BEPOTASTINE: 87 Adverse Event Reports & Safety Profile
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Active Ingredient: BEPOTASTINE BESYLATE · Drug Class: Histamine-1 Receptor Antagonist [EPC] · Route: OPHTHALMIC · Manufacturer: Bausch & Lomb Incorporated · HUMAN PRESCRIPTION DRUG · FDA Label: Available
First Report: 201306 · Latest Report: 20240522
What Are the Most Common BEPOTASTINE Side Effects?
All BEPOTASTINE Side Effects by Frequency
| Side Effect | Reports | % of Total | Deaths | Hosp. |
|---|---|---|---|---|
| Asthma | 7 | 8.1% | 0 | 2 |
| Off label use | 7 | 8.1% | 0 | 3 |
| Cough | 6 | 6.9% | 0 | 2 |
| Dyspnoea | 6 | 6.9% | 0 | 1 |
| Hepatic function abnormal | 6 | 6.9% | 2 | 3 |
| Nausea | 6 | 6.9% | 0 | 6 |
| Therapeutic product effect incomplete | 6 | 6.9% | 0 | 2 |
| Chronic sinusitis | 5 | 5.8% | 0 | 1 |
| Dyspnoea at rest | 5 | 5.8% | 0 | 1 |
| Dyspnoea exertional | 5 | 5.8% | 0 | 1 |
| Gallbladder disorder | 5 | 5.8% | 0 | 1 |
| Gastrooesophageal reflux disease | 5 | 5.8% | 0 | 1 |
| Hypothyroidism | 5 | 5.8% | 0 | 1 |
| Malaise | 5 | 5.8% | 0 | 5 |
| Obesity | 5 | 5.8% | 0 | 1 |
| Obstructive airways disorder | 5 | 5.8% | 0 | 1 |
| Osteoarthritis | 5 | 5.8% | 0 | 1 |
| Respiratory disorder | 5 | 5.8% | 0 | 1 |
| Wheezing | 5 | 5.8% | 0 | 1 |
Who Reports BEPOTASTINE Side Effects? Age & Gender Data
Gender: 50.0% female, 50.0% male. Average age: 59.6 years. Most reports from: JP. View detailed demographics →
Is BEPOTASTINE Getting Safer? Reports by Year
| Year | Reports | Deaths | Hosp. |
|---|---|---|---|
| 2013 | 2 | 0 | 0 |
| 2014 | 2 | 0 | 1 |
| 2015 | 3 | 0 | 2 |
| 2016 | 10 | 0 | 6 |
| 2017 | 14 | 4 | 9 |
| 2018 | 4 | 0 | 2 |
| 2019 | 5 | 0 | 3 |
| 2020 | 2 | 0 | 0 |
| 2021 | 2 | 0 | 0 |
| 2022 | 6 | 0 | 3 |
| 2023 | 5 | 0 | 2 |
| 2024 | 1 | 0 | 1 |
What Is BEPOTASTINE Used For?
| Indication | Reports |
|---|---|
| Product used for unknown indication | 40 |
| Urticaria | 7 |
Other Drugs in Same Class: Histamine-1 Receptor Antagonist [EPC]
Official FDA Label for BEPOTASTINE
Official prescribing information from the FDA-approved drug label.
Drug Description
Bepotastine Besilate Ophthalmic Solution, 1.5% is a sterile, topically administered drug for ophthalmic use. Each mL of Bepotastine Besilate Ophthalmic Solution contains 15 mg bepotastine besilate. Bepotastine besilate is designated chemically as (+) -4-[[(S)-p-chloro-alpha -2-pyridylbenzyl]oxy]-1-piperidine butyric acid monobenzenesulfonate. The chemical structure for bepotastine besilate is: Bepotastine besilate is a white to pale yellowish-white crystalline powder. The molecular weight of bepotastine besilate is 547.06 daltons.
Bepotastine Besilate Ophthalmic
Solution is supplied as a sterile, aqueous 1.5% solution, with an approximate pH of 6.8. The osmolality of Bepotastine Besilate Ophthalmic Solution, 1.5% is approximately 295 mOsm/kg. Each mL of Bepotastine Besilate Ophthalmic Solution, 1.5% contains: Active: bepotastine besilate 15 mg (equivalent to 10.7 mg bepotastine) Inactives: monobasic sodium phosphate dihydrate, sodium chloride, sodium hydroxide to adjust pH, and water for injection, USP Preservative: benzalkonium chloride 0.005% Chemical Structure
FDA Approved Uses (Indications)
AND USAGE Bepotastine Besilate Ophthalmic Solution, 1.5% is a histamine H 1 receptor antagonist indicated for the treatment of itching associated with signs and symptoms of allergic conjunctivitis.
