Cyclopentolate Other names: Cyclopentolate hydrochloride

Chemical formula: C₁₇H₂₅NO₃  Molecular mass: 291.385 g/mol  PubChem compound: 2905

Interactions

Cyclopentolate interacts in the following cases:

Anti-muscarinic agents

The effects of anti-muscarinic agents may be enhanced by the concomitant administration of other drugs with antimuscarinic properties such as some antihistamines, butyrophenones, phenothiazines, tricyclic antidepressants and amantadine.

Previous serious systemic adverse reaction to atropine

at least one of
Atropine allergy
Atropine adverse reaction

Children with epilepsy

Cyclopentolate should be used with caution in children with known epilepsy.

Pregnancy

There is insufficient evidence as to drug safety in pregnancy. This product should not be used during pregnancy unless it is considered essential by a physician.

Nursing mothers

There is insufficient evidence as to drug safety in lactation.

Effects on ability to drive and use machines

May cause blurred vision, difficulty in focusing and sensitivity to light. Patients should be warned not to drive or engage in other hazardous activities (including climbing ladders and scaffolding) unless vision is clear. Complete recovery from the effects of cyclopentolate eye drops may take up to 24 hours.

Adverse reactions


Frequencies are defined according to the following convention: very common (≥1/100), common ≥1/100 to 1/10, uncommon ≥1/1,000 to <1/100, rare (≥11/10,000 to <1,000), very rare (<1/10,000), not known (cannot be estimated from the available data).

System organ classAdverse reactionsFrequency
Psychiatric disorders abnormal behavioura, psychotic disordersa not known
Nervous system disorders dizziness, convulsionsb, partial seizuresb not known
Eye disorders eye pain, increased intraocular pressure, eye
oedema1, eye irritation (stinging)1, ocular
hyperaemia1, conjunctivitis1, photophobia2
not known
Cardiac disorders bradycardia, tachycardia, palpitations, arrhythmia,
cardiopulmonary failurea
not known
Vascular disorders flushingnot known
Gastrointestinal disorders dry mouth, vomiting, gastrointestinal hypomotility and
constipation, abdominal distensionc, necrotising
enterocolitisd
not known
Skin and subcutaneous disorders dry skin, skin rasha not known
Renal and urinary disorders urinary urgency, urinary retention, dysurianot known
General disorders and administration site conditions gait disturbancenot known

Notes:

General

1 Following prolonged administration
2 Secondary to pupillary dilation

Paediatric population

a Abnormal behaviour, psychotic disorders, cardiopulmonary failure and skin rashes have been reported in the paediatric population.
b Convulsions and partial seizures have been reported in children, although the cases reported to date have been low in number or isolated.
c Cases of abdominal distension have been reported in infants.
d Necrotising enterocolitis has been reported in preterm infants.

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