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DEUTETRABENAZINE


DIR Classification


Classification:Most-DIR concern
Severity Score:4

Description in Drug Labeling: View Full Labeling: SPL in DailyMed | PDF

  • WARNINGS AND PRECAUTIONS
  • QTc Prolongation
  • AUSTEDO may prolong the QT interval, but the degree of QT prolongation is not clinically significant when AUSTEDO is administered within the recommended dosage range [see Clinical Pharmacology (12.2)].
  • AUSTEDO should 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.
  • ADVERSE REACTIONS
  • The following serious adverse reactions are discussed in greater detail in other sections of the labeling:
  • Depression and Suicidality in Patients with Huntington’s disease [see Warnings and Precautions (5.1)]
  • QTc Prolongation [see Warnings and Precautions (5.3)]
  • Neuroleptic Malignant Syndrome (NMS) [see Warnings and Precautions (5.4)]
  • Akathisia, Agitation, and Restlessness [see Warnings and Precautions (5.5)]
  • Parkinsonism [see Warnings and Precautions (5.6)]
  • Sedation and Somnolence [see Warnings and Precautions (5.7)]
  • Hyperprolactinemia [see Warnings and Precautions (5.8)]
  • Binding to Melanin-Containing Tissues [see Warnings and Precautions (5.9)]
  • CLINICAL PHARMACOLOGY
  • Pharmacodynamics
  • Cardiac Electrophysiology
  • At the maximum recommended dose, AUSTEDO does not prolong the QT interval to any clinically relevant extent. An exposure-response analysis on QTc prolongation from a study in extensive or intermediate (EM) and poor CYP2D6 metabolizers (PM) showed that a clinically-relevant effect can be excluded at exposures following single doses of 24 and 48 mg of AUSTEDO.
  • PATIENT COUNSELING INFORMATION
  • Prolongation of the QTc Interval
  • Inform patients to consult their physician immediately if they feel faint, lose consciousness, or have heart palpitations [see Warnings and Precautions (5.3)]. Advise patients to inform physicians that they are taking AUSTEDO before any new drug is taken.
  • MEDICATION GUIDE
  • Before taking AUSTEDO, tell your healthcare provider about all of your medical conditions, including if you:
  • have emotional or mental problems (for example, depression, nervousness, anxiety, anger, agitation, psychosis, previous suicidal thoughts or suicide attempts).
  • have liver disease.
  • have an irregular heart rhythm or heartbeat (QT prolongation, cardiac arrhythmia) or a heart problem called congenital long QT syndrome.
  • have low levels of potassium or magnesium in your blood (hypokalemia or hypomagnesemia).
  • have breast cancer or a history of breast cancer.
  • are pregnant or plan to become pregnant. It is not known if AUSTEDO can harm your unborn baby.
  • are breastfeeding or plan to breastfeed. It is not known if AUSTEDO passes into breast milk.
  • AUSTEDO can cause serious side effects, including:
  • Irregular heartbeat (QT prolongation). AUSTEDO increases your chance of having certain changes in the electrical activity in your heart. These changes can lead to a dangerous abnormal heartbeat. Taking AUSTEDO with certain medicines may increase this chance.

Postmarketing Surveillance

Contingency Table:

Current Drug
Other Drugs
Rhabdomyolysis
0
42912
Other ADRs
4
14117275

Odds Ratio = N/A

Drug Property Information



ATC Code(s): N/A
Active Ingredient:deutetrabenazine
Active Ingredient UNII:P341G6W9NB
Drugbank ID:DB12161
PubChem Compound:73442840
CAS Number:1392826-25-3
Dosage Form(s):tablet, coated
Route(s) Of Administrator:oral
Daily Dose:
Chemical Structure:
SMILE Code:
[2H]C([2H])([2H])OC1=C(C=C2[C@@H]3CC(=O)[C@H](CN3CCC2=C1)CC(C)C)OC([2H])([2H])[2H]

Reference

COHORT STUDY:

N/A

OTHER REFERENCE(S):

N/A

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