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Oxtellar XR

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Oxtellar XR

Oxtellar XR

Oxtellar XR Side Effects Center

Medical Editor: John P. Cunha, DO, FACOEP

Oxtellar XR (oxcarbazepine) in an antieleptic drug (AED) used as an additional therapy as part of treatment for partial seizures in adults and children ages 6 to 17. Oxtellar XR is an anticonvulsant. It is available in generic form. Common side effects include dizziness, sleepiness, headache, balance problems, double vision, tremor, weakness, fatigue, and vomiting.

The recommended daily dose of Oxtellar XR is 1,200 mg to 2,400 mg per day. Adults should begin with 600 mg per day, with weekly dose increases of 600 mg until the recommended daily dose is achieved. Dosing in children is based on weight. Hormonal contraceptives, Dilantin (phenytoin), Tegretol (carbamazepine), Carbatrol (carbamazepine), Equetro (carbamazepine), and Phenobarbital may interact with Oxtellar XP. Oxtellar XR may cause harm to a fetus. Women who are pregnant or are planning to become pregnant should talk with their doctors to decide whether or not to take Oxtellar XR while pregnant. Oxtellar XR passes into breast milk. Nursing mothers should discuss with their doctors whether to take Oxtellar XR or breastfeed. Nursing mothers should not do both. Stopping Oxtellar XR suddenly can cause serious problems, including seizures.

Our Oxtellar XR (oxcarbazepine) Side Effects Drug Center provides a comprehensive view of available drug information on the potential side effects when taking this medication.

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

What is Prescribing information?

The FDA package insert formatted in easy-to-find categories for health professionals and clinicians.

Oxtellar XR FDA Prescribing Information: Side Effects
(Adverse Reactions)

SIDE EFFECTS

The following adverse reactions are described in other sections of the labeling:

Clinical Trials Experience

Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in clinical practice.

The safety data presented below are from 384 patients with partial epilepsy who received Oxtellar XR™ (366 adults and 18 children) with concomitant AEDs.

In addition, safety data presented below are from a total of 2,288 patients with seizure disorders treated with immediate-release oxcarbazepine; 1,832 were adults and 456 were children.

Most Common Adverse Reactions Reported by Adult Patients Receiving Concomitant AEDs in Oxtellar XR™ Clinical Studies

Table 3 lists adverse reactions that occurred in at least 2% of adult patients with epilepsy treated with Oxtellar XR™ or placebo and concomitant AEDs and that were numerically more common in the patients treated with any dose of Oxtellar XR™ than in patients receiving placebo.

The overall incidence of adverse reactions appeared to be dose related, particularly during the Titration Period. The most commonly observed ( ≥ 5%) adverse reactions seen in association with Oxtellar XR™ and more frequent than in placebo-treated patients were: dizziness, somnolence, headache, balance disorder, tremor, vomiting, diplopia, and asthenia.

Table 3: Adverse Reaction Incidence in a Controlled Clinical Study of Oxtellar XR™ with Concomitant AEDs in Adults*

  Oxtellar XR 2400 mg/day
N=123
%
Oxtellar XR 1200 mg/day
N=122
%
Placebo
N=121
%
Any System / Any Term 69 57 55
Nervous System Disorders
  Dizziness 41 20 15
  Somnolence 14 12 9
  Headache 15 8 7
  Balance Disorder 7 5 5
  Tremor 1 5 2
  Nystagmus 3 3 1
  Ataxia 1 3 1
Gastrointestinal Disorders
  Vomiting 15 6 9
  Abdominal Pain Upper 0 3 1
  Dyspepsia 0 3 1
  Gastritis 0 3 2
Eye Disorders
  Diplopia 13 10 4
  Vision Blurred 1 4 3
  Visual Impairment 1 3 0
General Disorders And Administration Site Conditions
  Asthenia 7 3 1
  Fatigue 3 6 1
  Gait Disturbance 0 3 1
  Drug Intolerance 2 0 0
Infections And Infestations
  Nasopharyngitis 0 3 0
  Sinusitis 0 3 2
* Reported by ≥ 2% of Patients Treated with Oxtellar XR™ and Numerically More Frequent than in the Placebo Group

