Minoz 100mg Tablet 10s
MRP: ₹345.00
Packaging
10 TAB
Composition
Minocycline 100mg
Company
Sun Pharma
MRP: ₹345.00
Packaging
10 TAB
Composition
Minocycline 100mg
Company
Sun Pharma
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Minocycline is used in certain bacterial infections such as pneumonia, acne and infections of the bladder, central nervous system, eye and prostate.
Oesophageal ulceration; vestibular disturbances e.g. dizziness or vertigo, tinnitus and decreased hearing; hyperpigmentation of the skin; SLE or lupus-like symptoms; GI disturbances; benign intracranial hypertension; abnormal LFTs, hyperbilirubinaemia or jaundice; teeth discolouration in children. Potentially Fatal: Hypersensitivity syndrome. Hepatitis or liver damage. Pneumonitis.
Oral absorption may be impaired by calcium-containing antacids and other divalent or trivalent cations. Decreases effectiveness of oral contraceptives. May increase plasma levels of lithium, theophylline. Pseudotumour cerebri may occur when used with isotretinoin. Additive facial pigmentation with ethinylestradiol. Potentially Fatal: May increase effects of oral anticoagulants.
Hypersensitivity to minocycline, other tetracyclines. Pregnancy and lactation.
Minocycline inhibits protein synthesis by binding to 30S and possibly 50S ribosomal subunits of susceptible bacteria. It is active against Streptococcus aureus, streptococci, Neisseria meningitidis, various enterobacteria, Acinetobacter, Bacteroides, Haemophilus and Nocardia spp, M. leprae and some mycobacteria. Absorption: Absorbed readily from the GI tract (oral); absorption not significantly affected by food and milk. Distribution: Protein-binding: 70-75%. Widely distributed in body tissues and fluids; high concentrations in hepatobiliary tract, lungs, sinuses, tonsils, tears, saliva, sputum. CSF (poor penetration). Crosses the placenta and enters breast milk. Metabolism: Some hepatic metabolism; converted to 9-hydroxyminocycline. Excretion: Via faeces (34%); via urine (5-10%). Elimination half-life: 11-26 hr; prolonged in renal impairment.
May cause photosensitivity; discontinue at the 1st signs of erythema. May impair ability to drive or operate machinery. Monitor renal, hepatic and haematologic functions during therapy. Hepatic and renal impairment. Children ≤8 yr. Oral forms should be taken with plenty of fluids with the patient in an upright position.
Take orally with food and water, as directed by your physician.
Keep in a cool, dry place away from sunlight and moisture.
This content is for educational purposes only. Please consult your doctor before use.
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Written by: SastiMedic Medical Team
Reviewed by: Registered Pharmacist