Cotempla XR ODT (methylphenidate ER) is a stimulant medication. It's approved for children ages 6 to 17 years old with ADHD (attention deficit-hyperactivity disorder). Cotempla XR ODT (methylphenidate ER) comes as an orally disintegrating tablet (ODT) that's dissolved on the tongue once per day in the morning. Side effects include low appetite and trouble sleeping.
Cotempla XR ODT (methylphenidate ER) is a stimulant medication. It's not exactly known how the medication helps to improve attention and focus. But it's thought to workby raising the levels of chemicals in your brain called norepinephrine, dopamine, and serotonin.
Cotempla XR ODT (methylphenidate ER) can cause some serious health issues. This risk may be even higher for certain groups. If this worries you, talk to your doctor or pharmacist about other options.
Cotempla XR ODT (methylphenidate ER) has a risk for misuse and addiction. Misuse is when a medication is used differently than how it's prescribed. Misusing Cotempla XR ODT (methylphenidate ER) can raise the risk for serious side effects such as fast heart rate, high blood pressure, aggressive behavior, and even thoughts of hurting yourself. In addition, misusing Cotempla XR ODT (methylphenidate ER) can sometimes lead to addiction. Your child should take this medication exactly as prescribed to them. Speak with your child's prescriber if you're concerned about this risk.
Because of the risk for misuse and addiction, store Cotempla XR ODT (methylphenidate ER) in a safe place out of reach from children, pets, and visitors. Don't give the medication to anyone else. If your child no longer needs Cotempla XR ODT (methylphenidate ER), safely get rid of the medication through a take-back program.
Taking Cotempla XR ODT (methylphenidate ER) for a long period of time can put people at risk for dependence. This means that over time, people can become physically dependent on the medication to function normally. Physical dependence is usually related to having withdrawal symptoms, like irritability, nightmares, and sleep problems, if people take the medication for a long time and then suddenly stop or suddenly lower the dose. Make sure your child takes Cotempla XR ODT (methylphenidate ER) exactly as prescribed. Don't change the dose or how often they take it without talking to the prescriber first.
There have been reports of sudden death and heart attack in people with a heart condition who took stimulant medications like Cotempla XR ODT (methylphenidate ER) at usual doses. This medication can also raise blood pressure and heart rate.
Tell your child's prescriber if your child has a history of heart problems before treatment starts to make sure Cotempla XR ODT (methylphenidate ER) is safe to take. Your child's prescriber will check for heart problems before starting treatment. Your child might not be able to take Cotempla XR ODT (methylphenidate ER) if they have serious heart problems.
Let your child's prescriber or primary care provider know if your child experiences unexplained fainting, chest pain with physical activity, or irregular heartbeat during treatment with Cotempla XR ODT (methylphenidate ER). The care team can check your child's heart to make sure everything is okay.
Some people who've taken a stimulant like Cotempla XR ODT (methylphenidate ER) can have mental health problems, such as hallucinations (seeing things that aren't really there), aggressive behavior, unclear thinking, and mania. This medication can worsen mood-related problems that your child already has, but these changes in behavior can also happen even if they haven't had these problems before. Talk to your child's prescriber right away if your child develops these mood or behavior changes during treatment with Cotempla XR ODT (methylphenidate ER). Your child might have to stop the medication.
In studies, stimulants like Cotempla XR ODT (methylphenidate ER) slowed the growth rate (both in height and weight) and caused weight loss in children. Let your child's pediatrician or primary care provider know that your child is taking Cotempla XR ODT (methylphenidate ER). They'll need to check your child's growth progress closely. Your child might need to briefly stop or completely stop taking Cotempla XR ODT (methylphenidate ER) if there's a possibility of any slowed growth that's happened. Talk to your child's primary care provider if you have any concerns.
Cotempla XR ODT (methylphenidate ER) might be linked to poor blood circulation problems, such as Raynaud's phenomenon. People with Raynaud's phenomenon can have episodes of poor blood flow in the fingers and toes, which can cause the skin to turn pale and to feel cold, numb, or painful. Symptoms are usually mild. But in some rare and more serious cases, it can cause sores or ulcers. Let your child's prescriber know if your child complains about instances of numbness or pain in the fingers or toes. Your child's prescriber might need to lower the Cotempla XR ODT (methylphenidate ER) dose or consider a different medication.