Adverse Reactions Associated with Discontinuation of Oxtellar XR™ Treatment

Approximately 23.3% of the 366 adult patients receiving Oxtellar XR™ in clinical studies discontinued treatment because of an adverse reaction. The adverse reactions most commonly associated with discontinuation of Oxtellar XR™ (reported by ≥ 2%) were: dizziness (9.8%), vomiting (5.3%), nausea (3.7%), diplopia (3.2%), and somnolence (2.4%).

Adjunctive Therapy with Oxtellar XR™ in Pediatric Patients 4 to 16 Years Old Previously Treated with other AEDs

In a pharmacokinetic study in 18 children (age 4-16 years) with partial seizures treated with different doses of Oxtellar XR™, the observed adverse reactions seen in association with Oxtellar XR™ were similar to those seen in adults.

Most Common Adverse Reactions in Immediate-Release Oxcarbazepine Controlled Clinical Studies

Controlled Clinical Studies of Adjunctive Therapy with Immediate-Release Oxcarbazepine in Adults Previously Treated with other AEDs: Table 4 lists adverse reactions that occurred in at least 2% of adult patients with epilepsy treated with immediate-release oxcarbazepine or placebo with concomitant AEDs and that were numerically more common in the patients treated with any dose of immediate-release oxcarbazepine than in placebo. As immediate-release oxcarbazepine and Oxtellar XR™ were not examined in the same trial, adverse event frequencies cannot be directly compared between the two formulations.

Table 4: Adverse Reaction Incidence in a Controlled Clinical Study of Immediate Release Oxcarbazepine with Concomitant AEDs in Adults*

  Immediate-Release Oxcarbazepine Dosage (mg/day) Placebo
N = 166 %
OXC 600
N = 163 %
OXC 1200
N = 171 %
OXC 2400
N = 126 %
Body as a Whole
  Fatigue 15 12 15 7
  Asthenia 6 3 6 5
  Edema Legs 2 1 2 1
  Weight Increase 1 2 2 1
  Feeling Abnormal 0 1 2 0
Cardiovascular System
  Hypotension 0 1 2 0
Digestive System
  Nausea 15 25 29 10
  Vomiting 13 25 36 5
  Pain Abdominal 10 13 11 5
  Diarrhea 5 6 7 6
  Dyspepsia 5 5 6 2
  Constipation 2 2 6 4
  Gastritis 2 1 2 1
Metabolic and Nutritional Disorders
  Hyponatremia 3 1 2 1
Musculoskeletal System
  Muscle Weakness 1 2 2 0
  Sprains and Strains 0 2 2 1
Nervous System
  Headache 32 28 26 23
  Dizziness 36 32 49 13
  Somnolence 20 28 36 12
  Ataxia 9 17 31 5
  Nystagmus 7 20 26 5
  Gait Abnormal 5 10 17 1
  Insomnia 4 2 3 1
  Tremor 3 8 16 5
  Nervousness 2 4 2 1
  Agitation 1 1 2 1
  Coordination Abnormal 1 3 2 1
  EEG Abnormal 0 0 2 0
  Speech Disorder 1 1 3 0
  Confusion 1 1 2 1
  Cranial Injury NOS 1 0 2 1
  Dysmetria 1 2 3 0
  Thinking Abnormal 0 2 4 0
Respiratory System
  Rhinitis 2 4 5 4
Skin and Appendages
  Acne 1 2 2 0
Special Senses
  Diplopia 14 30 40 5
  Vertigo 6 12 15 2
  Vision Abnormal 6 14 13 4
  Accommodation Abnormal 0 0 2 0
* Events in at Least 2% of Patients Treated with 2400mg/day of Immediate-Release Oxcarbazepine and Numerically More Frequent than in the Placebo Group

