openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings sections page 1 of 1 · 1 matching rows.
warnings and cautions
5 WARNINGS AND PRECAUTIONS Periodically reevaluate the benefit and potential for adverse effects such as worsening mood, cognition, rigidity, and functional capacity ( 5.1 ) Do not exceed 50 mg/day and the maximum single dose should not exceed 25 mg if administered in conjunction with a strong CYP2D6 inhibitor (e .g, fluoxetine, paroxetine) ( 5.3 , 7.1 ) Neuroleptic Malignant Syndrome (NMS): Discontinue if this occurs ( 5.4 , 7.6 ) Restlessness, agitation, akathisia and parkinsonism: Reduce dose or discontinue if occurs ( 5.5 , 5.6 ) Dysphagia and aspiration pneumonia: Monitor for dysphagia ( 5.7 ) Sedation/Somnolence: May impair patient's ability to drive or operate complex machinery ( 5.8 ) QTc prolongation: Not recommended in combination with other drugs that prolong QTc ( 5.9 ) Exaggerate extrapyramidal disorders when used with drugs that reduce or antagonize dopamine. Discontinue Tetrabenazine tablet if this occurs ( 5.12 ) 5.1 Clinical Worsening and Adverse Effects Huntington's disease is a progressive disorder characterized by changes in mood, cognition, chorea, rigidity, and functional capacity over time. In a 12-week controlled trial, Tetrabenazine tablet was also shown to cause slight worsening in mood, cognition, rigidity, and functional capacity. Whether these effects persist, resolve, or worsen with continued treatment is unknown. Prescribers should periodically re-evaluate the need for Tetrabenazine tablet in their patients by assessing the beneficial effect on chorea and possible adverse effects, including depression, cognitive decline, parkinsonism, dysphagia, sedation/somnolence, akathisia, restlessness and disability. It may be difficult to distinguish between drug-induced side-effects and progression of the underlying disease; decreasing the dose or stopping the drug may help the clinician distinguish between the two possibilities. In some patients, underlying chorea itself may improve over time, decreasing the need for Tetrabenazine tablet. 5.2 Depression and Suicidality Patients with Huntington's disease are at increased risk for depression, suicidal ideation or behaviors (suicidality). Tetrabenazine tablet increases the risk for suicidality in patients with HD. All patients treated with Tetrabenazine tablet should be observed for new or worsening depression or suicidality. If depression or suicidality does not resolve, consider discontinuing treatment with Tetrabenazine tablet. In a 12-week, double-blind placebo-controlled study in patients with chorea associated with Huntington's disease, 10 of 54 patients (19%) treated with Tetrabenazine tablet were reported to have an adverse event of depression or worsening depression compared to none of the 30 placebo-treated patients. In two open-label studies (in one study, 29 patients received Tetrabenazine tablet for up to 48 weeks; in the second study, 75 patients received Tetrabenazine tablet for up to 80 weeks), the rate of depression/worsening depression was 35%. In all of the HD chorea studies of Tetrabenazine tablet (n=187), one patient committed suicide, one attempted suicide, and six had suicidal ideation. Clinicians should be alert to the heightened risk of suicide in patients with Huntington's disease regardless of depression indices. Reported rates of completed suicide among individuals with Huntington's disease ranged from 3-13% and over 25% of patients attempt suicide at some point in their illness. Patients, their caregivers, and families should be informed of the risks of depression, worsening depression, and suicidality associated with Tetrabenazine tablet and should be instructed to report behaviors of concern promptly to the treating physician. Patients with HD who express suicidal ideation should be evaluated immediately 5.3 Laboratory Tests Before prescribing a daily dose of Tetrabenazine tablet that is greater than 50 mg per day, patients should be genotyped to determine if they express the drug metabolizing enzyme, CYP2D6. CYP2D6 testing is necessary to determine whether patients are poor metabolizers (PMs), extensive (EMs) or intermediate metabolizers (IMs) of Tetrabenazine tablet. Patients who are PMs of Tetrabenazine tablet will have substantially higher levels of the primary drug metabolites (about 3-fold for α-HTBZ and 9-fold for β-HTBZ) than patients who are EMs. The dosage should be adjusted according to a patient's CYP2D6 metabolizer status. In patients who are identified as CYP2D6 PMs, the maximum recommended total daily dose is 50 mg and the maximum recommended single dose is 25 mg [see Dosage and Administration (2.2) , Use in Specific Populations (8.7) , and Clinical Pharmacology (12.3) ]. 