Sorine Side Effects
Generic Name: sotalol
Note: This page contains side effects data for the generic drug sotalol. It is possible that some of the dosage forms included below may not apply to the brand name Sorine.
It is possible that some side effects of Sorine may not have been reported. These can be reported to the FDA here. Always consult a healthcare professional for medical advice.
For the Consumer
Applies to sotalol: oral tablet
Other dosage forms:
As well as its needed effects, sotalol (the active ingredient contained in Sorine) may cause unwanted side effects that require medical attention.
If any of the following side effects occur while taking sotalol, check with your doctor immediately:More common
- Blurred vision
- chest pain or discomfort
- difficult or labored breathing
- dizziness, faintness, or lightheadedness when getting up from a lying or sitting position suddenly
- fast, slow, irregular, pounding, or racing heartbeat or pulse
- lightheadedness, dizziness, or fainting
- nausea and vomiting
- shortness of breath
- swelling of face, fingers, feet, or lower legs
- tightness in chest
- unusual tiredness or weakness
- Abdominal pain or swelling
- back pain
- black, tarry stools
- blood in eyes
- blood in urine
- body aches or pain
- bruising or purple areas on skin
- burning, crawling, itching, numbness, prickling, "pins and needles", or tingling feelings
- change in consciousness
- cold hands and feet
- cough or hoarseness
- coughing up blood
- decreased alertness
- decreased urine output
- difficulty in speaking
- dilated neck veins
- double vision
- ear congestion
- extreme fatigue
- feeling of warmth or heat
- fever or chills
- flushing or redness of skin, especially on face and neck
- inability to move arms, legs, or facial muscles
- inability to speak
- irregular breathing
- joint pain or swelling
- loss of voice
- lower back or side pain
- nasal congestion
- noisy breathing
- painful, burning, or difficult urination
- pounding in the ears
- runny nose
- slow speech
- sore throat
- troubled breathing
- weight gain
- Bleeding gums
- fast breathing, sometimes with wheezing
- large amount of fat in the blood
- not able to move
- pinpoint red spots on skin
- sores, ulcers, or white spots on lips or in mouth
- swollen glands
- unusual bleeding or bruising
If any of the following symptoms of overdose occur while taking sotalol, get emergency help immediately:Symptoms of overdose
- cold sweats
- cool, pale skin
- increased hunger
- no heartbeat
- slurred speech
Some sotalol side effects may not need any medical attention. As your body gets used to the medicine these side effects may disappear. Your health care professional may be able to help you prevent or reduce these side effects, but do check with them if any of the following side effects continue, or if you are concerned about them:More common
- Acid or sour stomach
- difficulty in sleeping
- lack or loss of strength
- pain in arms or legs
- stomach discomfort or upset
- Abnormal ejaculation
- decreased sexual performance or desire
- disturbed color perception
- double vision
- excess air or gas in stomach or intestines
- full feeling
- halos around lights
- loss of appetite
- loss of vision
- mood changes
- night blindness
- overbright appearance of lights
- passing gas
- skin rash
- tunnel vision
- weight changes
- difficulty in moving
- feeling of constant movement of self or surroundings
- hair loss, thinning of hair
- increased sensitivity of skin to sunlight
- itching skin
- lack of coordination
- mental depression
- muscle aching or cramping
- muscle pains or stiffness
- quick to react or overreact emotionally
- rapidly changing moods
- redness or other discoloration of skin
- sensation of spinning
- severe sunburn
For Healthcare Professionals
Applies to sotalol: intravenous solution, oral tablet
Sotalol dosages should be reduced in patients with QTc intervals of 550 msec or greater, as the incidence of torsades de pointes is approximately 10% in such patients.
Limited animal data have shown that the incidence of potentially deleterious QT prolongation and associated risk of torsades de pointes can be significantly reduced with coadministration of mexiletine.
The SWORD (Survival with Oral d-Sotalol) trial was prematurely discontinued because the overall mortality of patients with a recent acute myocardial infarction and left ventricular systolic dysfunction who received sotalol (the active ingredient contained in Sorine) was significantly greater than in those patients who received placebo.
Sotalol may significantly depress atrial inotropic activity after electrical cardioversion of atrial fibrillation.
Limited data have suggested that sotalol demonstrates "reverse use dependence", or a decreased effect of action potential prolongation at high (200 beat/min +) heart rates. Small in vivo studies in humans have not confirmed this potential lack of efficacy, but more data are needed.
Cardiovascular arrhythmias are the most serious side effects and are usually observed within one week of therapy initiation or dosage increases. Sotalol may prolong the QT interval in 5% of patients, and may induce arrhythmias, including torsades de pointes in 1% to 5% of patients. A proarrhythmic effect is more likely in female patients, in patients who present with sustained ventricular tachycardia or fibrillation, congestive heart failure, pre-existing QT prolongation, bradycardia, or hypokalemia, or patients who receive > 320 mg/day. Sustained ventricular tachycardia or fibrillation is reported in 0.8% of patients. Sinus bradycardia is reported in up to 13% of patients and predisposes patients to torsades de pointes.
Less common cardiovascular problems include worsened or new congestive heart failure in 0.4% to 3.3%, hypotension in 2%, and sinus arrest or AV block in 1% of patients.
Nervous system complaints are mainly limited to general fatigue, headache, or dizziness in up to 15% of patients. One case of sotalol-related depression has been reported.
Respiratory problems are mainly limited to dyspnea in 1% to 7% of patients. Like other beta-blockers, sotalol (the active ingredient contained in Sorine) may inhibit beta-mediated bronchodilatory mechanisms, inducing wheezing in some patients with reactive airways disease.
Gastrointestinal side effects include diarrhea, nausea, and vomiting in 1% to 5% of patients.
Metabolic changes are mainly limited to increased total serum triglycerides. Limited data show decreased HDL cholesterol associated with sotalol (the active ingredient contained in Sorine) therapy. It is recommended that sotalol not be used in patients with preexisting hypokalemia or hypomagnesemia since these conditions may contribute to the proarrhythmic effects of sotalol.
Six cases of sclerodermatous changes associated with sotalol (the active ingredient contained in Sorine) therapy in patients with hyperthyroidism are reported.
Dermatologic side effects are uncommon. Two to 5% of patients develop a rash during sotalol therapy.
Musculoskeletal side effects are extremely rare. Cases of retroperitoneal fibrosis, proximal muscle weakness, and facial atrophy associated with sotalol (the active ingredient contained in Sorine) are reported.
A 55-year-old woman who was taking sotalol for hypertension developed a fever and bilateral hydronephrosis associated with retroperitoneal fibrosis which obstructed both ureters.
A 68-year-old woman with exertional angina pectoris developed proximal extremity weakness associated with elevated skeletal muscle creatine kinase 6 months after starting sotalol 80 mg every 8 hours. The problem persisted despite substitution with propranolol, and resolved when both drugs were withheld.
A 44-year-old man who was taking sotalol for hypertension developed facial atrophy after exposure to sub-zero weather. His facial muscle atrophy and edema were thought to be due to ischemia caused by the combined vasoconstrictive effects of the cold and beta-blockade.
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