Other Reactions Observed in Association with the Administration of Immediate-Release Oxcarbazepine

In the paragraphs that follow, the adverse reactions, other than those in the preceding tables or text, that occurred in a total of 565 children and 1,574 adults exposed to immediate-release oxcarbazepine and that are reasonably likely to be related to drug use are presented. Events common in the population, events reflecting chronic illness and events likely to reflect concomitant illness are omitted particularly if minor. They are listed in order of decreasing frequency. Because the reports cite reactions observed in open label and uncontrolled trials, the role of immediate-release oxcarbazepine in their causation cannot be reliably determined.

Body as a Whole: fever, malaise, pain chest precordial, rigors, weight decrease.

Cardiovascular System: bradycardia, cardiac failure, cerebral hemorrhage, hypertension, hypotension postural, palpitation, syncope, tachycardia.

Digestive System: appetite increased, blood in stool, cholelithiasis, colitis, duodenal ulcer, dysphagia, enteritis, eructation, esophagitis, flatulence, gastric ulcer, gingival bleeding, gum hyperplasia, hematemesis, hemorrhage rectum, hemorrhoids, hiccup, mouth dry, pain biliary, pain right hypochondrium, retching, sialoadenitis, stomatitis, stomatitis ulcerative.

Hematologic and Lymphatic System: thrombocytopenia.

Laboratory Abnormality: gamma-GT increased, hyperglycemia, hypocalcemia, hypoglycemia, hypokalemia, liver enzymes elevated, serum transaminase increased.

Musculoskeletal System: hypertonia muscle.

Nervous System: aggressive reaction, amnesia, anguish, anxiety, apathy, aphasia, aura, convulsions aggravated, delirium, delusion, depressed level of consciousness, dysphonia, dystonia, emotional lability, euphoria, extrapyramidal disorder, feeling drunk, hemiplegia, hyperkinesia, hyperreflexia, hypoesthesia, hypokinesia, hyporeflexia, hypotonia, hysteria, libido decreased, libido increased, manic reaction, migraine, muscle contractions involuntary, nervousness, neuralgia, oculogyric crisis, panic disorder, paralysis, paroniria, personality disorder, psychosis, ptosis, stupor, tetany.

Respiratory System: asthma, bronchitis, coughing, dyspnea, epistaxis, laryngismus, pleurisy.

Skin and Appendages: acne, alopecia, angioedema, bruising, dermatitis contact, eczema, facial rash, flushing, folliculitis, heat rash, hot flushes, photosensitivity reaction, pruritus genital, psoriasis, purpura, rash erythematous, rash maculopapular, vitiligo, urticaria.

Special Senses: accommodation abnormal, cataract, conjunctival hemorrhage, edema eye, hemianopia, mydriasis, otitis externa, photophobia, scotoma, taste perversion, tinnitus, xerophthalmia.

Urogenital and Reproductive System: dysuria, hematuria, intermenstrual bleeding, leukorrhea, menorrhagia, micturition frequency, pain renal, pain urinary tract, polyuria, priapism, renal calculus, urinary tract infection.

Other: Systemic lupus erythematosus.

Postmarketing and Other Experience

The following adverse reactions have been identified during post-approval use of immediate-release oxcarbazepine. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.

Body as a Whole: multi-organ hypersensitivity disorders characterized by features such as rash, fever, lymphadenopathy, abnormal liver function tests, eosinophilia and arthralgia [see WARNINGS AND PRECAUTIONS]

Anaphylaxis: [see WARNINGS AND PRECAUTIONS]

Digestive System: pancreatitis and/or lipase and/or amylase increase

Hematologic and Lymphatic Systems: aplastic anemia [see WARNINGS AND PRECAUTIONS]

Skin and Appendages: erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis [see WARNINGS AND PRECAUTIONS]

Read the entire FDA prescribing information for Oxtellar XR (Oxcarbazepine Extended-Release Tablets) »

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Report Problems to the Food and Drug Administration

 

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.


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