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Niacinamide
Pronunciation
Generic Available
Synonyms
Pharmacological Index
Use
Pregnancy Risk Factor
Contraindications
Warnings/Precautions
Adverse Reactions
Overdosage/Toxicology
Drug Interactions
Mechanism of Action
Pharmacodynamics/Kinetics
Usual Dosage
Test Interactions
Mental Health: Effects on Mental Status
Mental Health: Effects on Psychiatric Treatment
Dental Health: Local Anesthetic/Vasoconstrictor Precautions
Dental Health: Effects on Dental Treatment
Dosage Forms
References

Pronunciation
(nye a SIN a mide)

Generic Available

Yes


Synonyms
Nicotinamide; Vitamin B3

Pharmacological Index

Vitamin, Water Soluble


Use

Prophylaxis and treatment of pellagra


Pregnancy Risk Factor

A (C if used in doses greater than RDA suggested doses)


Contraindications

Hypersensitivity to niacin or niacinamide; liver disease; active peptic ulcer; severe hypotension; arterial hemorrhage


Warnings/Precautions

Use caution in heavy ethanol users, unstable angina or CAD (risk of arrhythmias at high doses), diabetes (interfere with glucose control), renal disease, active gallbladder disease (can exacerbate), gout, or allergies. Avoid large pharmacological amounts in patients with a history of liver disease. Monitor liver function tests with high doses.


Adverse Reactions

Percentage unknown: Tachycardia, rash, bloating, flatulence, nausea, paresthesia in extremities, blurred vision, wheezing, increased sebaceous gland activity


Overdosage/Toxicology

Symptoms of overdose include GI distress

Treatment is supportive


Drug Interactions

Oral hypoglycemics: Effect may be decreased by niacin.

Sulfinpyrazone and probenecid; niacin may inhibit uricosuric effects.

Aspirin decreases adverse effect of flushing.

Lovastatin (and possibly other HMG CoA reductase inhibitors): Increased risk of toxicity (myopathy).

Adrenergic blocking agents additive vasodilating effect and postural hypotension.


Mechanism of Action

Used by the body as a source of niacin; is a component of two coenzymes which is necessary for tissue respiration, lipid metabolism, and glycogenolysis; inhibits the synthesis of very low density lipoproteins; does not have hypolipidemia or vasodilating effects


Pharmacodynamics/Kinetics

Absorption: Rapid from GI tract

Metabolism: In the liver

Half-life: 45 minutes

Time to peak serum concentration: 20-70 minutes

Elimination: In urine


Usual Dosage

Oral:

Adults: 50 mg 3-10 times/day

Pellagra: 300-500 mg/day

Recommended daily allowance: 13-19 mg/day


Test Interactions

False elevations of urinary catecholamines in some fluorometric determinations


Mental Health: Effects on Mental Status

None noted


Mental Health: Effects on Psychiatric Treatment

None noted


Dental Health: Local Anesthetic/Vasoconstrictor Precautions

No information available to require special precautions


Dental Health: Effects on Dental Treatment

No effects or complications reported


Dosage Forms

Tablet: 50 mg, 100 mg, 125 mg, 250 mg, 500 mg


References

Gugler R, "Clinical Pharmacokinetics of Hypolipidaemic Drugs," Clin Pharmacokinet, 1978, 3(6):425-39.

LeWitt PA, "The Neurotoxicity of the Rat Poison Vacor. A Clinical Study of 12 Cases," N Engl J Med, 1980, 302(2):73-7.

Ovesen L, "Vitamin Therapy in the Absence of Obvious Deficiency: What Is the Evidence?" Drugs, 1984, 27(2):148-70.


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