About The Drug Levofloxacin Ophthalmic Solution 1.5% aka Iquix
![ClusterMed ClusterMed](/images/clustermed.jpg)
Find Levofloxacin Ophthalmic Solution 1.5% side effects, uses, warnings, interactions and indications. Levofloxacin Ophthalmic Solution 1.5% is also known as Iquix.
Levofloxacin Ophthalmic Solution 1.5%
![Levofloxacin Ophthalmic Solution 1.5% Prescription Drug Bottle Levofloxacin Ophthalmic Solution 1.5% Prescription Drug Bottle](/images/prescriptiondrugbottle.jpg)
About Levofloxacin Ophthalmic Solution 1.5% aka Iquix |
---|
What's The Definition Of The Medical Condition Levofloxacin Ophthalmic Solution 1.5%?Clinical Pharmacology CLINICAL PHARMACOLOGY Mechanism Of Action Levofloxacin is a member of the fluoroquinolone class of anti-microbial drug (See Microbiology).
Pharmacokinetics Levofloxacin concentration in plasma was measured in 14 healthy adult volunteers during a 16day course of treatment with IQUIX® solution.
The dosing schedule was 1-2 drops per eye once in the morning on Days 1 and 16; 1-2 drops per eye every two hours Days 2 through 8; and 1-2 drops per eye every four hours Days 9 through 15.
The mean levofloxacin concentration in plasma 1 hour post dose ranged from 3.13 ng/mL on Day 1 to 10.4 ng/mL on Day 16.
Maximum mean levofloxacin concentrations increased from 3.22 ng/mL on Day 1 to 10.9 ng/mL on Day 16, which is more than 400 times lower than those reported after standard oral doses of levofloxacin.
Levofloxacin concentration in tears was measured in 100 healthy adult volunteers at various time points following instillation of 2 drops of IQUIX® solution.
Mean tear concentration measured 15 minutes after instillation was 757 mcg/mL.
Microbiology Levofloxacin is the L-isomer of the racemate, ofloxacin, a quinolone antimicrobial agent.
The antibacterial activity of ofloxacin resides primarily in the L-isomer.
The mechanism of action of levofloxacin and other fluoroquinolone antimicrobials involves the inhibition of bacterial topoisomerase IV and DNA gyrase (both of which are type II topoisomerases), enzymes required for DNA replication, transcription, repair, and recombination.
Levofloxacin has in vitro activity against a wide range of Gram-negative and Gram-positive microorganisms and is often bactericidal at concentrations equal to or slightly greater than inhibitory concentrations.
Fluoroquinolones, including levofloxacin, differ in chemical structure and mode of action from ß-lactam antibiotics and aminoglycosides, and therefore may be active against bacteria resistantto ß-lactam antibiotics and aminoglycosides.
Additionally, ß-lactam antibiotics andaminoglycosides may be active against bacteria resistant to levofloxacin.
Resistance tolevofloxacin due to spontaneous mutation in vitro is a rare occurrence (range: 10 -9 to 10-10).
Levofloxacin has been shown to be active against most strains of the following microorganisms, both in vitro and in clinical infections as described in the INDICATIONS AND USAGE section .
Aerobic Gram-positive Microorganisms Corynebacterium species* Staphylococcus aureus Staphylococcus epidermidis Streptococcus pneumoniae Viridans group streptococci* Aerobic Gram-negative Microorganisms Pseudomonas aeruginosa Serratia marcescens* *Efficacy for this organism was studied in fewer than 10 infections.
The following in vitro data are also available, but their clinical significance in ophthalmic infections is unknown.
The safety and effectiveness of levofloxacin in treating ophthalmological infections due to these microorganisms have not been established in adequate and well controlled trials.
These organisms are considered susceptible when evaluated using systemic breakpoints.
However, a correlation between the in vitro systemic breakpoint and ophthalmological efficacy has not been established.
The list of organisms is provided as guidance only in assessing the potential treatment of corneal ulcer.
Levofloxacin exhibits in vitro minimal inhibitory concentrations (MICs) of 2 mcg/mL or less (systemic susceptible breakpoint) against most ( ≥ 90%) strains of the following ocular pathogens: Aerobic Gram-positive Microorganisms Enterococcus faecalis (many strains are only moderately susceptible) Staphylococcus saprophyticus Streptococcus agalactiae Streptococcus pyogenes Streptococcus (Group C/F) Streptococcus (Group G) Aerobic Gram-negative Microorganisms Acinetobacter baumannii Acinetobacter lwoffii Citrobacter koseri Citrobacter freundii Enterobacter aerogenes Enterobacter cloacae Escherichia coli Haemophilus influenzae Haemophilus parainfluenzae Klebsiella oxytoca Klebsiella pneumonia Legionella pneumophila Moraxella catarrhalis Morganella morganii Neisseria gonorrhoeae Pantoea agglomerans Proteus mirabilis Proteus vulgaris Providencia rettgeri Providencia stuartii Pseudomonas fluorescens Clinical Studies In two randomized, double-masked, multi-center, controlled clinical trials of 280 patients with positive cultures, subjects were dosed with IQUIX® or ofloxacin 0.3% ophthalmic solution.
