Viberzi Side Effects
Generic Name: eluxadoline
Note: This page contains side effects data for the generic drug eluxadoline. It is possible that some of the dosage forms included below may not apply to the brand name Viberzi.
More frequent side effects include: abdominal pain, constipation, lower abdominal pain, nausea, upper abdominal pain, and vomiting. See below for a comprehensive list of adverse effects.
For the Consumer
Applies to eluxadoline: oral tablet
As well as its needed effects, eluxadoline (the active ingredient contained in Viberzi) may cause unwanted side effects that require medical attention.
Major Side Effects
If any of the following side effects occur while taking eluxadoline, check with your doctor immediately:Rare
- darkened urine
- fast heartbeat
- loss of appetite
- pains in the stomach, side, or abdomen, possibly radiating to the back
- yellow eyes or skin
Minor Side Effects
Some eluxadoline side effects may not need any medical attention. As your body gets used to the medicine these side effects may disappear. Your health care professional may be able to help you prevent or reduce these side effects, but do check with them if any of the following side effects continue, or if you are concerned about them:Less common:
- Body aches or pain
- cough producing mucus
- difficulty with breathing
- ear congestion
- excess air or gas in the stomach or intestines
- full feeling
- loss of voice
- muscle aches
- passing gas
- pressure in the stomach
- sore throat
- stuffy or runny nose
- swelling of abdominal or stomach area
- tightness in the chest
- unusual tiredness or weakness
For Healthcare Professionals
Applies to eluxadoline: oral tablet
The most commonly reported adverse reactions included constipation, nausea, and abdominal pain.[Ref]
Common (1% to 10%): Constipation, nausea, abdominal pain, vomiting, abdominal distention, flatulence, viral gastroenteritis
Uncommon (0.1% to 1%): Sphincter of Oddi spasm, pancreatitis
Frequency not reported: Gastroesophageal reflux disease[Ref]
Sphincter of Oddi spasm occurred in 0.2% (n=807) and 0.8% (n=1032) of patients receiving 75 mg and 100 mg twice a day, respectively. Sphincter of Oddi spasm manifested as abdominal pain with lipase elevation of less than 3 times the upper limit of normal in 1 patient, and elevated hepatic enzymes associated with abdominal pain in the second patient. For the 8 patients taking 100 mg twice a day, sphincter of Oddi spasm manifested in 1 patient as pancreatitis and as elevated hepatic enzymes associated with abdominal pain in the other 7 patients. Of 1317 patients with a gallbladder, no patients experienced a sphincter of Oddi spasm, while 2 of 165 patients and 8 of 184 patients in the 75 mg and 100 mg twice a day groups, respectively, experienced sphincter of Oddi spasm. Onset of symptoms occurred within the first week in 80% (8 of 10) of patients and no cases occurred greater than 1 month after treatment onset. The 1 case of sphincter of Oddi spasm-induced pancreatitis occurred within minutes of taking the first dose of the drug and resolved within 24 hours of discontinuation.
Pancreatitis not associated with sphincter of Oddi spasm was reported in 0.2% (n=807) and 0.3% (n=1032) of patients receiving 75 mg and 100 mg twice a day, respectively. Of these 5 cases, 3 were associated with excessive alcohol intake, 1 with biliary sludge, and 1 was reported 2 weeks after the patient discontinued therapy. All resolved within 1 week of therapy discontinuation.
Constipation was the most commonly reported adverse event in clinical trials with 50% of case reported within the first 2 weeks, and the majority within the first 3 months. Rates of severe constipation were less than 1%. After 3 months, the incidence of constipation was similar across active treatment and placebo groups.
Gastroesophageal reflux disease was reported in 2% or less of patients in clinical trials.[Ref]
Increased AST was reported in 2% or less of patients in clinical trials.[Ref]
Frequency not reported: Increased AST[Ref]
Common (1% to 10%): Upper respiratory tract infection, nasopharyngitis, bronchitis
Frequency not reported: Asthma, bronchospasm, respiratory failure, wheezing[Ref]
Asthma, bronchospasm, respiratory failure, and wheezing were reported in 2% or less of patients in clinical trials.[Ref]
Common (1% to 10%): Rash[Ref]
Rash included terms such as dermatitis, dermatitis allergic, rash, rash erythematous, rash generalized, rash maculopapular, rash popular, rash pruritic, urticaria, and idiopathic urticaria.[Ref]
Common (1% to 10%): Dizziness
Frequency not reported: Sedation, somnolence[Ref]
Sedation and somnolence was reported in 2% or less of patients in clinical trials.[Ref]
Euphoric mood was reported in 2% or less of patients in clinical trials.[Ref]
Frequency not reported: Euphoric mood[Ref]
Feeling drunk was reported in 2% or less of patients in clinical trials.[Ref]
Common (1% to 10%): Fatigue
Frequency not reported: Feeling drunk[Ref]
1. "Product Information. Viberzi (eluxadoline)." Actavis Pharma, Inc., Parsippany, NJ.
It is possible that some side effects of Viberzi may not have been reported. These can be reported to the FDA here. Always consult a healthcare professional for medical advice.
More about Viberzi (eluxadoline)
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