Anthropometric Measurements as Predictors of Low Birth Weight Among Tanzanian Neonates: A Hospital-Based Study
November 7, 2025
Brand Name :
Lithostat
Synonyms :
acetohydroxamic acid
Class :
Antimicrobial
Dosage Forms & Strengths
Tablet
250mg
Indicated for chronic urinary tract infections:
Initial dose:12mg/kg/day orally divided every 6-8 hours on an empty stomach
Maintenance dose:250mg orally every 6-8 hours. Do not exceed 1.5g/day
Dose Adjustments
Renal impairment
The serum creatinine (SCr) levels in the blood determine the recommended frequency and amount of the medication to be taken. If the SCr level is between 1.8-2.5 mg/dL, the medication should be taken every 12 hours, with a maximum daily dose not exceeding 1 g. However, if the SCr level is more significant than 2.5 mg/dL, the medication is not recommended
Tablet
250mg
Indicated for chronic urinary tract infections:
Initial dose:10mg/kg/day orally divided every 6-8 hours on an empty stomach
Indicated for chronic urinary tract infections:
Initial dose:12mg/kg/day orally divided every 6-8 hours on an empty stomach
Maintenance dose:250mg orally every 6-8 hours. Do not exceed 1.5g/day
may increase the toxic effects of acetohydroxamic acid
Mechanism of action
acetohydroxamic acid (AHA) is a chemical that acts as an inhibitor of bacterial urease, an enzyme found in many urinary tract infections (UTIs) causing bacteria. By inhibiting urease, AHA interferes with the formation of urea and the subsequent breakdown of urine, thus leading to reduced bacterial growth and eventual clearance of UTIs
Spectrum
The spectrum of activity of AHA is narrow, meaning that it only affects a limited range of bacteria. It is effective against various bacterial species that cause UTIs, including Proteus mirabilis, Klebsiella pneumoniae, and Staphylococcus saprophyticus. However, it is not active against other common bacterial pathogens, such as Escherichia coli and Pseudomonas aeruginosa
Frequency defined:
>10%
Anorexia
Nausea
Anxiety
Depression
Hemolytic anemia
Mild headache
Vomiting
Confused
Involuntary quivering
<1%
Blood clot
Phlebitis
Alopecia
Macular rash
Contraindications
Caution
Pregnancy and breast-feeding: AHA is contraindicated in pregnant women as it may harm the fetus. Breast-feeding women should also avoid the use of AHA.
Hypersensitivity: AHA may cause allergic reactions in individuals who are hypersensitive to it.
Renal impairment: AHA is contraindicated in individuals with severe renal impairment as it can accumulate in the body and cause adverse effects.
Drug interactions: AHA may interact with other medications, particularly those that affect the renal system, and may increase the risk of toxicity.
Hemolytic anemia: AHA may cause hemolytic anemia in individuals with certain blood disorders
Pregnancy consideration: It is contraindicated in pregnant women as it may harm the fetus
Lactation: Excretion of the drug in human breast milk is unknown
Pregnancy category:
Category A: well-controlled and Satisfactory studies show no risk to the fetus in the first or later trimester.
Category B: there was no evidence of risk to the fetus in animal studies, and there were not enough studies on pregnant women.
Category C: there was evidence of risk of adverse effects in animal reproduction studies, and no adequate evidence in human studies must take care of potential risks in pregnant women.
Category D: adequate data available with sufficient evidence of human fetal risk from various platforms, but despite the potential risk, and used only in emergency cases for potential benefits.
Category X: Drugs listed in this category outweigh the risks over benefits. Hence these categories of drugs need to be avoided by pregnant women.
Category N: There is no data available for the drug under this category
Pharmacology
acetohydroxamic acid (AHA) is an inhibitor of bacterial urease, an enzyme in many urinary tract infections (UTIs) causing bacteria. By inhibiting urease, AHA reduces the formation of ammonia and subsequent bacterial growth, leading to the eventual clearance of UTIs
Pharmacodynamics
The pharmacodynamics of acetohydroxamic acid (AHA) involves the inhibition of the bacterial enzyme urease. Urease is an enzyme found in many bacteria that cause urinary tract infections (UTIs), and it helps to break down urea in the urine, leading to the formation of ammonia. The ammonia increases the pH of the urine, making it more alkaline and creating an environment favorable for bacterial growth.
AHA works by inhibiting urease’s activity, which reduces ammonia’s production and subsequent bacterial growth. This leads to a reduction in the number of bacteria causing UTIs and a subsequent improvement in symptoms
Pharmacokinetics
Absorption: AHA is rapidly absorbed from the gastrointestinal tract after oral administration.
Distribution: AHA is widely distributed in the body and can cross the blood-brain barrier.
Metabolism: AHA is rapidly metabolized in the liver and kidneys to form several inactive metabolites.
Elimination/Excretion: AHA and its metabolites are primarily eliminated in the urine
Administration
Generally, AHA is taken twice a day, with or without food. It is essential to follow the dosing instructions a healthcare professional provides and stay within the maximum recommended daily dose.
It is also important to note that AHA should be taken consistently, as missing doses may reduce its effectiveness. If a dose is missed, it should be taken as soon as possible. If it is close to the next dose, the missed dose should be skipped, and the next dose should be taken regularly
Patient information leaflet
Generic Name: acetohydroxamic acid
Pronounced: [ a-SEET-oh-HYE-drox-AM-ik-AS-id ]
Why do we use acetohydroxamic acid?
acetohydroxamic acid (AHA) treats urinary tract infections (UTIs) caused by bacteria that produce the enzyme urease. It is also used with antibiotics for treating chronic bacterial prostatitis and as an adjunctive treatment for bladder cancer.