Dosing occurred on Days 1 through 3 every two hours while awake and 4 and 6 hours after retiring.
Dosing occurred on Day 4 through treatment completion 4 times daily while awake.
Clinical cure was defined as complete re-epithelialization and no progression of the infiltrate for two consecutive visits.
The IQUIX® treated subjects had an approximately equal mean clinical cure rate of 80% (73% to 87%) compared to 84% (82% to 86%) for the subjects treated with ofloxacin 0.3% ophthalmic solution.
Drug Description IQUIX® (levofloxacin) Ophthalmic Solution DESCRIPTION IQUIX® (levofloxacin ophthalmic solution) 1.5% is a sterile topical ophthalmic solution.
Levofloxacin is a fluoroquinolone antibacterial active against a broad spectrum of Gram-positive and Gram-negative ocular pathogens.
Levofloxacin is a fluorinated 4-quinolone containing a six-member (pyridobenzoxazine) ring from positions 1 to 8 of the basic ring structure.
Levofloxacin is the pure (-)-(S)-enantiomer of the racemic drug substance, ofloxacin.
It is more soluble in water at neutral pH than ofloxacin.
C18H20F3O4 • ½H2O Mol Wt 370.38 Chemical Name: (-)-(S)-9-fluoro-2,3-dihydro-3-methyl-10-(4-methyl-1-piperazinyl)-7-oxo-7Hpyrido[1,2,3-de]-1,4 benzoxazine-6-carboxylic acid hemihydrate.
Levofloxacin (hemihydrate) is a yellowish-white crystalline powder.
Each mL of IQUIX® contains 15.36 mg of levofloxacin hemihydrate equivalent to 15 mg levofloxacin.
Contains: Active: Levofloxacin 1.5% (15 mg/mL); Inactives: glycerin and water.
May also contain hydrochloric acid and/or sodium hydroxide to adjust pH to approximately 6.5.
IQUIX® solution is isotonic with an osmolality of approximately 290 mOsm/kg.
Indications & Dosage INDICATIONS IQUIX® solution is indicated for the treatment of corneal ulcer caused by susceptible strains of the following bacteria: Gram-positive Bacteria Corynebacterium species Staphylococcus aureus Staphylococcus epidermidis Streptococcus pneumonia Viridans group streptococci* Gram-negative Bacteria Pseudomonas aeruginosa Serratia marcescens* *Efficacy for this organism was studied in fewer than 10 infections DOSAGE AND ADMINISTRATION Days 1 Through 3 Instill one to two drops in the affected eye(s) every 30 minutes to 2 hours while awake and approximately 4 and 6 hours after retiring.
Day 4 Through Treatment Completion Instill one to two drops in the affected eye(s) very 1 to 4 hours while awake.
HOW SUPPLIED Dosage Forms And Strengths 5 cc bottle filled with 5 mL sterile ophthalmic solution of levofloxacin, 1.5%.
Storage Handling IQUIX® (levofloxacin ophthalmic solution) 1.5% is supplied in a white, low density polyethylene bottle with a controlled dropper tip and a tan, high density polypropylene cap.
5mL fill in a 5cc container ---NDC 68669-145-05 Storage Store at 15° – 25°C (59° – 77°F).
Manufactured by: Santen Oy, P.O.
Box 33, FeN-33721 Tampere, Finland.
Licensed from: Daiichi Sankyo Co., Ltd., Tokyo, Japan.
Revised: November 2014
Medication Guide PATIENT INFORMATION Avoid Contamination Of The Product Advise patients to avoid contaminating the applicator tip with material from the eye, finger, or other source.
Avoid Contact Lens Wear Advise patients not to wear contact lenses if they have signs and symptoms of corneal ulcer.
Hypersensitivity Reactions Systemically administered quinolones, including levofloxacin, have been associated with hypersensitivity reactions, even following a single dose.
Advise patients to discontinue use immediately and contact their physician at the first sign of a rash or allergic reactions.
Overdosage & Contraindications OVERDOSE No information provided.
CONTRAINDICATIONS IQUIX® solution is contraindicated in patients with a history of hypersensitivity to levofloxacin, to other quinolones, or to any of the components in this medication.
Side Effects & Drug Interactions SIDE EFFECTS The most frequently reported adverse reactions in the overall study population were headache and a taste disturbance following instillation.
These reactions occurred in approximately 8-10% of patients.
Adverse reactions occurring in approximately 1-2% of patients included decreased/blurred vision, diarrhea, dyspepsia, fever, infection, instillation site irritation/discomfort, ocular infection, nausea, ocular pain/discomfort, and throat irritation.
