Bemote Side Effects

Generic name: dicyclomine

Medically reviewed by Drugs.com. Last updated on Jun 21, 2024.

Note: This document provides detailed information about Bemote.

Applies to dicyclomine: oral capsules and tablets, oral solution, parenteral injection Side Effects associated with dicyclomine. Some dosage forms listed on this page may not apply specifically to the brand name Bemote.

Applies to dicyclomine: oral capsules and tablets, oral solution, parenteral injection.

Side effects include:

Most adverse effects are manifestations of pharmacologic effects at muscarinic-cholinergic receptors and usually are reversible when therapy is discontinued.

Severity and frequency of adverse effects are dose related and individual intolerance varies greatly; although adverse effects occasionally may be obviated by a reduction in dosage, this also will likely eliminate potential therapeutic effects. If dosage of ≥80 mg daily cannnot be achieved because of intolerance, discontinue dicyclomine (the active ingredient contained in Bemote)

Dry mouth, dizziness, blurred vision, nausea, light-headedness (especially with the injectable form), drowsiness, weakness, nervousness.

For healthcare professionals

Applies to dicyclomine: compounding powder, intramuscular solution, oral capsule, oral syrup, oral tablet.

General

The most serious adverse reactions include cardiovascular and central nervous system symptoms.

The most common adverse reactions are dizziness, dry mouth, vision blurred, nausea, somnolence, asthenia and nervousness, fever, tachycardia, agitation, and dry skin/mucous membranes.^[Ref]

Gastrointestinal

• Very common (10% or more): Dry mouth (33%), nausea (14%)
• Rare (less than 0.1%): Constipation, anorexia
• Frequency not reported: Thirst, delayed gastric emptying time, reduced gastric acid secretion, gastroesophageal reflux
• Postmarketing reports: Abdominal distension, abdominal pain, dyspepsia, constipation, dry mouth, nausea, vomiting^[Ref]

Nervous system

• Very common (10% or more): Dizziness (40%)
• Common (1% to 10%): Somnolence, nervousness
• Rare (less than 0.1%): Sedation, headache
• Postmarketing reports: Dizziness, headache, somnolence, syncope^[Ref]

Ocular

• Very common (10% or more): Blurred vision (27%)
• Frequency not reported: Follicular conjunctivitis, all muscarinic antagonists can precipitate glaucoma
• Postmarketing reports: Cycloplegia, mydriasis, blurred vision^[Ref]

Other

• Common (1% to 10%): Asthenia
• Frequency not reported: Fatigue
• Postmarketing reports: Malaise, fatigue^[Ref]

Dermatologic

• Rare (less than 0.1%): Rash
• Postmarketing reports: Allergic dermatitis, erythema, rash^[Ref]

Renal

• Rare (less than 0.1%): Dysuria^[Ref]

Genitourinary

• Frequency not reported: Urinary retention, impotence in male patients
• Postmarketing reports: Suppressed lactation^[Ref]

Cardiovascular

• Postmarketing reports: Palpitations, tachyarrhythmias, thrombosis, thrombophlebitis^[Ref]

Hypersensitivity

• Postmarketing reports: Face edema, angioedema, anaphylactic shock^[Ref]

Local

• Postmarketing reports: Local pain, edema, skin color change, reflex sympathetic dystrophy syndrome (caused by inadvertent IV injection)^[Ref]

Psychiatric

• Postmarketing reports: Delirium or symptoms of delirium such as amnesia (or transient global amnesia), nervousness, agitation, confusional state, delusion, disorientation, hallucination (including visual hallucination), and mania, mood (altered and pseudodementia).^[Ref]

Respiratory

• Postmarketing reports: Dyspnea, nasal congestion^[Ref]

Further information

Bemote 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.

Medical Disclaimer