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Cravox (Levofloxacin)

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Cravox is a Tablet manufactured by Cipla. It is commonly used for the diagnosis or treatment of Bacterial infections, bronchitis, gonorrhea, endocarditis, soft tissue, ear infection. It has some side effects such as Rash, Vaginal itching, Vaginal discharge, Vomiting. The salts Amoxicillin (500mg) are involved in the preparation of Cravox.

Other names for this medication:
Acquire, Anlev, Cinacol, Elequine, Exolev, Floxator, Floximax, Laiwoxing, Lebel, Leflokin, Leflox, Lefoxin, Levin, Levobact, Levocin, Levof, Levoflox, Levofloxacina, Levofloxacino, Levomac, Levomax, Levoproxol, Levoquin, Levoquinox, Levotac, Levovid, Levox, Levoxa, Levunid, Lexacin, Locin, Neumoflox, Nufalev, Oftaquix, Olcin, Ovelquin, Priflox, Prixar, Proxime, Quantrum, Quixin, Reskuin, Septibiotic, Teraquin, Uniflox, Yaxinbituo, Zidalev

Similar Products:
Cefixime, Chloromycetin, Cleocin, Suprax, Amoxil, Rulide, Levaquin, Biaxin, Terramycin

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Also known as: Levofloxacin


To reduce the development of drug-resistant bacteria and maintain the effectiveness of Cravox and other antibacterial drugs, Cravox should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy.

Cravox Tablets/Injection and Oral Solution are indicated for the treatment of adults (≥18 years of age) with mild, moderate, and severe infections caused by susceptible strains of the designated microorganisms in the conditions listed in this section. Cravox Injection is indicated when intravenous administration offers a route of administration advantageous to the patient (e.g., patient cannot tolerate an oral dosage form).


The usual dose of Cravox 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 Cravox 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 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.

Side effects

The most common side effects associated with Cravox 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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Complete coding sequences of European brown hare syndrome virus (EBHSV) strains isolated in 1982 in Sweden. Monospecific antiserum was prepared against the 27 and 31 kDa proteins and results indicate that they are immunogenic and share common epitopes. In the second alternation, tenseness of the stem vowel determines backness of the suffix vowel. The cellular localization of the cholecystokinin 2 (gastrin) receptor in the stomach. These fragmentation rules were implemented to analyze phenolic compounds in the fruits of F. One of the causes of failure after unicompartmental knee arthroplasty (UKA) for varus osteoarthritis is the progression of osteoarthritis in the lateral compartment. Thus, stem-loop III appears to confer a specific function to SL2 RNA. (Myxosporea, Sphaerosporidae), with emendation of the genus Sphaerospora. Dermatologic adverse effects of antiretroviral therapy: recognition and management.

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