Medication info

Lometec Tablet (Lomefloxacin Hydrochloride)

Prescription medicationExpired
Ingredient · strength
Lomefloxacin Hydrochloride›Strength being verified
Manufacturer / importer
Austin Pharma Co., Ltd.
Appearance
White oval film-coated tablet
Packaging
30 tablets/bottle, 100 tablets/bottle
Approval status
Expired

MFDS item code 200501795 · Notified 2005.11.04

This product's status changed to Expired on 2023.04.01. It may no longer be sold, so consult a doctor or pharmacist before taking it.

Summary

Main use
Treatment of genitourinary, respiratory, and intestinal infections, skin infections, and eye, ear, and dental infections
Who uses it
Adults
Adult dosage
(Tablets) 1. Administer lomefloxacin 100 ~ 200 mg orally 2 ~ 3 times daily. 2. However, for acute exacerbations of chronic obstructive pulmonary disease, including chronic bronchitis, the usual adult dose is 400 mg of this drug orally once daily, during or without meals. The duration of administration varies depending on the severity of the infection, but is usually up to 14 days; treatment should continue for at least 2 days after the symptoms of infection have resolved. 3. Patients with renal impairment 1) Patients with creatinine clearance below 30 mL per minute should receive an initial dose of 400 mg of this drug once, followed by 200 mg once daily starting the next day. 2) Patients on hemodialysis should receive an initial dose of 400 mg of this drug, followed by 200 mg once daily starting the next day. 3) Dose adjustment is not necessary in patients with hepatic impairment; adjust the dose according to renal function.

Ingredients

Manufacturer
Austin Pharma Co., Ltd.

Efficacy & effects

Treatment of genitourinary, respiratory, and intestinal infections, skin infections, and eye, ear, and dental infections

  • Folliculitis
  • pustular acne
  • boils
  • large boils
  • superficial soft tissue infections
  • soft tissue infections
  • lymphangitis
  • paronychia
  • pyogenic paronychia
  • subcutaneous abscess
  • pyogenic hidradenitis
  • necrotizing acne
View approved original text

This medication is effective against various bacterial infections. It is used for skin and soft tissue infections such as folliculitis, pustular acne, and boils, as well as respiratory infections like chronic bronchitis, community-acquired pneumonia, and lung abscess. It is also effective for urinary tract infections including acute uncomplicated pyelonephritis, cystitis, bacterial prostatitis, and gonococcal urethritis. Additionally, it is applicable for intestinal infections such as gastroenteritis and bacterial dysentery, as well as infections in various areas like pelvic inflammatory disease, ocular infections, otitis media, sinusitis, and periodontal diseases. However, this drug should be used cautiously when there are no alternative treatment options due to the risk of severe adverse reactions. Overall, this medication is utilized for the treatment of bacterial infections in multiple areas.

Dosage and Administration

Adult dosage

(Tablets) 1. Administer lomefloxacin 100 ~ 200 mg orally 2 ~ 3 times daily. 2. However, for acute exacerbations of chronic obstructive pulmonary disease, including chronic bronchitis, the usual adult dose is 400 mg of this drug orally once daily, during or without meals. The duration of administration varies depending on the severity of the infection, but is usually up to 14 days; treatment should continue for at least 2 days after the symptoms of infection have resolved. 3. Patients with renal impairment 1) Patients with creatinine clearance below 30 mL per minute should receive an initial dose of 400 mg of this drug once, followed by 200 mg once daily starting the next day. 2) Patients on hemodialysis should receive an initial dose of 400 mg of this drug, followed by 200 mg once daily starting the next day. 3) Dose adjustment is not necessary in patients with hepatic impairment; adjust the dose according to renal function.

