeruginosa.Â
Pharmacodynamics:Â
The pharmacodynamic properties of plazomicin are characterized by a high bacterial killing activity and low emergence of resistance. The drug is usually administered intravenously and has a rapid onset of action, making it an effective treatment option for serious bacterial infections caused by multidrug-resistant bacteria. Pharmacokinetics:Â
plazomicin is typically administered intravenously, and it has a rapid onset of action. Following intravenous administration, the drug is rapidly and completely absorbed, with peak plasma concentrations occurring within 30 minutes. The volume of distribution of plazomicin is relatively low, around 0.3 L/kg. The drug is eliminated through kidneys through glomerular filtration and tubular secretion. The elimination half-life of plazomicin is about 1-2 hours.Â
AbsorptionÂ
The peak plasma concentration is 73.7 mcg/ml for healthy subjects. Whereas 51 mcg/ml for chronic subjects.Â
The AUC is 257 mcg·hr/mL for healthy subjects. Whereas 226 mcg·hr/mL for chronic subjectsÂ
DistributionÂ
The percent of bound protein is 20%Â
The volume of distribution is 17.9 L for healthy subjects. Whereas 30.8L for chronic subjects.Â
MetabolismÂ
plazomicin does not metabolize up to a great extent. Â
Elimination and excretionÂ
The half-life of plazomicin is 3.5 hours, and 4.5L/hr is the clearance rate.
Administration:Â
plazomicin is administered through an intravenous route. It is compatible with 0.9% NaCl or Ringer solution. Do not mix other drugs with the solution.
Patient information leafletÂ
Generic Name: plazomicinÂ
Pronounced: plah-zoh-mis-inÂ
Why do we use plazomicin?Â
plazomicin is an aminoglycoside. It helps in the treatment of various Urinary Tract Infections.     Â