Bepotastine Besilate Ophthalmic
Solution is a histamine H1 receptor antagonist indicated for the treatment of itching associated with allergic conjunctivitis. ( 1 )
Dosage & Administration
AND ADMINISTRATION Instill one drop of Bepotastine Besilate Ophthalmic Solution into the affected eye(s) twice a day. Remove contact lenses prior to instillation of Bepotastine Besilate Ophthalmic Solution. Instill one drop into the affected eye(s) twice a day. ( 2 ) Remove contact lenses prior to instillation of Bepotastine Besilate Ophthalmic Solution. ( 2 )
Contraindications
Bepotastine Besilate Ophthalmic Solution is contraindicated in patients with a history of hypersensitivity reactions to bepotastine or any of the other ingredients [see Adverse Reactions (6.2) ] . Hypersensitivity to any component of this product. ( 4 )
Known Adverse Reactions
REACTIONS The most common adverse reaction occurring in approximately 25% of patients was a mild taste following instillation. Other adverse reactions which occurred in 2-5% of subjects were eye irritation, headache, and nasopharyngitis. ( 6.1 ) To report SUSPECTED ADVERSE REACTIONS, contact Bausch & Lomb Incorporated at 1-800-553-5340 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
6.1 Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in clinical practice. The most common reported adverse reaction occurring in approximately 25% of subjects was a mild taste following instillation. Other adverse reactions occurring in 2-5% of subjects were eye irritation, headache, and nasopharyngitis.
6.2 Post-Marketing Experience Hypersensitivity reactions have been reported rarely during the post-marketing use of Bepotastine Besilate Ophthalmic Solution. Because these reactions are reported voluntarily from a population of unknown size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure. The hypersensitivity reactions may include itching, body rash, and swelling of lips, tongue and/or throat.
6.1 Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in clinical practice. The most common reported adverse reaction occurring in approximately 25% of subjects was a mild taste following instillation. Other adverse reactions occurring in 2-5% of subjects were eye irritation, headache, and nasopharyngitis.
6.2 Post-Marketing Experience Hypersensitivity reactions have been reported rarely during the post-marketing use of Bepotastine Besilate Ophthalmic Solution. Because these reactions are reported voluntarily from a population of unknown size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure. The hypersensitivity reactions may include itching, body rash, and swelling of lips, tongue and/or throat.
Warnings
AND PRECAUTIONS Contamination of Solution: Do not touch the dropper tip to any surface. Keep bottle tightly closed when not in use. ( 5.1 )
Contact Lens
Wear: Bepotastine Besilate Ophthalmic Solution should not be used to treat contact lens-related irritation. ( 5.2 )
5.1 Contamination of Tip and Solution To minimize contaminating the dropper tip and solution, advise the patient not to touch the eyelids or surrounding areas with the dropper tip of the bottle and to keep the bottle tightly closed when not in use.
5.2 Contact Lens Wear Bepotastine Besilate Ophthalmic Solution should not be used to treat contact lens-related irritation.
Bepotastine Besilate Ophthalmic
Solution should not be instilled while wearing contact lenses. Patient should remove contact lenses prior to instillation of Bepotastine Besilate Ophthalmic Solution, because benzalkonium chloride may be absorbed by soft contact lenses. Lenses may be reinserted after 10 minutes following administration of Bepotastine Besilate Ophthalmic Solution.
5.1 Contamination of Tip and Solution To minimize contaminating the dropper tip and solution, advise the patient not to touch the eyelids or surrounding areas with the dropper tip of the bottle and to keep the bottle tightly closed when not in use.
5.2 Contact Lens Wear Bepotastine Besilate Ophthalmic Solution should not be used to treat contact lens-related irritation.
Bepotastine Besilate Ophthalmic
Solution should not be instilled while wearing contact lenses. Patient should remove contact lenses prior to instillation of Bepotastine Besilate Ophthalmic Solution, because benzalkonium chloride may be absorbed by soft contact lenses. Lenses may be reinserted after 10 minutes following administration of Bepotastine Besilate Ophthalmic Solution.