Contraindications
AGEXA-OZ (Ofloxacin 200 mg & Ornidazole 500 mg) Tablet from AGEX LABORATORIES PVT LTD is contraindicated in those with known hypersensitivity to its ingredients, pregnant women, or those having possibilities of being pregnant, and in children. Breast feeding is to be avoided whilst on AGEXA-OZ treatment.

Hypersensitivity to ornidazole ( in AGEXA-OZ) or to other nitroimidazole derivatives.

Precautions & Warnings

AGEXA-OZ from Agex Laboratories is to be advocated with caution in severe nephropathy, convulsive disorders, known hyper sensitivity to quinolones and in elderly patients. It should be co-administered with caution along with nonsteroidal anti-inflammatory drugs, antacids, hematinics and anticoagulants.

Special Precautions and hepatic impairment. CNS diseases e.g. epilepsy or multiple sclerosis. May impair ability to drive or operate machinery, pregnancy and lactation.

Adverse Reactions

AGEXA-OZ may cause gastrointestinal intolerance, psychoneurologic symptoms and allergic reactions. It can rarely cause malaise, fever, palpitations, taste abnormality, convulsions, acute renal failure, jaundice, hematologic abnormalities, rhabdomyolysis, hypoglycemia in susceptible diabetics, tendon disorders and psychiatric symptoms such as confusion.

Ornidazole (in AGEXA-OZ ) can cause Somnolence, headache, nausea, vomiting, dizziness, tremor, rigidity, poor coordination, seizures, tiredness, vertigo, temporary loss of consciousness and signs of sensory or mixed peripheral neuropathy, taste disturbances, abnormal LFTs, skin reactions

 Dosage & Administration

Oral Administration
Adults:
AGEXA-OZ Tablet twice daily or as prescribed

Presentations
AGEXA-OZ Tablet: Alu Alu of 10s.