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Bekker OZ Oral Suspension

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Prescription Required

Marketer

Afive Pharma

Salt Composition

Ofloxacin (50mg) + Ornidazole (125mg)

Overview Bekker OZ Oral Suspension

Children's OZ Bekker oral suspension is an antibiotic combating various bacterial infections affecting the teeth, lungs, digestive system, and urinary/genital tracts. Administer this medication orally to your child, ideally at the same time each day, either before or after meals; if stomach upset occurs, give it with food. The typical dosage is twice daily, morning and evening. If vomiting occurs within 30 minutes, repeat the dose; however, avoid doubling if the next dose is due. Always adhere to your doctor's prescribed dosage, timing, and method, as these are tailored to the infection's severity, your child's age, and weight. Minor, transient side effects like nausea, vomiting, metallic taste, headache, appetite loss, abdominal discomfort, and mild rash may occur, usually resolving spontaneously. Persistent or bothersome side effects necessitate immediate consultation with your child's physician. Prior to treatment, inform your doctor of any allergies, heart conditions, liver problems, or kidney issues your child may have; a complete medical history is essential for appropriate dosage and treatment planning.

Uses of Bekker OZ Oral Suspension

Combating bacterial and parasitic infestations

Major Benefits of Bekker OZ Oral Suspension:

Administer this medication precisely as your physician directs, adhering to both the prescribed dosage and timeframe. Consult the product label for complete instructions prior to consumption. Use a measuring device for accurate dosing, and ingest orally. Ensure thorough shaking before each use. Bekker OZ Oral Suspension can be consumed with or without food; however, consistent timing is recommended.

Common Side effects of Bekker OZ Oral Suspension:

  • Weight loss
  • Nausea
  • Dizziness
  • Headache
  • Insomnia (difficulty in sleeping)
  • Vomiting
  • Itching
  • Vaginal inflammation
  • Diarrhea

How to use Bekker OZ Oral Suspension:

Administer this medication precisely as your physician directs, adhering to the prescribed dosage and timeframe. Consult the product label for complete instructions prior to ingestion. Use a measuring device for accurate dispensing and consume orally. Ensure thorough shaking before each use. Bekker OZ Oral Suspension can be ingested with or without food; however, consistent timing is recommended for optimal results.

How Bekker OZ Oral Suspension works:

Ofloxacin and ornidazole, the active components in Bekker OZ Oral Suspension, are antibiotics that disrupt bacterial DNA replication. This mechanism effectively eliminates infectious bacteria, halting their proliferation and preventing the development of antibiotic resistance.

SAFETY ADVICE

KidneyKidneyCAUTION

Individuals with impaired kidney function should use Bekker OZ Oral Suspension cautiously. Dosage modification of Bekker OZ Oral Suspension might be necessary. Physician consultation is advised.

LiverLiverCAUTION

Patients with liver impairment should use Bekker OZ Oral Suspension cautiously; dosage modification may be necessary. Physician consultation is advised.

What if you forget to take Bekker OZ Oral Suspension :

Remain calm. Administer the medication at your earliest convenience unless alternative instructions have been provided by your child's physician. If uncertain about the dosage, contact your doctor immediately; avoid doubling the dose to compensate for a missed one.

