Ansiten tablets

Ansiten

  • Active Ingredient: Buspirone
  • 10 mg, 5 mg
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What is Ansiten?

The active ingredient of Ansiten brand is buspirone. Buspirone is an anti-anxiety medicine that affects chemicals in the brain that may be unbalanced in people with anxiety. Each tablet, for oral administration, contains 5 mg, 7.5 mg, 10 mg, 15 mg or 30 mg of Buspirone hydrochloride, USP (equivalent to 4.6 mg, 6.9 mg, 9.1 mg, 13.7 mg and 27.4 mg of Buspirone free base, respectively). The 5 mg and 10 mg tablets are scored so they can be bisected. Thus, the 5 mg tablet can also provide a 2.5 mg dose, and the 10 mg tablet can provide a 5 mg dose. The 15 mg tablets are scored such that they may be bisected or trisected. Thus, a single 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). The 30 mg tablets are scored such that they may be bisected or trisected. Thus, a single 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). Buspirone hydrochloride tablets, USP contain the following inactive ingredients: colloidal silicon dioxide, lactose monohydrate, magnesium stearate, microcrystalline cellulose, and sodium starch glycolate.

Used for

Ansiten is used to treat diseases such as: Anxiety, Borderline Personality Disorder, Panic Disorder, Sexual Dysfunction, SSRI Induced.

Side Effect

Possible side effects of Ansiten include: uncontrolled movements of the body; decreased concentration; stiffness of the arms or legs; ringing in the ears; muscle pain, spasms, cramps, or stiffness; clamminess or sweating; very small pupils of the eyes; dryness of the mouth.

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Inhibitors And Inducers Of Cytochrome P450 3A4 (CYP3A4)

Ansiten has been shown in vitro to be metabolized by CYP3A4. This finding is consistent with the in vivo interactions observed between Ansiten and the following:

Rated Ansiten (BuSpar) for Anxiety Report

I started taking this for severe anxiety and panic attacks. My dr put me on 15mg once a day. The first week was ok then I started having horrible panic attacks. Worse than I have ever experienced. Along with a horrible headache and diarrhea. I stopped taking it and with in 24 hours I am feeling so much better. I know it's a miracle drug for some but it made my life way worse.

Itraconazole

In a study in healthy volunteers, coadministration of Ansiten (10 mg as a single dose) with itraconazole (200 mg/day for 4 days) increased plasma Ansiten concentrations (13-fold increase in Cmax and 19-fold increase in AUC). These pharmacokinetic interactions were accompanied by an increased incidence of side effects attributable to Ansiten. If the two drugs are to be used in combination, a low dose of Ansiten (e.g., 2.5 mg q.d.) is recommended. Subsequent dose adjustment of either drug should be based on clinical assessment.

More common side effects

The more common side effects that can occur with use of Ansiten include:

  • dizziness
  • nausea
  • headache
  • nervousness
  • lightheadedness
  • excitement

If these effects are mild, they may go away within a few days or a couple of weeks. If they’re more severe or don’t go away, talk to your doctor or pharmacist.

What are Ansiten and Xanax?

Ansiten is used for the treatment of anxiety. Its mechanism of action is not clearly understood but may involve effects on the neurotransmitters serotonin and dopamine. Ansiten may work by stimulating serotonin type 1A receptors on nerves, thereby altering the chemical messages that nerves receive. Unlike medications for anxiety of the benzodiazepine class, Ansiten does not cause sedation.

Xanax (alprazolam) is an anti-anxiety medication in the benzodiazepine family, the same family that includes diazepam (Valium), clonazepam (Klonopin), lorazepam (Ativan), and flurazepam (Dalmane). Xanax and other benzodiazepines act by enhancing the effects of a neurotransmitter called gamma-aminobutyric acid (GABA) in the brain. GABA inhibits activity in the brain. It is believed that excessive activity in the brain may cause anxiety or other psychiatric disorders.

Rated Ansiten (BuSpar) for Anxiety Report

I’ve been taking Ansiten for about 2 weeks And Kalonopin for about a month now and everytime I take it almost immediately after I feel incredibly dizzy and I get these weird rushes through my body like vertigo almost. The Clonopin helped with my anxiety significantly and I experienced no side effects. Obviously my Health care physician did not want me to be on this long term and only wanted me to take it on an as needed basis from now on. However, ever since I started using BuSpar my mood has become strange and I don’t feel like myself. Recently i’ve experienced terrible panic attacks and my anxiety is now worse than ever. I’m frustrated because I’ve tried so many medications and none of them have worked accept for benzos.

Rated Ansiten (BuSpar) for Anxiety Report

This drug caused severe headaches and asthma-like breathing problems which was really frightening.

WARNINGS

The administration of Ansiten hydrochloride tablets to a patient taking a monoamine oxidase inhibitor (MAOI) may pose a hazard. There have been reports of the occurrence of elevated blood pressure when Ansiten hydrochloride tablets have been added to a regimen including an MAOI. Therefore, it is recommended that Ansiten hydrochloride tablets not be used concomitantly with an MAOI.

Because Ansiten hydrochloride tablets have no established antipsychotic activity, it should not be employed in lieu of appropriate antipsychotic treatment.

Ansiten

An anti-anxiolytic psychotropic agent of the azaspirodecanedione class, which is unrelated to benzodiazepines, barbiturates or other sedatives.

Adverse effectsDizziness, insomnia, nervousness, drowsiness, lightheadedness, nausea, diarrhoea, headache, fatigue.

WarningAvoid MAOIs when using Ansiten.

RouteOral and transdermal; initial adult dosage is 15 mg/day; maximum, 60 mg/day.

Mechanism of actionAnsiten has an affinity for both serotonin (5-HT1A) and dopamine (D2) receptors; its mechanism of action is currently unknown.


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