Although rare, some people who took methylphenidate medications like Cotempla XR ODT (methylphenidate ER) reported developing higher pressure in the eyes, which can lead to glaucoma. Make sure your child visits their optometrist for regular eye exams. Speak with the optometrist if your child reports any changes in vision during treatment.
Cotempla XR ODT (methylphenidate ER) can interact with many medications. For example, Cotempla XR ODT (methylphenidate ER) can counteract (work against) the effects of many blood pressure medications. This means that blood pressure medications might not work as well if they're taken with Cotempla XR ODT (methylphenidate ER). Additionally, taking Cotempla XR ODT (methylphenidate ER) with monoamine oxidase inhibitors (MAOIs) can raise the risk of having severely high blood pressure, so it's best to avoid this combination.
Discuss with your child's care team about all the medications they take (including over-the-counter medications and supplements) before and during treatment with Cotempla XR ODT (methylphenidate ER).
The following side effects may get better over time as your body gets used to the medication. Let your healthcare provider know immediately if you continue to experience these symptoms or if they worsen over time.
Contact your healthcare provider immediately if you experience any of the following.
Side effects that you should report to your care team as soon as possible:
Side effects that usually do not require medical attention (report these to your care team if they continue or are bothersome):
Yes, Cotempla XR ODT (methylphenidate ER) is a stimulant medication that's used to treat ADHD in children ages 6 to 17 years. Although stimulants like Cotempla XR ODT (methylphenidate ER) work well for ADHD, they generally have many possible side effects and safety warnings. So it's best to discuss with the prescriber about the risks that come with taking Cotempla XR ODT (methylphenidate ER) and whether it's an appropriate ADHD treatment option for your child.
Cotempla XR ODT (methylphenidate ER) starts to work within an hour to help treat ADHD symptoms. Speak with your child's prescriber if you have concerns about how quickly the medication seems to kick in for your child.
The effects of Cotempla XR ODT (methylphenidate ER) can last for up to 12 hours after a single dose. For this reason, your child should take Cotempla XR ODT (methylphenidate ER) in the morning so the medication can help with ADHD symptoms during the day. Taking it later on in the day might make your child have trouble sleeping at night.
It takes almost a day for most of Cotempla XR ODT (methylphenidate ER) to leave the body after a single dose. This time frame is estimated based on the half-life of Cotempla XR ODT (methylphenidate ER). Talk with your child's healthcare team if you have specific concerns about how long this medication might stay in your child's body.
No, don't break Cotempla XR ODT (methylphenidate ER) tablets in half. Orally dissolving tablets like Cotempla XR ODT (methylphenidate ER) are delicate and they break or dissolve easily. The tablet might suddenly break into much smaller pieces if you try to break it. The tablet also isn't scored, meaning that it doesn't have an indented line on it to help you break the tablet evenly. This can cause your child to take the wrong dose.
Cotempla XR ODT (methylphenidate ER) is FDA-approved for children ages 6 to 17 years old only. It's not recommended for adults to take Cotempla XR ODT (methylphenidate ER) because it's not known how well this medication will work for adults. Additionally, studies show that methylphenidate products, like Cotempla XR ODT (methylphenidate ER), might not work as well as amphetamine medications, like Adderall, for adults with ADHD. Speak with your prescriber about your options if you're looking for an ADHD medication that's available for adults.
Cotempla XR ODT (methylphenidate ER) is made by a pharmaceutical manufacturer called Aytu BioPharma.
| Dosage | Quantity | Price as low as | Price per unit |
|---|---|---|---|
| 8.6mg | 30 orally disintegrating tabs | $411.63 | $13.72 |
| 17.3mg | 30 orally disintegrating tabs | $411.63 | $13.72 |
| 25.9mg | 30 orally disintegrating tabs | $411.63 | $13.72 |
The typical starting dose is 17.3 mg dissolved on the tongue once daily in the morning. Your child's prescriber will adjust the dose after a week depending on how well the medication is working. The maximum dose is 51.8 mg once daily.
Contraindications are specific health conditions or situations in which a person should not take a medication due to safety concerns. If you have any of the following conditions or if any of the following apply to you, let your healthcare provider know because Cotempla XR ODT (methylphenidate ER) will not be safe for you to take.