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Active Pharma Ingredients / 07 Sep 2026

BALOFLOXACIN

Generic Name: BALOFLOXACIN

ABSTRACT -

Balofloxacin is a fluoroquinolone antibacterial. Current status: marketed in selected countries; not a universal FDA/EMA standard product. Mechanistic summary: inhibits bacterial DNA gyrase and topoisomerase IV. This document is for structured API information only and is not a prescribing guide. Clinical use, if any, must follow the approved local label, institutional protocol, and specialist medical judgment.

DOSAGE-

  • Use only the approved local label or trial protocol for dose, route, duration, and monitoring.
  • Adjust dosing for renal/hepatic impairment, age, body weight, and interacting medicines where class-relevant.
  • Do not self-administer or substitute products without prescriber review.

SIDE EFFECTS-

Possible side effects and safety concerns include:

  • Headache, dizziness, fatigue, or gastrointestinal discomfort
  • Laboratory abnormalities depending on class and dose
  • Class-specific effects such as infection risk, QT effects, CNS effects, or liver-enzyme changes where applicable
  • Serious adverse reactions are possible and require medical review

ALLERGIC REACTIONS -

Hypersensitivity to Balofloxacin or related products may occur. Symptoms may include:

  • Urticaria, generalized rash, itching, flushing, or fever
  • Facial, lip, tongue, or throat swelling
  • Wheezing, chest tightness, shortness of breath, dizziness, or collapse
  • Anaphylaxis requiring emergency treatment

Important: patients with suspected allergy to Balofloxacin should seek immediate medical attention and inform future healthcare providers.

DRUG INTERACTIONS-

Balofloxacin may interact with medicines, biologics, vaccines, supplements, procedures, or clinical conditions. Caution is needed with:

  • CYP/P-gp modulators may alter exposure when metabolism is pathway-dependent.
  • Other agents with overlapping toxicity require caution.
  • Live vaccines, immunosuppressants, anticoagulants, CNS depressants, QT-prolonging drugs, or hormonal therapies may matter depending on the drug class.

Patients should provide a complete medicine list, including prescription drugs, over-the-counter products, herbal medicines, vaccines, and supplements.

PREAUTIONS–

  • Confirm indication, dose, renal/hepatic status, pregnancy status, and contraindications before use.
  • Monitor class-specific safety parameters such as CBC, liver enzymes, ECG, blood pressure, infection signs, or endocrine markers.
  • Use only according to an approved local label or formal clinical-trial protocol.

WARNINGS –

  • Do not use without qualified medical supervision, approved labeling, or a formal clinical-trial protocol.
  • Keep out of reach of children.

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