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FEVARIN™ 100mg 30 Tablets Buy Online
Understanding FEVARIN Tablets 100mg
FEVARIN 100mg tablets are a medication used to treat specific mental health conditions. Understanding its role and proper usage is crucial for effective management. This overview provides essential information about this important treatment option. Always consult your physician before starting or altering any medication regimen.
The active ingredient in FEVARIN is fluvoxamine, a selective serotonin reuptake inhibitor (SSRI). SSRIs work by increasing the levels of serotonin, a neurotransmitter vital for mood regulation, in the brain. This mechanism helps alleviate symptoms associated with various mental health disorders.
FEVARIN is primarily prescribed for depression and obsessive-compulsive disorder (OCD). It is also sometimes used to treat other conditions, but this should always be determined by a qualified healthcare professional based on individual needs and circumstances. The effectiveness of FEVARIN varies from person to person.
A Comprehensive Overview
FEVARIN 100mg tablets, containing the active ingredient fluvoxamine, are categorized as a selective serotonin reuptake inhibitor (SSRI). This class of antidepressants works by increasing the availability of serotonin, a neurotransmitter crucial for regulating mood, sleep, and other cognitive functions. Fluvoxamine’s impact on serotonin levels is believed to be the primary mechanism by which it alleviates symptoms of depression and obsessive-compulsive disorder (OCD).
The medication is available in a film-coated tablet form, designed for oral administration. Dosage and frequency are determined by a healthcare professional based on individual patient needs and response to treatment. It’s vital to adhere precisely to the prescribed regimen, as adjustments should only be made under medical supervision. Improper use could lead to reduced efficacy or adverse effects.
Before initiating FEVARIN treatment, a thorough medical evaluation is essential. Patients with a history of certain medical conditions, such as seizures or liver impairment, may require additional monitoring or alternative treatment options. Open communication with your doctor concerning any existing health issues or medications is paramount to ensure safe and effective use. Regular check-ups allow for adjustments to the treatment plan as needed.
The effects of FEVARIN are not immediate; it often takes several weeks before noticeable improvements in symptoms are observed. Patients should be patient and consistent in their adherence to the prescribed treatment plan. While FEVARIN is generally well-tolerated, potential side effects should be discussed with your physician. Early identification and management of any adverse effects can help optimize treatment outcomes.
Mechanism of Action
FEVARIN’s primary mechanism involves the selective inhibition of serotonin reuptake. Serotonin, a crucial neurotransmitter, plays a vital role in regulating mood, sleep, and various cognitive functions. By blocking the reabsorption of serotonin, fluvoxamine increases its concentration in the synaptic cleft, enhancing serotonergic neurotransmission.
This increased serotonin availability at receptor sites throughout the brain is believed to be the primary reason for FEVARIN’s efficacy in treating depression and OCD. The precise pathways and interactions involved are complex and not fully understood, but the enhancement of serotonergic activity is central to its therapeutic effect. Further research continues to explore the nuances of fluvoxamine’s action.
While primarily a serotonin reuptake inhibitor, fluvoxamine also exhibits some affinity for sigma-1 receptors. The significance of this interaction in its overall therapeutic effect is still under investigation; however, it may contribute to its clinical benefits in specific patient populations or in certain symptom domains. The interaction with these receptors adds another layer of complexity to its mechanism.
Importantly, fluvoxamine demonstrates minimal affinity for other neurotransmitter receptors, such as alpha- and beta-adrenergic, histaminergic, muscarinic, or dopaminergic receptors. This selective action contributes to a generally better side effect profile compared to some older antidepressants that interact with a broader range of receptors. This selectivity is a key feature distinguishing fluvoxamine within the SSRI class.
Dosage and Administration
FEVARIN 100mg tablets are for oral administration only. They should be swallowed whole with water; do not crush or chew the tablets. Dosage is determined by a healthcare professional and is highly individualized, depending on the specific condition being treated and the patient’s response to therapy. Always follow your physician’s instructions precisely.
For adults with depression, a typical starting dose might be 50mg daily, often increasing gradually over several days to a target dosage of 100-300mg per day. Higher daily dosages (above 150mg) are usually divided into two or three separate administrations to optimize tolerability. The specific dosing schedule and duration of treatment are dependent on clinical response and should be tailored to the individual.
