BUSPIRONE HYDROCHLORIDE tablet

Negara: Amerika Serikat

Bahasa: Inggris

Sumber: NLM (National Library of Medicine)

Bahan aktif:

BUSPIRONE HYDROCHLORIDE (UNII: 207LT9J9OC) (BUSPIRONE - UNII:TK65WKS8HL)

Tersedia dari:

REMEDYREPACK INC.

INN (Nama Internasional):

BUSPIRONE HYDROCHLORIDE

Komposisi:

BUSPIRONE HYDROCHLORIDE 15 mg

Rute administrasi :

ORAL

Jenis Resep:

PRESCRIPTION DRUG

Indikasi Terapi:

Buspirone hydrochloride tablets are indicated for the management of anxiety disorders or the short-term relief of the symptoms of anxiety. Anxiety or tension associated with the stress of everyday life usually does not require treatment with an anxiolytic. The efficacy of buspirone hydrochloride tablets have been demonstrated in controlled clinical trials of outpatients whose diagnosis roughly corresponds to Generalized Anxiety Disorder (GAD). Many of the patients enrolled in these studies also had coexisting depressive symptoms and buspirone hydrochloride tablets relieved anxiety in the presence of these coexisting depressive symptoms. The patients evaluated in these studies had experienced symptoms for periods of 1 month to over 1 year prior to the study, with an average symptom duration of 6 months. Generalized Anxiety Disorder (300.02) is described in the American Psychiatric Association’s Diagnostic and Statistical Manual, III 1 as follows: Generalized, persistent anxiety (of at least 1 month continual duration), manifested by symptoms from three of the four following categories: 1.      Motor tension: Shakiness, jitteriness, jumpiness, trembling, tension, muscle aches, fatigability, inability to relax, eyelid twitch, furrowed brow, strained face, fidgeting, restlessness, easy startle. 2.      Autonomic hyperactivity: Sweating, heart pounding or racing, cold, clammy hands, dry mouth, dizziness, lightheadedness, paresthesias (tingling in hands or feet), upset stomach, hot or cold spells, frequent urination, diarrhea, discomfort in the pit of the stomach, lump in the throat, flushing, pallor, high resting pulse and respiration rate. 3.      Apprehensive expectation: Anxiety, worry, fear, rumination, and anticipation of misfortune to self or others. 4.      Vigilance and scanning: Hyperattentiveness resulting in distractibility, difficulty in concentrating, insomnia, feeling "on edge," irritability, impatience. The above symptoms would not be due to another mental disorder, such as a depressive disorder or schizophrenia. However, mild depressive symptoms are common in GAD. The effectiveness of buspirone hydrochloride tablets in long-term use, that is, for more than 3 to 4 weeks, has not been demonstrated in controlled trials. There is no body of evidence available that systematically addresses the appropriate duration of treatment for GAD. However, in a study of long-term use, 264 patients were treated with buspirone hydrochloride tablets for 1 year without ill effect. Therefore, the physician who elects to use buspirone hydrochloride tablets for extended periods should periodically reassess the usefulness of the drug for the individual patient. Buspirone hydrochloride tablets are contraindicated in patients hypersensitive to buspirone hydrochloride. The use of monoamine oxidase inhibitors (MAOIs) intended to treat depression with buspirone or within 14 days of stopping treatment with buspirone is contraindicated because of an increased risk of serotonin syndrome and/or elevated blood pressure. The use of buspirone within 14 days of stopping an MAOI intended to treat depression is also contraindicated. Starting buspirone in a patient who is being treated with reversible MAOIs such as linezolid or intravenous methylene blue is also contraindicated because of an increased risk of serotonin syndrome. (see WARNINGS , DOSAGE AND ADMINISTRATION  and DRUG INTERACTIONS ) Controlled Substance Class: Buspirone hydrochloride is not a controlled substance. Physical and Psychological Dependence: In human and animal studies, buspirone has shown no potential for abuse or diversion and there is no evidence that it causes tolerance, or either physical or psychological dependence. Human volunteers with a history of recreational drug or alcohol usage were studied in two double-blind clinical investigations. None of the subjects were able to distinguish between buspirone hydrochloride tablets and placebo. By contrast, subjects showed a statistically significant preference for methaqualone and diazepam. Studies in monkeys, mice, and rats have indicated that buspirone lacks potential for abuse. Following chronic administration in the rat, abrupt withdrawal of buspirone did not result in the loss of body weight commonly observed with substances that cause physical dependency. Although there is no direct evidence that buspirone hydrochloride tablets causes physical dependence or drug-seeking behavior, it is difficult to predict from experiments the extent to which a CNS-active drug will be misused, diverted, and/or abused once marketed. Consequently, physicians should carefully evaluate patients for a history of drug abuse and follow such patients closely, observing them for signs of buspirone hydrochloride tablets misuse or abuse (e.g., development of tolerance, incrementation of dose, drug-seeking behavior).

