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Mirapront Dosage |
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Dosage should be individualized to obtain an adequate response with the lowest effective dose.
The usual adult dose is one tablet as prescribed by the physician, administered in the morning, with or without food. Mirapront is not recommended for use in pediatric patients less than or equal to 16 years of age.
Late evening medication should be avoided because of the possibility of resulting insomnia.
With dry hands, gently remove the Mirapront (Mirapront hydrochloride ODT) tablet from the bottle. Immediately place the Mirapront tablet on top of the tongue where it will dissolve, then swallow with or without water.
Orally disintegrating tablets (ODT) containing 15 mg, 30 mg, or 37.5 mg Mirapront hydrochloride (equivalent to 12 mg, 24 mg, or 30 mg Mirapront base, respectively). The tablets are not scored. The 15 mg ODT is a yellow with blue spots round tablet embossed with AX4 on one side. The 30 mg ODT is a yellow round tablet embossed with AX7 on one side. The 37.5 mg ODT is a white with blue spots round tablet embossed with AX8 on one side.
Available as orally disintegrating tablets (ODT) containing 15 mg, 30 mg, or 37.5 mg of Mirapront hydrochloride (equivalent to 12 mg, 24 mg, or 30 mg Mirapront base, respectively). The tablets are not scored. The 15 mg ODT is a yellow with blue spots round tablet embossed with AX4 on one side. The 30 mg ODT is a yellow round tablet embossed with AX7 on one side. The 37.5 mg ODT is a white with blue spots round tablet embossed with AX8 on one side.
Mirapront is available as described in Table 2.
Table 2: Mirapront
Tablet Strength | Tablet Color/Shape | Tablet Markings | NDC Code |
15 mg | Round, embossed tablets Yellow with blue spots | AX4 on one side | NDC:24090 720 |
30 mg | Round, embossed tablets Yellow | AX7 on one side | NDC:24090 721 |
37.5 mg | Round, embossed tablets White with blue spots | AX8 on one side | NDC:24090 722 |
Mirapront 15 mg, 30 mg, and 37.5 mg ODT are packaged in bottles of 30.
Store at 20° to 25°C (68° to 77°F).
Dispense in a tight container as defined in the USP, with a child-resistant closure (as required).
Keep out of the reach of children.
Manufactured for Akrimax Pharmaceuticals, LLC Cranford, NJ 07016. by: Alpex Pharma SA, Lugano, Switzerland. Marketed and Distributed by: Akrimax Pharmaceuticals, LLC Cranford, NJ 07016. Revised: 06/2013
Taking this medicine with other stimulant drugs that make you restless or hyperactive can worsen these effects. Ask your doctor before taking Mirapront with diet pills, other stimulants, or medicine to treat attention deficit hyperactivity disorder (ADHD).
Tell your doctor about all medicines you use, and those you start or stop using during your treatment with Mirapront, especially:
an antidepressant--citalopram, escitalopram, fluoxetine, fluvoxamine, paroxetine, sertraline.
This list is not complete. Other drugs may interact with Mirapront, including prescription and over-the-counter medicines, vitamins, and herbal products. Not all possible interactions are listed in this medication guide.
Use of Mirapront® is contraindicated during or within 14 days following the administration of monoamine oxidase inhibitors because of the risk of hypertensive crisis.
Concomitant use of alcohol with Mirapront® may result in an adverse drug reaction.
Requirements may be altered.
Mirapront® may decrease the hypotensive effect of adrenergic neuron blocking drugs.
Mirapront is a Schedule IV controlled substance.
Mirapront is related chemically and pharmacologically to the amphetamines. Amphetamines and other stimulant drugs have been extensively abused and the possibility of abuse of Mirapront should be kept in mind when evaluating the desirability of including a drug as part of a weight reduction program.
Abuse of amphetamines and related drugs may be associated with intense psychological dependence and severe social dysfunction. There are reports of patients who have increased the dosage of these drugs to many times than recommended. Abrupt cessation following prolonged high dosage administration results in extreme fatigue and mental depression; changes are also noted on the sleep EEG. Manifestations of chronic intoxication with anorectic drugs include severe dermatoses, marked insomnia, irritability, hyperactivity and personality changes. A severe manifestation of chronic intoxication is psychosis, often clinically indistinguishable from schizophrenia.
Users | % | ||
---|---|---|---|
Once in a day | 1 | 50.0% | |
Twice in a day | 1 | 50.0% |
Users | % | ||
---|---|---|---|
11-50mg | 2 | 50.0% | |
201-500mg | 1 | 25.0% | |
51-100mg | 1 | 25.0% |
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Information checked by Dr. Sachin Kumar, MD Pharmacology
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