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Brand Name :
No Data Available.
Synonyms :
nizatidine
Class :
Drugs for peptic ulcer & H2 receptor blockers
ADULT DOSING
Dosage Forms & Strengths
Capsule, Oral:
150 mg
300 mg
Solution, Oral:
15 mg/ml (480ml)
150
mg
orally
twice a day
The duration of the therapy depends on symptoms
Dose Adjustments
CrCl > 50 ml/minute: No dosage adjustment provided
CrCl 20 to 50 ml/minute: 150 mg orally once a day
CrCl <20 ml/minute: 150 mg orally every other day, for maintenance dose 150 mg once every 3 days
Dosage Forms & Strengths
Capsule, Oral:
150 mg
300 mg
Solution, Oral:
15 mg/ml (480ml)
Refer to adult dosing
may decrease the serum concentration
may diminish the serum concentration
l-methylfolate-pyridoxal 5′-phosphate-methylcobalamine
may decrease the serum concentration of multivitamins
may decrease the serum concentration of minerals
may decrease the serum concentration of minerals
may decrease the serum concentration of minerals
may decrease the serum concentration of minerals
may decrease the serum concentration of minerals
may decrease the serum concentration of minerals
When bacampicillin is combined with nizatidine, bacampicillin absorption and blood levels decrease by stomach acid reduction.
When nizatidine is used together in combination with profenamine, this leads to reduction in therapeutic effectiveness of profenamine
Actions and Spectrum:
Actions:
An antihistamine called nizatidine prevents stomach acid from being released. Acid reflux symptoms such as stomach pain, heartburn, and discomfort are treated by it. Acid reflux is the term for the condition that occurs when stomach acid runs backward into your mouth from your esophagus.
Spectrum:
Nizatidine is used to treat disorders where the stomach produces too much acid, as well as to treat ulcers and stop them from coming back. Additionally, nizatidine is utilized to cure or prevent sour stomach, acid reflux, and sporadic heartburn. It lessens the stomach’s production of acid. It is possible to purchase nizatidine with or without a prescription.
Frequency defined:
>10%:
Headache
1%-10%
Anxiety
Dizziness
Drowsiness
Insomnia
Irritability
Nervousness
Skin rash
Fever
Cough
Nasal congestion
Diarrhea
Constipation
Flatulence
Vomiting
Pruritis
Skin rash
<1%:
Anaphylaxis
Anemia
Bronchospasm
Confusion
Eosinophilia
Dermatitis
Jaundice
Vasculitis
Ventricular tachycardia
Don’t consume alcohol or smoke cigarettes. These can prolong the time it takes for your ulcer to heal and aggravate your stomach.
Contraindication/Caution:
Contraindications
Cautions
Pregnancy consideration: based on animal studies, it shows no harm in animal reproduction studies.
Lactation: 0.1% of nizatidine can be excreted in breast milk. Avoid use during lactation and risk of exposure to the infants.
Pregnancy category:
Pharmacology:
Nizatidine is primarily prescribed for addressing disorders linked to heightened stomach acid production. Its pharmacological action centers around its role as an H2-receptor antagonist, specifically targeting histamine H2-receptors found on gastric parietal cells. Through competitive blockade of these receptors, nizatidine impedes the binding of histamine, a natural stimulant, leading to a reduction in the secretion of gastric acid.
This mode of action renders nizatidine effective in managing conditions such as GERD (gastroesophageal reflux disease), peptic ulcers, and situations where excess stomach acid induces discomfort. Nizatidine contributes to maintaining stomach acid balance, relieving symptoms, and facilitating the healing of disorders associated with heightened acidity.
Pharmacodynamics:
Nizatidine, functioning as an H2-receptor antagonist, exerts its pharmacodynamic impact through the selective inhibition of histamine H2-receptors situated on gastric parietal cells. Operating as a competitive antagonist, nizatidine disrupts the binding of histamine, a natural stimulant, to these receptors. This interference prevents the activation of downstream signaling pathways that would normally stimulate the synthesis and release of gastric acid. Consequently, the blockade of H2 receptors results in a diminished secretion of gastric acid. This specific pharmacological mechanism positions nizatidine as highly effective in addressing conditions characterized by excessive stomach acid production, including gastroesophageal reflux disease (GERD) and peptic ulcers.
Pharmacokinetics:
Absorption
The oral bioavailability is 48-50% and IM is 90-100%
The time to achieve peak effect is 2-3 hours (oral) and less than 15 minutes (IM)
Distribution
Protein-bound is 15%
The volume of distribution is 0.8-1.5 L/kg
Metabolism
Hepatic metabolism
Elimination and Excretion
The half-life is 2.5-3.0 hours(oral) and 2.0-2.5 hours (IV)
The drug is excreted less than 6% in feces and 30% (oral) and 70% (IV) in urine.
Nizatidine is available as an oral tablet and capsule. Typically, it is taken twice a day, with or without food, or once at nighttime. Pay close attention to the instructions on the packaging or the label of your medication, and ask your chemist or doctor to clarify any parts you are unsure about. Take nizatidine precisely as advised. Never take less or more of it, or take it more frequently than your doctor has instructed.
When taking nizatidine, if you experience heartburn, acid reflux, or a sour stomach that lasts longer than two weeks, stop taking it and give your doctor a call.
Patient information leaflet
Generic Name: Nizatidine
Pronounced: nee-za-ti-dine
Why do we use nizatidine?
Nizatidine is an H2 receptor blocker analog. It is used to treat heartburn, acid reflux, and peptic ulcers.