Other reported ocular reactions occurring in less than 1% of patients included chemosis, corneal erosion, diplopia, floaters, hyperemia, lid edema, and lid erythema.
DRUG INTERACTIONS No information provided.
Warnings & Precautions WARNINGS Included as part of the PRECAUTIONS section.
PRECAUTIONS Hypersensitivity Reactions In patients receiving systemically administered quinolones, including levofloxacin, serious and occasionally fatal hypersensitivity (anaphylactic) reactions have been reported, some following the first dose.
Some reactions were accompanied by cardiovascular collapse, loss of consciousness, angioedema, (including laryngeal, pharyngeal or facial edema), airway obstruction, dyspnea, urticaria and itching.
If an allergic reaction to levofloxacin occurs, discontinue the drug.
Serious acute hypersensitivity reactions may require immediate emergency treatment.
Oxygen and airway management should be administered as clinically indicated.
Growth Of Resistant Organisms With Prolonged Use As with other anti-infectives, prolonged use may result in overgrowth of non-susceptible organisms, including fungi.
If superinfection occurs, discontinue use and institute alternative therapy.
Whenever clinical judgment dictates, the patient should be examined with the aid of magnification, such as slit-lamp biomicroscopy, and where appropriate, fluorescein staining.
Avoidance Of Contact Lens Wear Patients should be advised not to wear contact lenses if they have signs and symptoms of cornealulcer.
Nonclinical Toxicology Carcinogenesis, Mutagenesis, Impairment Of Fertility In a long term carcinogenicity study in rats, levofloxacin exhibited no carcinogenic or tumorigenic potential following daily dietary administration for 2 years at doses up to 100 mg/kg/day, corresponding to plasma levels that were 245 times maximum clinical exposure, based on Cmax.
Levofloxacin was not mutagenic in the following assays: Ames bacterial mutation assay (S.
typhimurium and E.
coli) CHO/HGPRT forward mutation assay, mouse micronucleus test, mouse dominant lethal test, rat unscheduled DNA synthesis assay, and the in vivo mouse sister chromatid exchange assay.
It was positive in the in vitro chromosomal aberration (CHL cell line) and in vitro sister chromatid exchange (CHL/IU cell line) assays.
Levofloxacin caused no impairment of fertility or reproduction in rats at oral doses as high as 360 mg/kg/day, at which systemic exposure was estimated to be 2,600 times that at the maximum recommended human ophthalmic dose.
Use In Specific Populations Pregnancy Pregnancy Category C Teratogenic Effects Levofloxacin at oral doses of 810 mg/kg/day in rats caused decreased fetal body weight and increased fetal mortality.
No teratogenic effect was observed when rabbits were dosed orally as high as 50 mg/kg/day, at which systemic exposure was estimated to be 250 times that observed at the maximum recommended human ophthalmic dose, or when dosed intravenously as high as 25 mg/kg/day, at which systemic exposure was estimated to be 120 times that observed at the maximum recommended human ophthalmic dose.
There are, however, no adequate and well-controlled studies in pregnant women.
Levofloxacinshould be used during pregnancy only if the potential benefit justifies the potential risk to thefetus.
Nursing Mothers Levofloxacin has not been measured in human milk.
Based on data from ofloxacin, it can be presumed that levofloxacin is excreted in human milk.
Caution should be exercised when IQUIX® is administered to a nursing mother.
Pediatric Use Safety and effectiveness in children below the age of six years have not been established.
Oral administration of systemic quinolones has been shown to cause arthropathy in immature animals.
There is no evidence that the ophthalmic administration of levofloxacin has any effect on weight bearing joints.
Geriatric Use No overall differences in safety or effectiveness have been observed between elderly and other adult patients.
|
More Medical Conditions
A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z
Medical Conditions Definitions Of The Day
- Aortic Coarctations ‐ Narrowing of the lumen of the aorta, caused by deformity of the…
- Gelada Baboons ‐ A genus of Old World monkeys of the subfamily CERCOPITHECINAE,…
- Detections, Signal (Psychology) ‐ Psychophysical technique that permits the estimation of the bias…
- Drug Toxicities ‐ Manifestations of the adverse effects of drugs administered therapeutically…
- Peptide Elongation Factor G ‐ Peptide Elongation Factor G catalyzes the translocation of peptidyl-tRNA…
- Systems, Vasomotor ‐ The neural systems which act on vascular smooth muscle to control…
- Platelet Activating Factor ‐ A phospholipid derivative formed by platelets, basophils, neutrophils,…
- Sialuria, Infantile Form ‐ Autosomal recessive neurodegenerative disorders caused by lysosomal…
- Spastic Paraparesis ‐ Mild or moderate loss of motor function accompanied by SPASTICITY…
- Cycles, Endometrial ‐ The period of the regularly recurring physiologic changes in…