CYCLOSERINE

CYCLOSERINE Uses, Dosage, Side Effects, Food Interaction and all others data.

Antibiotic substance produced by Streptomyces garyphalus.

CYCLOSERINE, a broad-spectrum antibiotic, may be bactericidal or bacteriostatic, depending on its concentration at the site of infection and the susceptibility of the organism. CYCLOSERINE works by blocking the formation of these peptidoglycans. By doing this the walls of the bacteria become weak and it results in the death of the bacteria

Trade Name CYCLOSERINE
Availability Prescription only
Generic Cycloserine
Cycloserine Other Names alpha-Cycloserine, Cicloserina, cyclo-D-Serine, Cycloserine, Cyclosérine, Cycloserinum, D-Cycloserine, Orientomycin
Related Drugs prednisone, ciprofloxacin, levofloxacin, Levaquin, rifampin, Deltasone, Sterapred, Prednicot
Weight 250mg
Type Oral capsule
Formula C3H6N2O2
Weight Average: 102.0919
Monoisotopic: 102.042927446
Groups Approved
Therapeutic Class
Manufacturer King Pharmaceuticals Ltd
Available Country United Kingdom, United States
Last Updated: September 19, 2023 at 7:00 am
CYCLOSERINE
CYCLOSERINE

Uses

CYCLOSERINE is a broad-spectrum antibiotic used in the treatment of tuberculosis and certain urinary tract infections (UTI).

Used in combination with up to 5 other drugs as a treatment for Mycobacterium avium complex (MAC) and is also used to treat tuberculosis (TB).

CYCLOSERINE is also used to associated treatment for these conditions: Refractory Tuberculosis, Refractory Urinary Tract Infection

How CYCLOSERINE works

CYCLOSERINE is an analog of the amino acid D-alanine. It interferes with an early step in bacterial cell wall synthesis in the cytoplasm by competitive inhibition of two enzymes, L-alanine racemase, which forms D-alanine from L-alanine, and D-alanylalanine synthetase, which incorporates D-alanine into the pentapeptide necessary for peptidoglycan formation and bacterial cell wall synthesis.

Toxicity

Oral LD50 in mouse is 5290 mg/kg, and in rat is over 5000 mg/kg. Symptoms of a cycloserine overdose include drowsiness, confusion, headache, dizziness, irritability, numbness and tingling, difficulty speaking, paralysis, abnormal behavior, seizures, and unconsciousness.

Food Interaction

  • Do not take with or immediately after a high-fat meal. High-fat meals may reduce the rate of absorption; however, the impact on the extent of absorption is unknown.

[Major] GENERALLY AVOID: Coadministration with alcohol may potentiate some of the central nervous system adverse effects of cycloserine and its prodrug, terizidone.

These effects may include dizziness, drowsiness, depression, anxiety, psychoses, memory impairment, confusion, and convulsions.

MANAGEMENT: Patients should be advised to avoid the consumption of alcohol during treatment with cycloserine or terizidone.

The use of these medications is contraindicated in patients with chronic alcohol consumption or alcoholism.

MONITOR CLOSELY: Coadministration with caffeine may potentiate some of the central nervous system adverse effects of cycloserine and its prodrug, terizidone.

These effects may include insomnia, excitability, irritability, anxiety, tremor, psychoses, and convulsions.

MANAGEMENT: Caution is advised when cycloserine or terizidone is used with caffeine.

Consumption of certain beverages or stimulants with very high caffeine levels should be avoided as a precautionary measure.

CYCLOSERINE Disease Interaction

Major: colitis, CNS toxicity, renal dysfunction

Elimination Route

Rapidly and almost completely absorbed (70 to 90%) from the gastrointestinal tract following oral administration.

Half Life

Half-life in patients with normal renal function is 10 hours, and is prolonged in patients with impaired renal function.

Innovators Monograph

You find simplified version here CYCLOSERINE

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http://classyfire.wishartlab.com/tax_nodes/C0002211
http://classyfire.wishartlab.com/tax_nodes/C0004140
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*** Taking medicines without doctor's advice can cause long-term problems.
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