Unoprostone
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1];
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Overview
Unoprostone is a {{{drugClass}}} that is FDA approved for the treatment of open-angle glaucoma or ocular hypertension. Common adverse reactions include burning/stinging, burning/stinging upon drug instillation, dry eyes, itching, increased length of eyelashes and injection.
Adult Indications and Dosage
FDA-Labeled Indications and Dosage (Adult)
Open-Angle Glaucoma=
- Rescula (unoprostone isopropyl ophthalmic solution) 0.15% is indicated for the lowering of intraocular pressure in patients with open-angle glaucoma or ocular hypertension.
- The recommended dosage is one drop in the affected eye(s) twice daily.
- Rescula may be used concomitantly with other topical ophthalmic drug products to lower intraocular pressure. If two drugs are used, they should be administered at least five (5) minutes apart.
Off-Label Use and Dosage (Adult)
Guideline-Supported Use
Condition1
- Developed by:
- Class of Recommendation:
- Strength of Evidence:
- Dosing Information
- Dosage
Condition2
There is limited information regarding Off-Label Guideline-Supported Use of Unoprostone in adult patients.
Non–Guideline-Supported Use
Condition1
- Dosing Information
- Dosage
Condition2
There is limited information regarding Off-Label Non–Guideline-Supported Use of Unoprostone in adult patients.
Pediatric Indications and Dosage
FDA-Labeled Indications and Dosage (Pediatric)
Condition1
- Dosing Information
- Dosage
Condition2
There is limited information regarding FDA-Labeled Use of Unoprostone in pediatric patients.
Off-Label Use and Dosage (Pediatric)
Guideline-Supported Use
Condition1
- Developed by:
- Class of Recommendation:
- Strength of Evidence:
- Dosing Information
- Dosage
Condition2
There is limited information regarding Off-Label Guideline-Supported Use of Unoprostone in pediatric patients.
Non–Guideline-Supported Use
Condition1
- Dosing Information
- Dosage
Condition2
There is limited information regarding Off-Label Non–Guideline-Supported Use of Unoprostone in pediatric patients.
Contraindications
- Rescula is contraindicated in patients with hypersensitivity to unoprostone isopropyl or any other ingredient in this product.
Warnings
- Description
Precautions
- Description
Adverse Reactions
Clinical Trials Experience
There is limited information regarding Clinical Trial Experience of Unoprostone in the drug label.
Body as a Whole
Cardiovascular
Digestive
Endocrine
Hematologic and Lymphatic
Metabolic and Nutritional
Musculoskeletal
Neurologic
Respiratory
Skin and Hypersensitivy Reactions
Special Senses
Urogenital
Miscellaneous
Postmarketing Experience
There is limited information regarding Postmarketing Experience of Unoprostone in the drug label.
Body as a Whole
Cardiovascular
Digestive
Endocrine
Hematologic and Lymphatic
Metabolic and Nutritional
Musculoskeletal
Neurologic
Respiratory
Skin and Hypersensitivy Reactions
Special Senses
Urogenital
Miscellaneous
Drug Interactions
- Drug
- Description
Use in Specific Populations
Pregnancy
- Pregnancy Category
- Australian Drug Evaluation Committee (ADEC) Pregnancy Category
There is no Australian Drug Evaluation Committee (ADEC) guidance on usage of Unoprostone in women who are pregnant.
Labor and Delivery
There is no FDA guidance on use of Unoprostone during labor and delivery.
Nursing Mothers
There is no FDA guidance on the use of Unoprostone with respect to nursing mothers.
Pediatric Use
There is no FDA guidance on the use of Unoprostone with respect to pediatric patients.
Geriatic Use
There is no FDA guidance on the use of Unoprostone with respect to geriatric patients.
Gender
There is no FDA guidance on the use of Unoprostone with respect to specific gender populations.
Race
There is no FDA guidance on the use of Unoprostone with respect to specific racial populations.
Renal Impairment
There is no FDA guidance on the use of Unoprostone in patients with renal impairment.
Hepatic Impairment
There is no FDA guidance on the use of Unoprostone in patients with hepatic impairment.
Females of Reproductive Potential and Males
There is no FDA guidance on the use of Unoprostone in women of reproductive potentials and males.
Immunocompromised Patients
There is no FDA guidance one the use of Unoprostone in patients who are immunocompromised.
Administration and Monitoring
Administration
- Oral
- Intravenous
Monitoring
There is limited information regarding Monitoring of Unoprostone in the drug label.
- Description
IV Compatibility
There is limited information regarding IV Compatibility of Unoprostone in the drug label.
Overdosage
Acute Overdose
Signs and Symptoms
- Description
Management
- Description
Chronic Overdose
There is limited information regarding Chronic Overdose of Unoprostone in the drug label.
Pharmacology
There is limited information regarding Unoprostone Pharmacology in the drug label.
Mechanism of Action
Structure
Pharmacodynamics
There is limited information regarding Pharmacodynamics of Unoprostone in the drug label.
Pharmacokinetics
There is limited information regarding Pharmacokinetics of Unoprostone in the drug label.
Nonclinical Toxicology
There is limited information regarding Nonclinical Toxicology of Unoprostone in the drug label.
Clinical Studies
There is limited information regarding Clinical Studies of Unoprostone in the drug label.
How Supplied
Storage
There is limited information regarding Unoprostone Storage in the drug label.
Images
Drug Images
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Package and Label Display Panel
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Patient Counseling Information
There is limited information regarding Patient Counseling Information of Unoprostone in the drug label.
Precautions with Alcohol
- Alcohol-Unoprostone interaction has not been established. Talk to your doctor about the effects of taking alcohol with this medication.
Brand Names
- ®[1]
Look-Alike Drug Names
- A® — B®[2]
Drug Shortage Status
Price
References
The contents of this FDA label are provided by the National Library of Medicine.
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- ↑ "http://www.ismp.org". External link in
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