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Voleflok (Levofloxacin)

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Voleflok is used to treat a variety of bacterial infections. This medication belongs to a class of drugs known as quinolone antibiotics. It works by stopping the growth of bacteria. This antibiotic treats only bacterial infections.

Other names for this medication:
Bacnil, Cravit, Farlev, Floxator, Lailixin, Lebel, Leflokin, Letab, Levogen, Levoking, Levolacin, Levonidin, Levoxin, Medibiox, Neumoflox, Ovelquin, Proxime, Quinix, Quinobiot, Quinolev, Reskuin, Resquin, Ultraquin, Voleflok, Zenilev

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Also known as: Levofloxacin


Generic Voleflok 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 Voleflok acts by eliminating bacteria. It is fluoroquinolone. Generic name of Generic Voleflok is Levofloxacin. Voleflok is also known as Levofloxacin, Levotab, Levotas, Tavanic, Gatigol, Lebact, Terlev, Cravit, Levox, Levores. Brand name of Generic Voleflok is Voleflok.


You should take it by mouth. The treatment can be resulting after 7-14 days or 6 weeks. Take Generic Voleflok once a day with water. Do not crush or chew it. Do not stop taking Generic Voleflok suddenly.


Overdose of the drug should be strictly avoided and if anyone has accidentally taken the overdose of the drug, then the victim should be provided with emergency medical help. Overdose victim can also consult to their local poison helpline. Some of the overdose symptoms include loss of coordination, drooping eyelids, weakness, decreased activity, trouble breathing, sweating, tremors, or seizure.

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The most common side effects associated with Voleflok 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.


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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To evaluate feasibility of inhibiting coxsackievirus B3 (CVB3) infection at cellular, protein and gene levels by using small interfering RNA (siRNA). The hyperpermeability was corrected with bisindolylmaleimide and the selective PKCbeta inhibitor hispidin. Less than one quarter of the health care professionals and medical students knew the cleocin drug interaction importance of paternal family history in the evaluation for hereditary breast cancer. Differential requirement of unfolded protein response pathway for calreticulin expression in Caenorhabditis elegans. Vertebral osteomyelitis presenting as exudative pleural effusion. We report two cases of cutaneous primary melanoma associated with PEH and discuss differential diagnoses and potential role of p53 and bcl-2 in the pathogenesis of PEH. Imatinib resistance or intolerance frequently depends on the re-emergence of Bcr-Abl kinase activity, but can also indicate Bcr-Abl-independent disease progression. Using an appropriate statistical modeling framework, for a given microorganism, the doubling time has been estimated for each individual colony, as well as its variability between colonies, both within and between agar plates.

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