Advances in pharmacological and pharmaceutical sciences

Advances in pharmacological and pharmaceutical sciences suggest you

advances in pharmacological and pharmaceutical sciences are

Missed DoseIf you miss a dose, take it as soon as you remember. StorageStore at room temperature away from light and moisture. Information last revised May 2020. Copyright(c) 2020 First Databank, Inc. Top of the pageTopic ContentsUsesOther UsesHow To UseSide EffectsPrecautionsDrug InteractionsOverdoseNotesMissed DoseStorageThis information does not replace the advice of a doctor.

Paroxetine is a selective serotonin reuptake inhibitor (SSRI). Chlorzoxazone Tablets (Lorzone)- Multum is used to treat several diseases, including major depressive disorder, obsessive-compulsive disorder, social anxiety disorder, panic disorder, posttraumatic stress disorder, generalized anxiety disorder, and premenstrual dysphoric disorder.

It is used in the treatment of hot flashes and night sweats that are associated with menopause. This activity outlines the indications, mechanism advances in pharmacological and pharmaceutical sciences action, methods of administration, advances in pharmacological and pharmaceutical sciences adverse effects, contraindications, monitoring, and toxicity of paroxetine, so providers can direct patient therapy in treating conditions for which it is indicated as part of the interprofessional team.

Objectives: Identify the mechanism of action of paroxetine. Outline the indications for initiating therapy with paroxetine. Review the adverse event profile for paroxetine. Review the importance of improving care coordination among the interprofessional team to enhance care delivery for patients who can benefit from therapy with paroxetine.

Paroxetine is a selective serotonin reuptake inhibitor (SSRI) and, as such, is identified as an antidepressant. It is FDA approved for major depressive disorder (MDD), obsessive-compulsive disorder (OCD), social anxiety disorder (SAD), panic disorder, posttraumatic stress disorder (PTSD), generalized anxiety disorder (GAD), and premenstrual dysphoric disorder (PMDD), vasomotor symptoms associated with menopause.

As an SSRI class drug, paroxetine's signature mechanism energy increase action is to block the serotonin reuptake transporter (SERT) and thus increase the concentration of synaptic serotonin.

Current theory suggests that the diminished serotonin concentration in the depressed brain induces the upregulation of serotonergic receptors. By increasing the synaptic serotonin concentration, paroxetine thus induces the downregulation of the previously upregulated serotonin receptors, thus normalizing the receptor concentration.

Paroxetine is administered orally. The medication should be titrated based on the patient's symptoms and tolerance to dosage. The drug can be taken with or without food. In addition to regular tablets, it is available in a controlled-release tablet and liquid form.

Paroxetine may be administered at any time of the day, depending on toleration. Paroxetine undergoes metabolism via hepatic CYPP450 2D6. Many of the side effects locator paroxetine are dose-dependent. The most common side effects include drowsiness, dry mouth, loss of appetite, sweating, sleep disturbance, and sexual side effects.

Clinicians can address sexual side effects medications like advances in pharmacological and pharmaceutical sciences. Withdrawal symptoms from discontinuation include haemorrhoids, lethargy, advances in pharmacological and pharmaceutical sciences, vomiting, headache, fever, chills, vivid dreams, electric shock-like-sensation, dyskinesia, anxiety, crying, irritability, and depersonalization.

Absolute contraindications include concurrent advances in pharmacological and pharmaceutical sciences ls models young monoamine oxidase inhibitors (MAOIs), thioridazine, and pimozide. Concomitant use of MAOIs and paroxetine can precipitate serotonin syndrome. Paroxetine inhibits TCA metabolism, leading to possible TCA toxicity.

Paroxetine is not recommended for use during pregnancy or if breastfeeding. Based on epidemiological studies, therapy exposed to paroxetine during the first trimester had an increased risk for cardiovascular malformations.

Labs should include serum sodium concentration to rule out SIADH. Serotonin syndrome precipitates via the manifestation of changes in mental status, autonomic instability, gastrointestinal symptoms, hyperreflexia, and myoclonus.

Serotonin syndrome is treated by discontinuing any of the offending agents. If symptoms continue to escalate, the clinician can administer cyproheptadine.

The treatment for overdose includes symptomatic supportive treatment. There is no specific treatment for paroxetine toxicity. This team starts with the prescribing clinicians (MD, DO, PA, NP), who will make the initial determination for using paroxetine.

Open communication between various disciplines, such as pharmacy and psychiatry, can benefit the patient. The pharmacist can provide the dosing for the patient and monitor toxicity levels and consult with the prescriber for changes. This advances in pharmacological and pharmaceutical sciences allows the patient to have a correct dosage based on their co-morbid conditions.

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