Ocu-Tropic Side Effects
Generic name: tropicamide ophthalmic
Medically reviewed by Drugs.com. Last updated on Feb 20, 2024.
Note: This document provides detailed information about Ocu-Tropic Side Effects associated with tropicamide ophthalmic. Some dosage forms listed on this page may not apply specifically to the brand name Ocu-Tropic.
Applies to tropicamide ophthalmic: ophthalmic solution.
Common side effects of Ocu-Tropic
Some side effects of tropicamide ophthalmic may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects.
Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:
More common
- blurred vision
- headache
- sensitivity of eyes to light
- stinging of the eye when the medicine is applied
Serious side effects of Ocu-Tropic
Along with its needed effects, tropicamide ophthalmic (the active ingredient contained in Ocu-Tropic) may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.
Check with your doctor as soon as possible if any of the following side effects occur while taking tropicamide ophthalmic:
Symptoms of too much medicine being absorbed into the body
- Clumsiness or unsteadiness
- confusion
- fast heartbeat
- flushing or redness of face
- hallucinations (seeing, hearing, or feeling things that are not there)
- increased thirst or dryness of mouth
- skin rash
- slurred speech
- swollen stomach in infants
- unusual behavior, especially in children
- unusual drowsiness, tiredness, or weakness
For Healthcare Professionals
Applies to tropicamide ophthalmic: compounding powder, ophthalmic solution.
General
Side effects reported with this drug have included transient stinging, blurred vision, photophobia and superficial punctate keratitis. Some patients have experienced prolonged mydriasis.[Ref]
Ocular
- Frequency not reported: Headache, drowsiness, somnolence, fatigue, trouble concentrating, central nervous system disturbances, dysphonia
- Postmarketing reports: Dizziness[Ref]
Psychiatric
- Frequency not reported: Psychotic reaction, behavioral disturbance[Ref]
Behavioral disturbances or psychotic reactions may be more common in children.[Ref]
Nervous system
- Frequency not reported: Headache, drowsiness, somnolence, fatigue, trouble concentrating, central nervous system disturbances, dysphonia
- Postmarketing reports: Dizziness[Ref]
Cardiovascular
- Frequency not reported: Tachycardia, bradycardia, arrhythmias, palpitations
- Postmarketing reports: Hypotension, syncope[Ref]
Transient bradycardia followed by tachycardia with palpitations and arrhythmias have been reported.[Ref]
Hypersensitivity
- Frequency not reported: Allergic reaction, anaphylaxis[Ref]
Gastrointestinal
Respiratory
- Frequency not reported: Rhinitis, reduced bronchial secretions, bronchospasm
- Postmarketing reports: Dryness of mucous membranes[Ref]
Genitourinary
- Frequency not reported: Urinary retention, difficult micturition[Ref]
Dermatologic
- Frequency not reported: Erythematous rash, pruritus, pallor, flushing, increased sweating, dry skin[Ref]
Musculoskeletal
- Frequency not reported: Muscle rigidity[Ref]
References
1. Cerner Multum, Inc. "UK Summary of Product Characteristics."
2. Cerner Multum, Inc. "Australian Product Information."
3. (2016) "Product Information. Tropicamide (tropicamide ophthalmic)." Bausch and Lomb Americas, Inc.
More about Ocu-Tropic (tropicamide ophthalmic)
- Check interactions
- Compare alternatives
- Dosage information
- During pregnancy
- Drug class: mydriatics
- Breastfeeding
Patient resources
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Further information
Ocu-Tropic side effects can vary depending on the individual. Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
Some side effects may not be reported. You may report them to the FDA.