5.4 Neuroleptic Malignant Syndrome (NMS) A potentially fatal symptom complex sometimes referred to as Neuroleptic Malignant Syndrome (NMS) has been reported in association with Tetrabenazine tablet and other drugs that reduce dopaminergic transmission [see Warnings and Precautions (5.12) and Drug Interactions (7.6) ]. Clinical manifestations of NMS are hyperpyrexia, muscle rigidity, altered mental status, and evidence of autonomic instability (irregular pulse or blood pressure, tachycardia, diaphoresis, and cardiac dysrhythmia). Additional signs may include elevated creatinine phosphokinase, myoglobinuria, rhabdomyolysis, and acute renal failure. The diagnosis of NMS can be complicated; other serious medical illness (e.g., pneumonia, systemic infection), and untreated or inadequately treated extrapyramidal disorders can present with similar signs and symptoms. Other important considerations in the differential diagnosis include central anticholinergic toxicity, heat stroke, drug fever, and primary central nervous system pathology. The management of NMS should include (1) immediate discontinuation of Tetrabenazine tablet and other drugs not essential to concurrent therapy; (2) intensive symptomatic treatment and medical monitoring; and (3) treatment of any concomitant serious medical problems for which specific treatments are available. There is no general agreement about specific pharmacological treatment regimens for NMS. Recurrence of NMS has been reported. If treatment with Tetrabenazine tablet is needed after recovery from NMS, patients should be monitored for signs of recurrence. 5.5 Akathisia, Restlessness, and Agitation In a 12-week, double-blind, placebo-controlled study in patients with chorea associated with HD, akathisia was observed in 10 (19%) of Tetrabenazine tablet-treated patients and 0% of placebo-treated patients. In an 80-week open-label study, akathisia was observed in 20% of Tetrabenazine tablet-treated patients. Akathisia was not observed in a 48-week open-label study. Patients receiving Tetrabenazine tablet should be monitored for the presence of akathisia. Patients receiving Tetrabenazine tablet should also be monitored for signs and symptoms of restlessness and agitation, as these may be indicators of developing akathisia. If a patient develops akathisia, the Tetrabenazine tablet dose should be reduced; however, some patients may require discontinuation of therapy. 5.6 Parkinsonism Tetrabenazine tablet can cause parkinsonism. In a 12-week double-blind, placebo-controlled study in patients with chorea associated with HD, symptoms suggestive of parkinsonism (i.e., bradykinesia, hypertonia and rigidity) were observed in 15% of Tetrabenazine tablet-treated patients compared to 0% of placebo-treated patients. In 48-week and 80-week open-label studies, symptoms suggestive of parkinsonism were observed in 10% and 3% of Tetrabenazine tablet-treated patients, respectively. Because rigidity can develop as part of the underlying disease process in Huntington's disease, it may be difficult to distinguish between this drug-induced side-effect and progression of the underlying disease process. Drug-induced parkinsonism has the potential to cause more functional disability than untreated chorea for some patients with Huntington's disease. If a patient develops parkinsonism during treatment with Tetrabenazine tablet, dose reduction should be considered; in some patients, discontinuation of therapy may be necessary. 5.7 Dysphagia Dysphagia is a component of HD. However, drugs that reduce dopaminergic transmission have been associated with esophageal dysmotility and dysphagia. Dysphagia may be associated with aspiration pneumonia. In a 12-week, double-blind, placebo-controlled study in patients with chorea associated with HD, dysphagia was observed in 4% of Tetrabenazine tablet-treated patients and 3% of placebo-treated patients. In 48-week and 80-week open-label studies, dysphagia was observed in 10% and 8% of Tetrabenazine tablet-treated patients, respectively. Some of the cases of dysphagia were associated with aspiration pneumonia. Whether these events were related to treatment is unknown. 5.8 Sedation and Somnolence Sedation is the most common dose-limiting adverse reaction of Tetrabenazine tablet. In a 12-week, double-blind, placebo-controlled trial in patients with chorea associated with HD, sedation/somnolence occured in 17/54 (31%) Tetrabenazine tablet-treated patients and in 1 (3%) placebo-treated patient. Sedation was the reason upward titration of Tetrabenazine tablet was stopped and/or the dose of Tetrabenazine tablet was decreased in 15/54 (28%) patients. In all but one case, decreasing the dose of Tetrabenazine tablet resulted in decreased sedation. In 48-week and 80-week open-label studies, sedation/ somnolence occured in 17% and 57% of Tetrabenazine tablet-treated patients, respectively. In some patients, sedation occurred at doses that were lower than recommended doses. Patients should not perform activities requiring mental alertness to maintain the safety of themselves or others, such as operating a motor vehicle or operating hazardous