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Nucynta Patient Information including How Should I Take
In this Article
- What is tapentadol (Nucynta)?
- What are the possible side effects of tapentadol (Nucynta)?
- What is the most important information I should know about tapentadol (Nucynta)?
- What should I discuss with my healthcare provider before taking tapentadol (Nucynta)?
- How should I take tapentadol (Nucynta)?
- What happens if I miss a dose (Nucynta)?
- What happens if I overdose (Nucynta)?
- What should I avoid while taking tapentadol (Nucynta)?
- What other drugs will affect tapentadol (Nucynta)?
- Where can I get more information?
What should I discuss with my healthcare provider before taking tapentadol (Nucynta)?
You should not use this medication if you are allergic to tapentadol, or if you have severe liver or kidney disease, if you are having an asthma attack, or if you have a bowel obstruction called paralytic ileus.
Do not use tapentadol if you have used an MAO inhibitor such as furazolidone (Furoxone), isocarboxazid (Marplan), phenelzine (Nardil), rasagiline (Azilect), selegiline (Eldepryl, Emsam, Zelapar), or tranylcypromine (Parnate) in the last 14 days. A dangerous drug interaction could occur, leading to serious side effects.
To make sure you can safely take tapentadol, tell your doctor if you have any of these other conditions:
- asthma, COPD, sleep apnea, or other breathing disorders;
- liver or kidney disease;
- curvature of the spine;
- a history of head injury or brain tumor;
- epilepsy or other seizure disorder;
- gallbladder disease or pancreas problems;
- mental illness; or
- a history of drug or alcohol addiction.
FDA pregnancy category C. It is not known whether this medication is harmful to an unborn baby. Tapentadol may cause breathing problems and addiction or withdrawal symptoms in a newborn if the mother takes the medication during pregnancy. Tell your doctor if you are pregnant or plan to become pregnant during treatment.
Tapentadol can pass into breast milk and may harm a nursing baby. Do not breast-feed while taking this medication.
Older adults may be more sensitive to the effects of this medicine.
Tapentadol may be habit forming and should be used only by the person it was prescribed for. Never share tapentadol with another person, especially someone with a history of drug abuse or addiction. Keep the medication in a place where others cannot get to it.
Do not give tapentadol to a child.
How should I take tapentadol (Nucynta)?
Take exactly as prescribed. Never take tapentadol in larger amounts, or for longer than recommended by your doctor. Follow the directions on your prescription label. Tell your doctor if the medicine seems to stop working as well in relieving your pain.
Your doctor may occasionally change the timing of your dose to make sure you get the best results.
Take this medicine with a full glass of water. Tapentadol can be taken with or without food.
Do not crush, chew, or break an extended-release tablet. Swallow it whole. Breaking or opening the pill may cause too much of the drug to be released at one time.
Tapentadol can cause constipation. Talk to your doctor before using a laxative or stool softener to treat or prevent this side effect.
Do not stop using tapentadol suddenly, or you could have unpleasant withdrawal symptoms. Ask your doctor how to avoid withdrawal symptoms when you stop using tapentadol.
Store at room temperature away from moisture and heat.
Keep track of the amount of medicine used from each new bottle. Tapentadol is a drug of abuse and you should be aware if anyone is using your medicine improperly or without a prescription.
After you have stopped using this medication, flush any unused pills down the toilet.
Never crush a tablet or other pill to mix into a liquid for snorting tapentadol or injecting the drug into your vein. This practice has resulted in death with the misuse of narcotic pain medicines and similar prescription drugs.
Additional Nucynta Information
- Nucynta Drug Interactions Center: tapentadol oral
- Nucynta Side Effects Center
- Nucynta FDA Approved Prescribing Information including Dosage
Report Problems to the Food and Drug Administration
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