In the treatment of obsessive-compulsive disorder (OCD), a similar approach is often employed, beginning with a lower dose and gradually increasing as tolerated. The effective daily dose for OCD typically ranges from 100mg to 300mg. Again, the dosage should be carefully managed by the prescribing physician based on the patient’s response and overall health status. Regular monitoring is essential to assess efficacy and safety.
It is crucial to understand that FEVARIN treatment requires careful titration of dosage. Rapid changes in dosage are generally not recommended. Adjustments should be made gradually, under the guidance of a healthcare provider, to minimize the risk of adverse events and optimize treatment outcomes. Close monitoring for side effects is also crucial during dosage adjustments.
Therapeutic Uses
FEVARIN 100mg tablets are primarily indicated for the treatment of two significant mental health conditions: major depressive disorder (MDD) and obsessive-compulsive disorder (OCD). These conditions share some overlapping symptoms but are distinct disorders requiring tailored therapeutic approaches. FEVARIN’s effectiveness stems from its ability to modulate serotonin levels in the brain.
In major depressive disorder, FEVARIN helps alleviate core symptoms such as persistent sadness, loss of interest or pleasure, feelings of hopelessness, and significant changes in sleep or appetite. By increasing serotonin availability, it aims to improve mood, motivation, and overall functioning. The duration of treatment for depression typically extends beyond the initial resolution of symptoms to prevent relapse.
For obsessive-compulsive disorder, FEVARIN targets the distressing obsessions (recurring intrusive thoughts) and compulsions (repetitive behaviors) that characterize this condition. By reducing the anxiety associated with obsessions and the need to engage in compulsions, FEVARIN aims to improve quality of life and reduce the significant impairment that OCD can cause. Treatment often requires long-term management to maintain improvement.
While primarily used for MDD and OCD, FEVARIN may occasionally be considered for other conditions under specific circumstances and with careful evaluation by a healthcare professional. These off-label uses should always be guided by clinical expertise and a thorough assessment of potential benefits and risks. Always discuss all treatment options with your doctor to determine the most appropriate course of action for your individual needs.
Pharmacokinetics
Understanding the pharmacokinetic profile of FEVARIN, specifically how the body processes fluvoxamine, is crucial for optimizing treatment. Fluvoxamine’s pharmacokinetics encompass its absorption, distribution, metabolism, and excretion. These processes influence the drug’s concentration in the bloodstream and its overall therapeutic effect.
Following oral administration, fluvoxamine is extensively absorbed from the gastrointestinal tract. Peak plasma concentrations are typically observed within a timeframe of approximately 3-8 hours. Food does not significantly affect its absorption, making it convenient for patients. However, individual variations in absorption can occur.
Fluvoxamine is extensively metabolized primarily in the liver, primarily through oxidative demethylation involving the cytochrome P450 enzyme system. This metabolism generates several metabolites, some of which possess minimal pharmacological activity. The drug’s elimination half-life, typically ranging from 13 to 15 hours after a single dose, can be slightly prolonged with repeated administration.
Elimination of fluvoxamine and its metabolites occurs primarily through renal excretion. Patients with hepatic or renal impairment may experience altered pharmacokinetics, potentially requiring dosage adjustments or alternative treatment strategies. Careful monitoring is essential in these patient populations to ensure therapeutic efficacy and safety while minimizing the risk of adverse effects.
Absorption and Distribution
Following oral ingestion, fluvoxamine, the active component of FEVARIN, undergoes a process of absorption into the bloodstream primarily via the gastrointestinal tract. This absorption is generally considered to be complete, although the rate can vary between individuals. The presence of food does not significantly impact absorption, making administration convenient for patients.
Once absorbed, fluvoxamine distributes throughout the body, reaching various tissues and organs. A significant proportion of fluvoxamine binds to plasma proteins, influencing its distribution and availability at target sites within the central nervous system. The volume of distribution is relatively large, suggesting that fluvoxamine distributes extensively into body tissues beyond the bloodstream.
The extent to which fluvoxamine penetrates the blood-brain barrier, allowing it to reach its sites of action in the brain, is a critical factor in its therapeutic efficacy. The drug’s ability to cross this barrier effectively contributes to its ability to modulate neurotransmitter function and alleviate symptoms of depression and OCD. Further research continues to refine our understanding of these processes.
