|
| Pronunciation |
|
(bye
PER i
den) |

|
|
| U.S. Brand
Names |
|
| Akineton® |

|
|
| Generic
Available |
|
|
No |

|
|
| Synonyms |
|
|
Biperiden Hydrochloride; Biperiden Lactate |

|
|
| Pharmacological Index |
|
|
Anticholinergic Agent; Anti-Parkinson's Agent
(Anticholinergic) |

|
|
| Use |
|
|
Adjunct in the therapy of all forms of Parkinsonism; control of
extrapyramidal symptoms secondary to antipsychotics |

|
|
| Pregnancy Risk
Factor |
|
|
C |

|
|
| Contraindications |
|
|
Angle-closure glaucoma; GI or GU obstruction; hypersensitivity to
biperiden |

|
|
| Warnings/Precautions |
|
|
Use with caution in patients with angle-closure glaucoma, peptic ulcer,
urinary tract obstruction, hyperthyroidism; some preparations contain sodium
bisulfite; syrup contains alcohol |

|
|
| Adverse
Reactions |
|
|
Cardiovascular: Orthostatic hypotension, bradycardia (I.V.)
Central nervous system: Drowsiness, euphoria, disorientation, agitation
Gastrointestinal: Constipation, xerostomia
Genitourinary: Urinary retention
Ocular: Blurred vision |

|
|
| Drug
Interactions |
|
|
Decreased effect: May increase gastric degradation of levodopa and decrease
the amount of levodopa absorbed by delaying gastric emptying; the opposite may
be true for digoxin
Therapeutic effects of cholinergic agents (tacrine, donepezil) and
neuroleptics may be antagonized
Increased toxicity: Central and/or peripheral anticholinergic syndrome can
occur when administered with amantadine, rimantadine, narcotic analgesics,
phenothiazines and other antipsychotics (especially with high anticholinergic
activity), tricyclic antidepressants, quinidine and some other antiarrhythmics,
and antihistamines |

|
|
| Mechanism of
Action |
|
|
Biperiden is a weak peripheral anticholinergic agent with nicotinolytic
activity. The beneficial effects in Parkinson's disease and neuroleptic-induced
extrapyramidal reactions are believed to be due to the inhibition of striatal
cholinergic receptors. |

|
|
| Pharmacodynamics/Kinetics |
|
|
Serum half-life: 18.4-24.3 hours
Time to peak serum concentration: 1-1.5 hours |

|
|
| Usual Dosage |
|
|
Adults:
Extrapyramidal:
Oral: 2 mg 1-3 times/day
I.M., I.V.: 2 mg every 30 minutes up to 4 doses or 8 mg/day
|

|
|
| Administration |
|
|
I.V. must be given slowly |

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

|
|
| Dental Health:
Effects on Dental Treatment |
|
|
Dry mouth, nose, and throat very prevalent in patients taking this
drug |

|
|
| Patient
Information |
|
|
May cause drowsiness |

|
|
| Nursing
Implications |
|
|
No significant difference in onset of I.M. or I.V. injection, therefore,
there is usually no need to use the I.V. route. Improvement is sometimes
noticeable a few minutes after injection. Do not discontinue drug
abruptly. |

|
|
| Dosage Forms |
|
|
Injection, as lactate: 5 mg/mL (1 mL)
Tablet, as hydrochloride: 2 mg
|

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