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| U.S. Brand
Names |
|
| Mydriacyl®; Opticyl®;
Tropicacyl® |

|
|
| Generic
Available |
|
|
Yes |

|
|
| Synonyms |
|
|
Bistropamide |

|
|
| Pharmacological Index |
|
|
Ophthalmic Agent, Mydriatic |

|
|
| Use |
|
|
Short-acting mydriatic used in diagnostic procedures; as well as
preoperatively and postoperatively; treatment of some cases of acute iritis,
iridocyclitis, and keratitis |

|
|
| Pregnancy Risk
Factor |
|
|
C |

|
|
| Contraindications |
|
|
Glaucoma, hypersensitivity to tropicamide or any
component |

|
|
| Warnings/Precautions |
|
|
Use with caution in infants and children since tropicamide may cause
potentially dangerous CNS disturbances; tropicamide may cause an increase in
intraocular pressure |

|
|
| Adverse
Reactions |
|
|
1% to 10%:
Central nervous system: Parasympathetic stimulations, drowsiness, headache
Dermatologic: Eczematoid dermatitis
Gastrointestinal: Xerostomia
Local: Transient stinging
Ocular: Blurred vision, photophobia with or without corneal staining,
increased intraocular pressure, follicular conjunctivitis |

|
|
| Overdosage/Toxicology |
|
|
Symptoms of overdose include blurred vision, urinary retention, tachycardia,
cardiorespiratory collapse
Antidote is physostigmine, pilocarpine; anticholinergic toxicity is caused by
strong binding of the drug to cholinergic receptors. For anticholinergic
overdose with severe life-threatening symptoms, physostigmine 1-2 mg (0.5 mg or
0.02 mg/kg for children) S.C. or I.V., slowly may be given to reverse systemic
effects. |

|
|
| Stability |
|
|
Store in tightly closed containers |

|
|
| Mechanism of
Action |
|
|
Prevents the sphincter muscle of the iris and the muscle of the ciliary body
from responding to cholinergic stimulation |

|
|
| Pharmacodynamics/Kinetics |
|
|
Onset of mydriasis: ~20-40 minutes Duration: ~6-7 hours;
Onset of cycloplegia: Within 30 minutes; Duration: <6 hours
|

|
|
| Usual Dosage |
|
|
Children and Adults (individuals with heavily pigmented eyes may require
larger doses):
Exam must be performed within 30 minutes after the repeat dose; if the
patient is not examined within 20-30 minutes, instill an additional drop
Mydriasis: Instill 1-2 drops (0.5%) 15-20 minutes before exam; may repeat
every 30 minutes as needed |

|
|
| Monitoring
Parameters |
|
|
Ophthalmic exam |

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

|
|
| Mental Health:
Effects on Psychiatric
Treatment |
|
|
None reported |

|
|
| 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 |
|
|
If irritation persists or increases, discontinue use, may cause blurred
vision and increased light sensitivity |

|
|
| Nursing
Implications |
|
|
Finger pressure should be applied on the lacrimal sac for 1-2 minutes
following topical instillation of the solution |

|
|
| Dosage Forms |
|
|
Solution, ophthalmic: 0.5% (2 mL, 15 mL); 1% (2 mL, 3 mL, 15
mL) |

|
|
| References |
|
|
Caputo AR and Schnitzer RE,
"Systemic Response to Mydriatic Eyedrops in Neonates: Mydriatics in Neonates,"
J Pediatr Ophthalmol Strabismus, 1978, 15(2):109-22.
|

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Copyright © 2007 Drugs Area
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