Atogard 60 mg (Atomoxetine)
64.00$ – 163.50$Price range: 64.00$ through 163.50$
Product Overview Atogard 60 mg is a prescription medication that contains the active ingredient Atomoxetine. It is manufactured by Fortune Healthcare Pvt. Ltd. and is specifically indicated for the treatment of Attention Deficit Hyperactivity Disorde
| Pack Size | Price | Quantity | |
|---|---|---|---|
| 50 Tablet/s | 64.00$ | ||
| 100 Tablet/s | 102.20$ | ||
| 200 Tablet/s | 163.50$ |
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Product Overview
Atogard 60 mg is a prescription medication that contains the active ingredient Atomoxetine. It is manufactured by Fortune Healthcare Pvt. Ltd. and is specifically indicated for the treatment of Attention Deficit Hyperactivity Disorder (ADHD) in children, adolescents, and adults.
What is Atogard 60 mg (Atomoxetine)
Atomoxetine belongs to a class of medicines known as selective norepinephrine reuptake inhibitors (NRI). Unlike stimulant ADHD drugs, Atogard works by increasing the amount of norepinephrine available in the brain, which helps improve focus, impulse control, and attention.
Fortune Healthcare produces Atogard in tablet form, each strip containing ten 60 mg tablets. The medication is marketed for patients who require a non‑stimulant option for managing ADHD symptoms.
Uses and Benefits
The primary use of Atogard 60 mg is to reduce the core symptoms of ADHD, including inattention, hyperactivity, and impulsivity. Clinical studies have shown that Atomoxetine can improve academic performance, reduce classroom disruptions, and enhance overall quality of life for individuals with ADHD.
Additional benefits may include:
- Improved concentration and task completion
- Reduced impulsive behavior
- Better emotional regulation
- Long‑term symptom control without the need for daily dosing of stimulants
Because it is not a controlled substance, Atogard can be an appropriate choice for patients with a history of substance misuse or for those who experience intolerable side effects from stimulant medications.
How It Works
Atogard functions by selectively inhibiting the reuptake of norepinephrine, a neurotransmitter involved in attention and alertness. By blocking the norepinephrine transporter, the drug increases the concentration of norepinephrine in the prefrontal cortex, a brain region critical for executive functions.
This mechanism differs from that of methylphenidate or amphetamine‑based stimulants, which increase dopamine and norepinephrine release. The gradual onset of action—typically noticeable after one to two weeks—makes Atogard a suitable option for maintenance therapy.
Dosage Guidelines
Dosage of Atogard must be individualized based on patient weight, symptom severity, and response to therapy. The usual starting dose for adults and children older than 6 years is 40 mg once daily, taken with or without food. After a minimum of one week, the dose may be increased to 80 mg per day, divided into morning and afternoon doses if needed. The maximum recommended daily dose is 100 mg.
For pediatric patients weighing less than 70 kg, the initial dose is typically 0.5 mg per kilogram of body weight, rounded to the nearest 10 mg increment. Dose adjustments should be made under the supervision of a qualified healthcare professional.
Patients should be instructed to swallow the tablet whole; crushing or chewing may alter the drug’s release characteristics.
Side Effects
Like all medications, Atogard can cause adverse effects. The most commonly reported side effects include:
- Nausea, upset stomach, or abdominal pain
- Decreased appetite
- Weight loss
- Fatigue or insomnia
- Mood swings, including irritability
Less frequent but clinically important side effects may involve:
- Elevated liver enzymes—periodic liver function testing is recommended
- Severe allergic reactions such as rash, itching, or swelling
- Changes in blood pressure or heart rate
- Suicidal thoughts or behaviors, particularly in young patients
Patients should contact their physician promptly if they experience any of these serious reactions.
For more information on side effect profiles, see Drugs.com.
Warnings and Precautions
Before initiating Atogard therapy, healthcare providers should assess:
- History of cardiovascular disease, including heart attacks or arrhythmias
- Family history of bipolar disorder or psychosis, as Atomoxetine may precipitate mania
- Current use of monoamine oxidase inhibitors (MAOIs) or other antidepressants
- Pregnancy or breastfeeding status
Atogard is classified as Pregnancy Category C; therefore, it should only be used if the potential benefit justifies the potential risk. Breastfeeding is not recommended while taking this medication.
Patients with a history of liver disease should undergo regular monitoring of hepatic enzymes. Caution is advised in individuals with renal impairment, as the drug is primarily excreted unchanged in the urine.
It is essential to store Atogard at room temperature, away from moisture and heat, and to keep it out of reach of children.
Frequently Asked Questions
- What is the typical onset of effect with Atogard 60 mg? Most patients begin to notice improvement in ADHD symptoms after 1–2 weeks of consistent daily dosing, with full therapeutic effect often observed after 4–6 weeks.
- Can Atogard be taken with food? Yes, Atogard can be taken with or without food. However, taking it with a meal may help reduce gastrointestinal discomfort.
- Is Atogard addictive? No, Atomoxetine is not a controlled substance and has a low potential for abuse or dependence, making it a suitable option for patients with a history of substance misuse.
- Do I need regular laboratory tests while on Atogard? Routine monitoring of liver enzyme levels is recommended, especially during the first few months of therapy, to detect any hepatic abnormalities early.
- Can I switch from a stimulant medication to Atogard? Transition should be done under medical supervision. A gradual taper of the stimulant may be recommended to avoid withdrawal symptoms and to assess the efficacy of Atomoxetine.
For more detailed information about Atomoxetine and ADHD treatment, reputable sources such as the National Institutes of Health (NIH), the U.S. Food and Drug Administration (FDA), and MedlinePlus provide evidence‑based guidance.
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