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Leflokin (Levofloxacin)
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Leflokin

Leflokin is an antibiotic. It is used orally to treat different types of bacterial infections of the throat, lungs, ears, nose, urinary tract, and skin. Leflokin is also used with other medications to stop the growth and kill Helicobacter pylori bacteria that cause stomach ulcer(s). It is not effective against infections caused by viruses or fungus.

Other names for this medication:
Armolev, Auxxil, Corvox, Farlev, Floximax, Lailixin, Laiwoxing, Ledric, Lefex, Leflumax, Lefoxin, Levocin, Levocine, Levonix, Levoproxol, Levox, Levoxacin, Levunid, Livacin, Lovequin, Loxof, Mosardal, Nevotek, Oftaquix, Ovelquin, Potant, Prolecin, Quinolev, Quixin, Resquin, Septibiotic, Tavaloxx, Tavanic, Trevox, Ultraquin, Voflaxin, Voleflok, Volequin, Zidalev

Similar Products:
Terramycin, Myambutol, Avelox, Biaxin, Sumycin

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Also known as: Levofloxacin

Description

Generic Leflokin is a perfect remedy. Its target is to struggle against infections such as chronic bronchitis, and sinus, urinary tract, pneumonia, kidney, and skin infections. Generic Leflokin acts by eliminating bacteria. It is fluoroquinolone. Generic name of Generic Leflokin is Levofloxacin. Leflokin is also known as Levofloxacin, Levotab, Levotas, Tavanic, Gatigol, Lebact, Terlev, Cravit, Levox, Levores. Brand name of Generic Leflokin is Leflokin.

Dosage

The usual dose of Leflokin Tablets or Oral Solution is 250 mg, 500 mg, or 750 mg administered orally every 24 hours, as indicated by infection and described in Table 1. The usual dose of Leflokin Injection is 250 mg or 500 mg administered by slow infusion over 60 minutes every 24 hours or 750 mg administered by slow infusion over 90 minutes every 24 hours.

Overdose

If you overdose Generic Leflokin and you don't feel good you should visit your doctor or health care provider immediately. Symptoms of Generic Leflokin overdosage: poor coordination, tremors, seizures, collapse, breathlessness, lack of movement.

Storage

Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F) away from moisture and heat. Keep in a tightly closed container. Throw away any unused medicine after the expiration date. Keep out of the reach of children.

Side effects

The most common side effects associated with Leflokin are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.

Contraindications

Risk of tendinitis and tendon rupture is increased. This risk is further increased in older patients usually over 60 years of age, in patients taking corticosteroids, and in patients with kidney, heart and lung transplants. Discontinue if pain or inflammation in a tendon occurs.

Anaphylactic reactions and allergic skin reactions, serious, occasionally fatal, may occur after first dose.

Hematologic (including agranulocytosis, thrombocytopenia), and renal toxicities may occur after multiple doses.

Hepatotoxicity: Severe, and sometimes fatal, hepatoxicity has been reported. Discontinue immediately if signs and symptoms of hepatitis occur.

Central nervous system effects, including convulsions, anxiety, confusion, depression, and insomnia may occur after the first dose. Use with caution in patients with known or suspected disorders that may predispose them to seizures or lower the seizure threshold.

Clostridium difficile-associated colitis: evaluate if diarrhea occurs.

Peripheral neuropathy: discontinue if symptoms occur in order to prevent irreversibility.

Prolongation of the QT interval and isolated cases of torsade de pointes have been reported. Avoid use in patients with known prolongation, those with hypokalemia, and with other drugs that prolong the QT interval.

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Separation and reconstitution of regulatory and catalytic components of heart adenylate cyclase. Cutaneous involvement in anaplastic large cell lymphoma may be in the form of primary cutaneous disease (primary cutaneous anaplastic large cell lymphoma) or secondary to involvement by systemic disease (systemic anaplastic large cell lymphoma). Rituximab plus cladribine with or without cyclophosphamide in patients with relapsed or refractory chronic lymphocytic leukemia. Based on these considerations the value of an MR study is discussed for each valvular lesion. In this study, data obtained in patients with thoracic myelopathy caused by degenerative processes of the spine were retrospectively analyzed to clarify the surgical outcomes and to examine the various factors affecting the postoperative improvement. We have investigated the effects of this antagonist on arginine-stimulated glucagon and insulin release in batch incubations of isolated rat islets, perifused isolated rat islets, and isolated perfused rat pancreas. Higher antiviral response of RIG-I through enhancing RIG-I/MAVS-mediated signaling by its long insertion variant in zebrafish. A major product of PARP degradation of about 89 kDa was found in the samples taken from the infarcted and penumbra areas. The number of states using legislation as a policy lever to promote EBPs was unchanged.

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