machinery, until they are on a maintenance dose of Tetrabenazine tablet and know how the drug affects them. 5.9 QTc Prolongation Tetrabenazine tablet causes a small increase (about 8 msec) in the corrected QT (QTc) interval. QT prolongation can lead to development of torsade de pointes-type ventricular tachycardia with the risk increasing as the degree of prolongation increases [ see Clinical Pharmacology (12.2) ]. The use of Tetrabenazine tablet should be avoided in combination with other drugs that are known to prolong QTc, including antipsychotic medications (e.g., chlorpromazine, haloperidol, thioridazine, ziprasidone), antibiotics (e.g., moxifloxacin), Class 1A (e.g., quinidine, procainamide), and Class III (e.g., amiodarone, sotalol) antiarrhythmic medications or any other medications known to prolong the QTc interval [see Drug Interactions (7.5) ]. Tetrabenazine tablet should also be avoided in patients with congenital long QT syndrome and in patients with a history of cardiac arrhythmias. Certain circumstances may increase the risk of the occurrence of torsade de pointes and/or sudden death in association with the use of drugs that prolong the QTc interval, including (1) bradycardia; (2) hypokalemia or hypomagnesemia; (3) concomitant use of other drugs that prolong the QTc interval; and (4) presence of congenital prolongation of the QT interval [see Clinical Pharmacology (12.2) ]. 5.10 Hypotension and Orthostatic Hypotension Tetrabenazine tablet induced postural dizziness in healthy volunteers receiving single doses of 25 or 50 mg. One subject had syncope and one subject with postural dizziness had documented orthostasis. Dizziness occurred in 4% of Tetrabenazine tablet-treated patients (vs. none on placebo) in the 12-week controlled trial; however, blood pressure was not measured during these events. Monitoring of vital signs on standing should be considered in patients who are vulnerable to hypotension. 5.11 Hyperprolactinemia Tetrabenazine tablet elevates serum prolactin concentrations in humans. Following administration of 25 mg to healthy volunteers, peak plasma prolactin levels increased 4- to 5-fold. Tissue culture experiments indicate that approximately one third of human breast cancers are prolactin-dependent in vitro , a factor of potential importance if Tetrabenazine tablet is being considered for a patient with previously detected breast cancer. Although amenorrhea, galactorrhea, gynecomastia and impotence can be caused by elevated serum prolactin concentrations, the clinical significance of elevated serum prolactin concentrations for most patients is unknown. Chronic increase in serum prolactin levels (although not evaluated in the Tetrabenazine tablet development program) has been associated with low levels of estrogen and increased risk of osteoporosis. If there is a clinical suspicion of symptomatic hyperprolactinemia, appropriate laboratory testing should be done and consideration should be given to discontinuation of Tetrabenazine tablet. 5.12 Tardive Dyskinesia (T D) A potentially irreversible syndrome of involuntary, dyskinetic movements may develop in patients treated with neuroleptic drugs. In an animal model of orofacial dyskinesias, acute administration of reserpine, a monoamine depletor, has been shown to produce vacuous chewing in rats. Although the pathophysiology of tardive dyskinesia remains incompletely understood, the most commonly accepted hypothesis of the mechanism is that prolonged post-synaptic dopamine receptor blockade leads to supersensitivity to dopamine. Neither reserpine nor Tetrabenazine tablet, which are dopamine depletors, have been reported to cause clear tardive dyskinesia in humans, but as pre-synaptic dopamine depletion could theoretically lead to supersensitivity to dopamine, and Tetrabenazine tablet can cause the extrapyramidal symptoms also known to be associated with neuroleptics (e.g., parkinsonism and akathisia), physicians should be aware of the possible risk of tardive dyskinesia. If signs and symptoms of TD appear in a patient treated with Tetrabenazine tablet, drug discontinuation should be considered. 5.13 Binding to Melanin-Containing Tissues Since Tetrabenazine tablet or its metabolites bind to melanin-containing tissues, it could accumulate in these tissues over time. This raises the possibility that Tetrabenazine tablet may cause toxicity in these tissues after extended use. Neither ophthalmologic nor microscopic examination of the eye was conducted in the chronic toxicity study in dogs. Ophthalmologic monitoring in humans was inadequate to exclude the possibility of injury occurring after long-term exposure. The clinical relevance of Tetrabenazine tablet's binding to melanin-containing tissues is unknown. Although there are no specific recommendations for periodic ophthalmologic monitoring, prescribers should be aware of the possibility of long-term ophthalmologic effects [see Clinical Pharmacology (12.2) ].