Isoniazid
๐ About
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- ๐ Most active first-line drug for treating tuberculosis (TB).
- โก Potent enzyme inhibitor.
โ๏ธ Action
- ๐ฆ Bactericidal โ inhibits synthesis of mycolic acids, essential for mycobacterial cell walls.
- ๐ Well absorbed, widely distributed (including CSF).
๐งช Properties
- ๐ Structurally similar to pyridoxine (vitamin B6).
- ๐ง Crosses bloodโbrain barrier, good CSF penetration.
- ๐งฌ Inactivated by hepatic acetylation (genetically variable).
๐ Indications
- ๐ฅ First-line treatment of tuberculosis (part of combination therapy).
๐ Interactions
- โฑ๏ธ Pharmacogenetics:
โข Rapid acetylators โ โ drug levels, tยฝ ~1 hr.
โข Slow acetylators โ โ drug levels, tยฝ ~3 hr โ more toxicity.
- โ ๏ธ Increases toxicity of phenytoin, carbamazepine, and warfarin.
โ ๏ธ Cautions
- ๐ซ Use with caution in porphyria.
โ Contraindications
- ๐งช Significant liver disease.
- ๐ซ Hypersensitivity to isoniazid.
๐ฅ Side Effects
- ๐ก๏ธ Rash, fever, drug-induced lupus.
- ๐ง Neuro: peripheral neuropathy (more common in slow acetylators), memory loss, psychosis, delirium, seizures, optic neuritis (rare).
- ๐ฉธ Haematological: agranulocytosis (rare).
- ๐งช Hepatitis: anorexia, nausea, vomiting, RUQ pain โ can be fatal โ stop drug immediately if suspected.
โก Seizures
- If due to isoniazid toxicity โ requires high-dose pyridoxine (vitamin B6).
- ๐ Always seek urgent expert help.
๐ Adult Dose
- ๐ Standard: 3โ5 mg/kg/day (usually 300 mg PO OD).
- ๐ Larger doses may be required in resistant cases (specialist advice).
- ๐ฝ๏ธ Take on an empty stomach for best absorption.
- ๐ Pyridoxine 10โ20 mg daily co-prescribed to prevent neuropathy.
- ๐งช Monitor FBC and LFTs during therapy.