Verelan Side Effects

Generic name: verapamil

Medically reviewed by Drugs.com. Last updated on May 27, 2024.

Note: This document provides detailed information about Verelan Side Effects associated with verapamil. Some dosage forms listed on this page may not apply specifically to the brand name Verelan.

Applies to verapamil: oral capsule extended release, oral tablet, oral tablet extended release.

Other dosage forms:

• intravenous solution

Precautions

It is very important that your doctor check your progress at regular visits to make sure this medicine is working properly and to check for unwanted effects .

Low blood pressure (hypotension) may occur while taking this medicine. Check with your doctor right away if you have the following symptoms: blurred vision; confusion; severe dizziness, faintness, or lightheadedness when getting up from a lying or sitting position suddenly; sweating; or unusual tiredness or weakness .

While you are taking this medicine be careful to limit the amount of alcohol that you drink. Alcohol increases dizziness and drowsiness and also lowers blood pressure .

Common side effects of Verelan

Some side effects of verapamil 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:

Serious side effects of Verelan

Along with its needed effects, verapamil (the active ingredient contained in Verelan) 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 immediately if any of the following side effects occur while taking verapamil:

For healthcare professionals

Applies to verapamil: compounding powder, intravenous solution, oral capsule extended release, oral tablet, oral tablet extended release.

General adverse events

The most commonly reported side effects include constipation, dizziness, and headache.^[Ref]

Nervous system

• Very common (10% or more): Headache (up to 12.1%)
• Common (1% to 10%): Dizziness, lethargy
• Rare (0.01% to 0.1%): Seizures
• Frequency not reported: Rotary nystagmus, sleepiness, vertigo, lightheadedness, tingling, numbness, neuropathy
• Postmarketing reports: Syncope, cerebrovascular accident, equilibrium disorders, parkinsonism/extrapyramidal symptoms/syndrome, paresthesia, shakiness/tremor, paralysis/tetraparesis, somnolence^[Ref]

Seizures occurred rarely with IV administration.

Paralysis/tetraparesis was reported in a patient taking this drug and colchicine concurrently.^[Ref]

Cardiovascular

• Common (1% to 10%): Symptomatic hypotension/hypotension/abrupt blood pressure fall, sinus bradycardia/bradycardia (heart rate less than 50 beats/minute), severe tachycardia, ankle edema/edema, development/aggravation of congestive heart failure (CHF), atrioventricular (AV) block, peripheral edema
• Uncommon (0.1% to 1%): Second-/third-degree AV block, palpitations, orthostasis
• Postmarketing reports: Angina pectoris/chest pain, AV dissociation, ECG abnormal, claudication, hypertension, myocardial infarction, sinus arrest with asystole, decreased myocardial contractility, cardiogenic shock, bradyarrhythmia in atrial fibrillation, vasculitis, erythromelalgia^[Ref]

Cardiovascular side effects may occur with greater intensity at higher doses or in patients with a history of myocardial damage.

Approximately 15% of patients who had atrial flutter/fibrillation and received this drug and digoxin developed resting ventricular rates below 50 beats/min; in the same trial, asymptomatic hypotension occurred in approximately 5% of patients.

Asystole occurred after second/third degree AV block and was usually short in duration, with spontaneous cardiac action returning within seconds in the form of a sinus rhythm.^[Ref]

Gastrointestinal

• Common (1% to 10%): Constipation, dyspepsia, nausea, diarrhea, flatulence
• Uncommon (0.1% to 1%): Abdominal discomfort/pain
• Frequency not reported: Non-obstructive paralytic ileus/ileus, bloating
• Postmarketing reports: Dry mouth, gastrointestinal stress, gingival hyperplasia, vomiting^[Ref]

Non-obstructive paralytic ileus was reversible when treatment was stopped.

Gingival hyperplasia occurred when this drug was given over a prolonged period of time, and was reversible once the drug was discontinued.^[Ref]

Respiratory

• Common (1% to 10%): Pulmonary edema, pharyngitis, sinusitis, rhinitis, dyspnea
• Rare (0.01% to 0.1%): Broncho/laryngeal spasm^[Ref]

Bronchospasm and laryngeal spasm occurred during hypersensitivity reactions.^[Ref]

Other

• Common (1% to 10%): Fatigue, tiredness/malaise, accidental injury, pain
• Frequency not reported: Infection, flu syndrome
• Postmarketing reports: Tinnitus, asthenia^[Ref]

Dermatologic

• Common (1% to 10%): Scalp irritation, rash
• Uncommon (0.1% to 1%): Itching, urticaria, flushing, exanthema
• Frequency not reported: Diaphoresis, photodermatitis
• Postmarketing reports: Ecchymosis, bruising, alopecia/hair loss, hyperkeratosis, macules, Stevens-Johnson syndrome, hyperhidrosis/sweating, erythema multiforme, Quincke's edema/angioneurotic edema^[Ref]

Itch and urticaria occurred in hypersensitivity reactions.^[Ref]

Psychiatric

• Common (1% to 10%): Sleep disturbance
• Uncommon (0.1% to 1%): Bad dreams, depression/emotional depression
• Postmarketing reports: Confusion, psychotic symptoms, insomnia, nervousness^[Ref]

Musculoskeletal

• Common (1% to 10%): Myalgia
• Frequency not reported: Muscle fatigue
• Postmarketing reports: Muscle cramps, arthralgia^[Ref]

Hepatic

• Uncommon (0.1% to 1%): Elevated liver enzymes (transaminases, alkaline phosphatase)^[Ref]

Reversible elevations liver enzymes occurred during treatment, and are likely the result of a hypersensitivity reaction (e.g., allergic hepatitis).^[Ref]

Hypersensitivity

• Rare (0.01% to 0.1%): Hypersensitivity/allergic reactions
• Postmarketing reports: Allergy aggravated^[Ref]

Metabolic

• Frequency not reported: Lowered glucose tolerance
• Postmarketing reports: Hyperkalemia^[Ref]

Genitourinary

• Postmarketing reports: Galactorrhea, increased blood prolactin/hyperprolactinemia, increased urination, spotty menstruation, erectile dysfunction/impotence^[Ref]

Renal

• Postmarketing reports: Renal failure^[Ref]

Endocrine

• Postmarketing reports: Gynecomastia^[Ref]

Gynecomastia occurred in older male patients on prolonged treatment, and was reversible upon discontinuation of this drug.^[Ref]

Hematologic

• Postmarketing reports: Purpura^[Ref]

Ocular

• Postmarketing reports: Blurred vision^[Ref]

See also:

Further information

Verelan 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.

Note: Medication side effects may be underreported. If you are experiencing side effects that are not listed, submit a report to the FDA by following this guide.

Medical Disclaimer