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Levosina (Levofloxacin)

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Levosina is a fluoroquinolone antibacterial agent with a broad spectrum of activity against Gram-positive and Gram-negative bacteria and atypical respiratory pathogens. It is active against both penicillin-susceptible and penicillin-resistant Streptococcus pneumoniae.

Other names for this medication:
Armolev, Floximax, Iquix, Leoflox, Letab, Levofloxacina, Levofloxacino, Levofloxacinum, Levonidin, Levoprolin, Levoquinol, Levotac, Levovid, Levoxa, Levoxal, Lovicin, Nevotek, Nivoloc, Ovelquin, Potant, Quinix, Rinvox, Tavanic, Teraquin, Tevox, Urilev

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Also known as: Levofloxacin


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


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


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 Levosina 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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Many genes related to the circadian rhythm, especially those involved in phase shifts induced by different environmental stimuli, still remain enigmatic. Evidence for a single pedigree source of the hyperkalemic periodic paralysis susceptibility gene in quarter horses. Clinical characteristics of coronary heart disease in women: emphasis on gender differences. We consider a noncooperative interaction among a large population of mobiles that interfere with each other through many local interactions. The authors think that not all but some such children could develop their ability to operate powered wheelchairs and might expand their knowledge about the circumstances and interests in them. The expression of the CUP1 gene is induced at the level of transcription by copper via cis-dominant upstream control sequences which are tandemly repeated. However, further investigations are necessary to verify primacy of the calvaria in flagyl 500 mg capsule this model.

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