Emrok Injection 100 ml
₹2689.6*
MRP ₹3280
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₹2788*
MRP ₹3280
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Emrok Injection 100 ml belongs to the group of medicines called antibiotics used to treat acute bacterial skin and skin structure infections, including diabetic foot infections and bacteraemia (presence of viable bacteria in the bloodstream). Emrok Injection 100 ml should only be used to treat bacterial infections and not viral infections.
Emrok Injection 100 ml contains 'levonadifloxacin', which works by inhibiting DNA gyrase and topoisomerase IV, which are essential for DNA replication, transcription, and repair. Thereby, Emrok Injection 100 ml helps treat bacterial skin and skin structure infections.
In some cases, Emrok Injection 100 ml may cause side effects such as gastrointestinal disorders and injection site reactions. Most of these side effects do not require medical attention and will gradually resolve over time. However, you are advised to speak to a healthcare professional if these side effects persist or worsen.
Consult your doctor if you are pregnant or breastfeeding. The safety and effectiveness of Emrok Injection 100 ml in children below 18 years have not been established. Keep your doctor informed about your health condition and medications to rule out any interactions/side effects.
Emrok Injection 100 ml belongs to the group of medicines called antibiotics used to treat acute bacterial skin and skin structure infections, including diabetic foot infections and bacteraemia. Emrok Injection 100 ml contains 'levonadifloxacin', which works by inhibiting DNA gyrase and topoisomerase IV, which are essential for DNA replication, transcription, and repair. Emrok Injection 100 ml is a broad-spectrum antibiotic with bactericidal activity against gram-positive and gram-negative organisms.
Do not take Emrok Injection 100 ml if you are allergic to any of its components. Consult your doctor if you are pregnant or breastfeeding. Tell your doctor if you have mental-health-related problems, diabetes, myasthenia gravis, tendinitis, tendon rupture, peripheral neuropathy, heart, kidney or liver problems. Inform your doctor if you experience convulsions, dizziness, lightheadedness, persistent headache with or without blurred vision; symptoms of muscle weakness, peripheral neuropathy (pain, burning, tingling, numbness and/or weakness of feet or hands), tendon rupture/tendinitis (pain, swelling, or inflammation of a tendon or weakness) or respiratory difficulties.
Drug-Drug Interaction: No interactions found/established.
Drug-Food Interaction: No interactions found/established.
Drug-Disease Interaction: No interactions found/established.
Bacterial skin and skin structure infections: Bacterial skin and skin structure infections, also known as skin and soft tissue infections, are infections associated with skin and soft tissues (mucous membrane and loose connective tissue). Symptoms include swelling, rashes, itching, pus, pain, and redness.
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Alcohol
Caution
It is not known if alcohol interacts with Emrok Injection 100 ml. Please consult your doctor if you have any concerns.
Pregnancy
Caution
Emrok Injection 100 ml belongs to pregnancy category C. Inform your doctor if you are pregnant before receiving Emrok Injection 100 ml. Your doctor will prescribe Emrok Injection 100 ml only if the benefits outweigh the risks.
Breast Feeding
Caution
It is not known if Emrok Injection 100 ml passes into breastmilk. So, inform your doctor if you are breastfeeding before receiving Emrok Injection 100 ml.
Driving
Caution
No studies on the effect of Emrok Injection 100 ml on the ability to drive have been conducted. If you have any symptoms that impair your ability to concentrate or respond, do not drive.
Liver
Caution
No dose adjustment is required. However, if you have liver problems, inform your doctor before taking Emrok Injection 100 ml.
Kidney
Caution
Studies of Emrok Injection 100 ml in people with renal impairment have not been conducted. Hence, if you have kidney problems, inform your doctor before taking Emrok Injection 100 ml.
Children
Unsafe
Emrok Injection 100 ml is not recommended for use in children below 18 years as the safety and effectiveness have not been established.
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