Individual variations in absorption and distribution can be influenced by factors such as age, liver and kidney function, and concurrent medications. These factors can impact the drug’s overall effectiveness and the potential for side effects. Healthcare providers must consider these factors when determining appropriate dosages and monitoring patient responses.
Elimination
The elimination of fluvoxamine from the body is a multi-stage process involving both metabolism and excretion. The primary route of elimination is through the kidneys, with fluvoxamine and its metabolites being excreted in the urine. A smaller portion may also be eliminated through fecal excretion. Understanding these pathways is crucial for managing potential drug interactions and adjusting dosages in patients with impaired renal function.
Hepatic metabolism plays a significant role in the elimination process. Fluvoxamine undergoes extensive metabolism in the liver, primarily via the cytochrome P450 enzyme system, leading to the formation of various metabolites. Some of these metabolites retain minimal pharmacological activity, while others are largely inactive. The efficiency of this metabolic process can vary between individuals, influenced by factors like genetics and liver health.
The elimination half-life of fluvoxamine, representing the time it takes for the drug’s concentration in the blood to decrease by half, is typically in the range of 13 to 15 hours after a single dose. This half-life can be slightly extended with repeated dosing, leading to a steady-state concentration over several days. This half-life determines the frequency of dosing required to maintain therapeutic levels.
In patients with hepatic or renal impairment, the elimination of fluvoxamine may be significantly altered. Reduced hepatic function can lead to slower metabolism, while impaired renal function can result in decreased excretion. Consequently, dosage adjustments are often necessary in such patients to prevent drug accumulation and the risk of adverse effects. Careful monitoring of serum levels and clinical response is crucial in these situations.
Potential Side Effects
While generally well-tolerated, FEVARIN, like other medications, can cause side effects. The incidence and severity of these side effects vary widely among individuals. Some side effects are common and usually mild, while others are less frequent but may require medical attention. It’s crucial to report any concerning symptoms to your healthcare provider.
Common side effects often include gastrointestinal disturbances such as nausea, vomiting, and diarrhea. These effects are usually mild and tend to subside as the body adjusts to the medication. Other frequently reported side effects include drowsiness, dizziness, and headaches. These can impact daily activities and should be discussed with your doctor.
Less common but more serious side effects may include changes in heart rate (tachycardia or bradycardia), decreased blood pressure (hypotension), and liver function abnormalities. Rarely, serious allergic reactions can occur. Patients should be vigilant for any signs of allergic reaction, such as skin rash, hives, or difficulty breathing, and seek immediate medical help if they arise.
The risk of certain side effects, such as serotonin syndrome (a rare but potentially life-threatening condition), is increased when FEVARIN is taken in conjunction with other serotonergic medications. It is imperative to inform your healthcare provider of all medications, including over-the-counter drugs and herbal supplements, you are currently taking or plan to take to minimize the risk of drug interactions and adverse effects. Open communication with your doctor is vital for safe medication use.
Cons
Precautions and Contraindications
Before starting FEVARIN, it’s crucial to inform your doctor about your complete medical history, including any pre-existing conditions. Certain conditions may necessitate caution or contraindicate the use of FEVARIN altogether. Open communication with your physician is key to ensuring safe and effective treatment.
Patients with a history of seizures or epilepsy should exercise particular caution. Fluvoxamine can potentially lower the seizure threshold, increasing the risk of seizures in susceptible individuals. Close monitoring is necessary, and alternative treatments may be considered in some cases. Regular neurological assessments may be required.
Individuals with liver or kidney impairment should be carefully monitored during FEVARIN therapy. These organs play a crucial role in the metabolism and excretion of the drug. Impaired function can lead to drug accumulation, increasing the risk of side effects. Dosage adjustments or alternative treatments may be necessary.
Pregnancy and breastfeeding warrant special consideration. While the use of FEVARIN during pregnancy is generally avoided unless the benefits clearly outweigh the risks, the decision should be made in close consultation with a healthcare professional. Fluvoxamine can pass into breast milk, potentially affecting the nursing infant. Alternative treatment options should be considered for breastfeeding mothers.
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