Precautions

This medication is a fluoroquinolone antibiotic used for the treatment of specific bacterial infections. Caution should be taken when using this medication as serious side effects such as tendonitis, tendon rupture, peripheral neuropathy, central nervous system disorders, and exacerbation of myasthenia gravis may occur. If any of these symptoms arise, discontinue the medication immediately and consult a healthcare professional. This drug should not be used in patients with a history of myasthenia gravis, and should only be used when no other treatment alternatives are available. Especially in elderly patients, those with impaired kidney function, solid organ transplant recipients, and those taking corticosteroids concurrently, the risk of tendon rupture may increase, and concomitant use should be avoided. If symptoms of tendonitis or tendon rupture occur, rest and avoid exercise, and if symptoms are severe, discontinue the medication immediately. This drug is not administered to patients who have a hypersensitivity to quinolone antibiotics, children under 18 who are still growing, pregnant or nursing women, or those who have previously experienced tendonitis or rupture from this drug. Patients with a history of seizures or convulsions, severe renal impairment, elderly patients, or those with a history or family history of aortic aneurysm or aortic dissection should be given this medication with caution. During administration, various side effects such as anaphylactic shock, skin rash, photosensitivity reactions, abnormal renal and liver function, gastrointestinal symptoms, central nervous system abnormalities, respiratory issues, blood abnormalities, central nervous system stimulation symptoms, cardiovascular issues, musculoskeletal issues, tinnitus, genital issues, and systemic fatigue may occur; if any of these adverse effects are noticed, consult a healthcare professional immediately. Additionally, during treatment with this medication, strong sunlight or artificial UV exposure should be avoided, and care should be taken to avoid dizziness while driving or operating machinery. Diabetics who require blood glucose control should closely monitor changes in blood sugar levels and seek immediate treatment if hypoglycemic symptoms occur. This medication may interact with certain drugs, so if any other medications are being taken, it is important to inform healthcare providers. Pregnant or nursing women should not use this medication and should consult a doctor if necessary. In the case of an overdose, notify healthcare professionals immediately and receive appropriate treatment, as blood dialysis or peritoneal dialysis may not significantly aid in drug removal. Caution is needed to avoid potential skin abnormalities due to UV exposure during long-term use.

Side effects

  • Tendinitis
  • tendon rupture
  • peripheral neuropathy
  • central nervous system effects
  • exacerbation of myasthenia gravis
  • anaphylactic shock
  • anaphylactoid reaction
  • rash
  • urticaria
  • erythema
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  • pruritus
  • edema
  • angioedema
  • conjunctival congestion
  • vesicles
  • erythema
  • photosensitivity reactions
  • exfoliative dermatitis
  • hyperpigmentation
  • mucous membrane syndrome
  • toxic epidermal necrolysis
  • hypokalemia
  • elevated BUN
  • elevated serum creatinine
  • acute renal failure
  • elevated AST
  • elevated ALT
  • elevated ALP
  • elevated serum bilirubin
  • gastrointestinal inflammation
  • oral candidiasis
  • constipation
  • diarrhea
  • loss of appetite
  • dyspepsia
  • vomiting
  • nausea
  • abdominal pain
  • stomatitis
  • angular cheilitis
  • oral psoriasis
  • gastric discomfort
  • abdominal distension
  • gastrointestinal disorders
  • dry mouth
  • blood in stool
  • nervousness
  • drowsiness
  • agitation
  • changes in appetite
  • confusion
  • personality loss
  • depression
  • delirium
  • hallucinations
  • paranoia
  • restlessness
  • loss of orientation
  • attention deficit
  • memory impairment
  • headache
  • dizziness
  • insomnia
  • tremors
  • nightmares
  • dyspnea
  • respiratory infections
  • nosebleeds
  • influenza
  • other respiratory disorders
  • increased monocytes
  • elevated ESR
  • decreased white blood cells
  • decreased platelets
  • increased eosinophils
  • decreased red blood cells
  • decreased hemoglobin
  • decreased hematocrit
  • hemolytic anemia
  • sensory disturbances
  • seizures
  • sweating
  • flushing
  • edema
  • hypertension
  • lethargy
  • tachycardia
  • arrhythmia
  • ectopic beats
  • phlebitis
  • palpitations
  • angina
  • cerebral thrombosis
  • QT prolongation
  • ventricular tachycardia
  • leg cramps
  • arthralgia
  • myalgia
  • weakness
  • elevated creatine kinase
  • elevated myoglobin
  • rhabdomyolysis
  • tinnitus
  • vaginitis
  • vaginal discharge
  • intermenstrual bleeding
  • vaginal candidiasis
  • orchitis
  • fatigue
  • abdominal pain
  • debility
  • anxiety
  • chilliness in the face or hands
  • malaise
  • sensation of heat
  • lymphatic edema
  • loss of taste
  • visual disturbances
  • gout
  • thirst
  • arching of the soft palate
  • hypoglycemia
  • polyuria
  • laryngeal and pulmonary edema
  • aortic aneurysm
  • aortic dissection
  • valvular regurgitation
  • valvular insufficiency

Not everyone experiences these, and they can vary from person to person.

Storage

This medication should be stored in a tightly closed container that protects from light, and it is best to keep it at room temperature between 1 to 30 degrees Celsius. Storing it this way helps maintain the effectiveness of the drug and prevents degradation.

Appearance and packaging

Appearance

White oval film-coated tablet

Package unit

30 tablets/bottle, 100 tablets/bottle

Same-ingredient medicines

Even with the same ingredient, strength, dosage form and how it is taken can differ.

Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.

Questions about this medicine

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This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.