|
| Generic
Available |
|
|
No |

|
|
| Synonyms |
|
|
Biphenabid |

|
|
| Pharmacological Index |
|
|
Antilipemic Agent (Miscellaneous) |

|
|
| Use |
|
|
Adjunct to dietary therapy to decrease elevated serum total and LDL
cholesterol concentrations in primary hypercholesterolemia |

|
|
| Pregnancy Risk
Factor |
|
|
B |

|
|
| Contraindications |
|
|
Ventricular arrhythmias; hypersensitivity to probucol or any
component |

|
|
| Adverse
Reactions |
|
|
>10%:
Cardiovascular: Q-T prolongation, serious arrhythmias
Gastrointestinal: Bloating, diarrhea, stomach pain, nausea, vomiting
1% to 10%: Central nervous system: Dizziness, headache, numbness of
extremities |

|
|
| Drug
Interactions |
|
|
Increased toxicity: Drugs that prolong the Q-T interval (eg, tricyclic
antidepressants, some antiarrhythmic agents, phenothiazines) or with drugs that
affect the atrial rate (eg, beta-adrenergic blocking agents) or that can cause
A-V block (eg, digoxin) |

|
|
| Mechanism of
Action |
|
|
Increases the fecal loss of bile acid-bound low density lipoprotein
cholesterol, decreases the synthesis of cholesterol and inhibits enteral
cholesterol absorption |

|
|
| Usual Dosage |
|
|
Oral:
<27 kg: 250 mg twice daily with meals
>27 kg: 500 mg twice daily with meals
Adults: 500 mg twice daily administered with the morning and evening meals
|

|
|
| Mental Health: Effects
on Mental Status |
|
|
May cause dizziness |

|
|
| Mental Health:
Effects on Psychiatric
Treatment |
|
|
Concurrent use with phenothiazines, TCAs, or beta-blockers may produce AV
block |

|
|
| Dental Health: Local
Anesthetic/Vasoconstrictor
Precautions |
|
|
No information available to require special precautions |

|
|
| Dental Health:
Effects on Dental Treatment |
|
|
No effects or complications reported |

|
|
| Patient
Information |
|
|
Take with meals; notify physician if diarrhea, abdominal pain, nausea, or
vomiting becomes severe or persist |

|
|
| Dosage Forms |
|
|
Tablet: 250 mg, 500 mg |

|
|
Copyright © 2007 Drugs Area
|