Cotempla XR-ODT (methylphenidate orally disintegrating tablet)

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Cotempla XR-ODT is the first extended-release orally disintegrating tablet (ODT) specifically designed for the treatment of ADHD in pediatric patients. Unlike traditional pills that must be swallowed or chewed, this medication dissolves quickly on the tongue without the need for water, making it an ideal solution for children who struggle with swallowing capsules. It utilizes a specialized microparticle technology to provide a steady release of methylphenidate throughout the day, offering a balance of immediate focus and sustained symptom control for up to 12 hours.

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Cotempla XR-ODT

Cotempla XR-ODT is a stimulant medication used to treat attention deficit hyperactivity disorder (ADHD) in children. It contains a central nervous system (CNS) stimulant called methylphenidate.

What Are Side Effects of Cotempla XR ODT?

Cotempla XR ODT may cause serious side effects including:

coldness in the fingers or toes,
numbness or pain in the fingers or toes,
skin color changes in the fingers or toes,
unusual wounds on the fingers or toes,
fast, pounding or irregular heartbeats,v
mood changes,
agitation,
aggression,
mood swings,
abnormal thoughts,
thoughts of suicide,
uncontrolled muscle movements,
sudden outbursts of words or sounds,
blurred vision,
fainting,
seizure,
chest pain,
jaw or left arm pain,
shortness of breath,
unusual sweating,
weakness on one side of the body,
trouble speaking,
confusion,
vision changes,
painful or prolonged penis erection lasting over 4 hours,
rash,
itching,
swelling of the face, tongue, or throat,
severe dizziness, and
trouble breathing

Get medical help right away, if you have any of the symptoms listed above.

Common side effects of Cotempla XR-ODT include:

Seek medical care or call 911 at once if you have the following serious side effects:

Serious eye symptoms such as sudden vision loss, blurred vision, tunnel vision, eye pain or swelling, or seeing halos around lights;
Serious heart symptoms such as fast, irregular, or pounding heartbeats; fluttering in your chest; shortness of breath; and sudden dizziness, lightheadedness, or passing out;
Severe headache, confusion, slurred speech, arm or leg weakness, trouble walking, loss of coordination, feeling unsteady, very stiff muscles, high fever, profuse sweating, or tremors.

This document does not contain all possible side effects and others may occur. Check with your physician for additional information about side effects.

Dosage for Cotempla XR ODT

The recommended starting dose of Cotempla XR-ODT for pediatric patients 6 to 17 years of age is 17.3 mg given orally once daily in the morning. Dosage may be increased weekly in increments of 8.6 mg to 17.3 mg per day.

What Drugs, Substances, or Supplements Interact with Cotempla XR ODT?

Cotempla XR-ODT may interact with monoamine oxidase inhibitors (MAOIs), H2-blockers, and proton pump inhibitors (PPIs). Tell your doctor all medications and supplements you use.

Cotempla XR ODT During Pregnancy and Breastfeeding

Tell your doctor if you are pregnant or plan to become pregnant before using Cotempla XR-ODT; it is unknown how it may affect a fetus. There is a pregnancy exposure registry that monitors pregnancy outcomes in women exposed to Cotempla XR-ODT during pregnancy. It is believed Cotempla XR-ODT passes into breast milk. Consult your doctor before breastfeeding. Withdrawal symptoms may occur if you suddenly stop taking Cotempla XR-ODT.

Additional Information

Our Cotempla XR-ODT (methylphenidate extended-release orally disintegrating tablets) Side Effects Drug Center provides a comprehensive view of available drug information on the potential side effects when taking this medication.