Ringkasan produk:

Buspirone Hydrochloride Tablets USP, 15 mg are white to off-white, capsule-shaped, flat-faced, beveled-edge tablets, bisected on one side and trisected on other side. The trisected side of tablet is debossed with '5' on each trisect segment. The bisected side is debossed with 'ZE', on one bisect and '38' on other bisect segment and are supplied as follows: NDC: 70518-1050-00 NDC: 70518-1050-01 PACKAGING: 30 in 1 BLISTER PACK PACKAGING: 60 in 1 BLISTER PACK Storage: Store at 20°C to 25° C (68°F to 77° F) [See USP Controlled Room Temperature]. Dispense in a tight, light-resistant container. Repackaged and Distributed By: Remedy Repack, Inc. 625 Kolter Dr. Suite #4 Indiana, PA 1-724-465-8762

Status otorisasi:

Abbreviated New Drug Application

Selebaran informasi

REMEDYREPACK INC.
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Patient Instruction Sheet
Buspirone Hydrochloride Tablets, USP
HOW TO USE
For 15 mg and 30 mg tablets
Response to buspirone varies among individuals. Your physician may
find it necessary to
adjust your dosage to obtain the proper response.
Each tablet is scored and can be broken accurately to provide any of
the following dosages.
To break a tablet accurately and easily, hold the tablet between your
thumbs and index fingers close to the
appropriate tablet score (groove) as shown in the photo. Then, with
the tablet score facing you, apply
pressure and snap the tablet segments apart (segments breaking
incorrectly should not be used).
Call your doctor for medical advice about side effects. You may report
side effects to FDA at 1-800-
FDA-1088.
Repackaged By / Distributed By: RemedyRepack Inc.
625 Kolter Drive, Indiana, PA 15701
[phone]
Revised: 2/2024
Document Id: 115bb722-e67c-fef3-e063-6294a90a6d8f
34391-3
Set id: 40aa4d7c-0342-4614-b745-7396e7a56ca8
Version: 10
Effective Time: 20240214
REMEDYREPACK INC.

Karakteristik produk

BUSPIRONE HYDROCHLORIDE- BUSPIRONE HYDROCHLORIDE TABLET
REMEDYREPACK INC.
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BUSPIRONE HYDROCHLORIDE TABLETS, USP
DESCRIPTION
Buspirone hydrochloride tablets, USP are an antianxiety agent that is
not chemically or
pharmacologically related to the benzodiazepines, barbiturates, or
other
sedative/anxiolytic drugs.
Buspirone hydrochloride, USP is a white crystalline powder. It is very
soluble in water;
freely soluble in methanol and in methylene chloride; sparingly
soluble in ethanol and in
acetonitrile; very slightly soluble in ethyl acetate and practically
insoluble in hexanes. Its
molecular weight is 422. Chemically, buspirone hydrochloride is
8-[4-[4-(2-pyrimidinyl)-
1-piperazinyl]butyl]-8-azaspiro[4.5]decane-7,9-dione
monohydrochloride. The molecular
formula C21H31N5O2•HCl is represented by the following structural
formula:
Each buspirone hydrochloride tablet intended for oral administration
contains 5 mg or
7.5 mg or 10 mg or 15 mg or 30 mg buspirone hydrochloride (equivalent
to 4.6 mg,
6.85 mg, 9.1 mg, 13.7 mg, and 27.4 mg of buspirone free base,
respectively). In
addition, each tablet contains the following inactive ingredients:
colloidal silicon dioxide,
lactose monohydrate, magnesium stearate, microcrystalline cellulose
and sodium starch
glycolate. The 5 mg and 10 mg tablets are scored so they can be
bisected. Thus, the 5
mg tablet can also provide 2.5 mg dose, and the 10 mg tablet can
provide a 5 mg dose.
The 15 mg and 30 mg tablets are scored so they can be either bisected
or trisected.
Thus, a single 15 mg tablet can provide the following doses: 15 mg
(entire tablet), 10 mg
(two thirds of a tablet), 7.5 mg (one half of a tablet), or 5 mg (one
third of a tablet). A
single 30 mg tablet can provide the following doses: 30 mg (entire
tablet), 20 mg (two
thirds of a tablet), 15 mg (one half of a tablet), or 10 mg (one third
of a tablet).
CLINICAL PHARMACOLOGY
The mechanism of action of buspirone is unknown. Buspirone differs
from typical
benzodiazepine anxiolytics in that it does not exert anticonv