Facts to Know About Bekker OZ Oral Suspension

LabelValue
Addictive None.
Type of Treatment Digestive system

FAQs on Bekker OZ Oral Suspension

Concurrent use of Bekker OZ Oral Suspension and cough or cold medications may be problematic. A component of Bekker OZ Oral Suspension can react negatively with alcohol-based medications, such as some cough syrups, potentially leading to undesirable side effects. Always seek medical advice before administering any other medications to a child already taking Bekker OZ Oral Suspension.
While an additional dose of Bekker OZ Oral Suspension is unlikely to harm your child, avoid giving any medication in excess. Contact a physician immediately if you suspect an overdose. Administering more than the prescribed amount could result in adverse reactions including convulsions, shaking, intense headache, abrupt weakness, blood cell irregularities, and a rapid, erratic pulse. Seek urgent medical attention for your child should any of these signs appear.
Lack of improvement suggests the medication may be ineffective against the infecting bacteria. Consult your child's physician; they might prescribe a broader-spectrum antibiotic than Bekker OZ Oral Suspension. Alternatively, given that administration isn't always oral, your doctor may recommend intravenous treatment at the hospital.
Bekker OZ Oral Suspension may interact with other medications or substances. Inform your child's physician of all other medications your child is currently using prior to administering Bekker OZ Oral Suspension. Always consult your child's doctor before giving your child any medication.
Typically, antibiotics don't negatively interact with vaccine components or trigger adverse reactions in recently vaccinated children. Nevertheless, vaccination should be postponed for children receiving antibiotics until their illness resolves. Once your child is well, vaccination is appropriate.
Advise your physician if your child has a history of heart disease, inherited vascular disorders, convulsions, mental health conditions, diabetes, photosensitivity, muscle or nerve disorders, or rheumatoid arthritis. Bekker OZ Oral Suspension could potentially worsen these pre-existing conditions, leading to adverse effects.
Ofloxacin and Ornidazole, the active components in Bekker OZ Oral Suspension, combat harmful microorganisms responsible for infections. This combination therapy provides effective treatment of various infections.
Oral Bekker OZ Suspension is generally well-tolerated. However, some individuals may experience typical adverse reactions including nausea, vomiting, abdominal discomfort, vertigo, cephalalgia, xerostomia, and pyrosis, along with less frequent or infrequent side effects. Seek medical advice if any adverse effect persists.
Patients allergic to ofloxacin, ornidazole, or any quinolone or nitroimidazole antimicrobial should avoid Bekker OZ Oral Suspension, as its use poses a risk.
Exceeding the prescribed dosage of Bekker OZ Oral Suspension elevates the likelihood of adverse reactions. Should your symptoms worsen despite adhering to the recommended dose, seek medical advice for reassessment.
Consult your physician if your condition hasn't improved after completing the prescribed medication. Similarly, report any worsening of symptoms during treatment.
Discontinue use of Bekker OZ Oral Suspension is not advised; finish the prescribed treatment, regardless of symptom improvement. Complete eradication of the infection may require the full course of medication.
Administer Bekker OZ Oral Suspension upon recollection. Refrain from taking it if the next scheduled dose is imminent. Avoid doubling the dose to compensate for a missed one.
Refrain from consuming alcohol as it could worsen the drowsiness and dizziness induced by Bekker OZ Oral Suspension. Seek your physician's advice if you have any uncertainty regarding the medication's effects.
Store the medication in its original, tightly sealed container. Follow the storage instructions provided on the packaging. Discard any remaining medication. Prevent access by children, pets, and others.
Ofloxacin and Ornidazole, the components of Bekker OZ Oral Suspension, are antimicrobial agents. This combination combats harmful microorganisms responsible for infections, thus providing effective treatment.
Oral Bekker OZ Suspension is generally well-tolerated. However, some individuals may experience typical adverse reactions including nausea, vomiting, abdominal discomfort, vertigo, cephalalgia, xerostomia, and pyrosis, along with less frequent or infrequent side effects. Seek medical advice should any issue persist during treatment.
Patients allergic to ofloxacin, ornidazole, or any quinolone or nitroimidazole antimicrobial should avoid Bekker OZ Oral Suspension, as its use poses a risk.
Exceeding the prescribed dosage of Bekker OZ Oral Suspension elevates the likelihood of adverse reactions. Should your symptoms worsen despite adhering to the recommended dose, seek medical advice for reassessment.
Consult your physician if your condition doesn't improve after completing the prescribed medication regimen. Similarly, report any worsening of symptoms during treatment.
Discontinue Bekker OZ Oral Suspension only upon completion of the prescribed regimen. Continue taking the medication as directed, even if symptoms subside; feeling better doesn't necessarily indicate complete eradication of the infection.
Administer Bekker OZ Oral Suspension upon recollection. However, omit the dose if the next scheduled administration is imminent. Avoid doubling the dose to compensate for a missed one.
Refrain from consuming alcohol as it could worsen the drowsiness and dizziness that Bekker OZ Oral Suspension may induce. Seek your physician's advice if you have any uncertainties regarding the drug's impact.
Retain this medication in its original, sealed container. Follow the storage instructions provided on the packaging. Discard any remaining medication. Ensure the medicine remains inaccessible to children, pets, and others.
Bekker OZ Oral Suspension
45
MRP 55
18% off