Help | Scores |Exit
Fragmin | Magnex | Solu Medrol
Sotalol Drug Name:  
A|B|C|D|E|F|G|H|I|K|L|M|N|O|P|Q|R|S|T|V|Z
Dosages
Indications
Interactions
Precautions
Contraindications
Adverse Reactions
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Interactions:

Adrenaline

  • Adverse Effect: Hypertension, bradycardia, resistance to Adrenaline in anaphylaxis  
  • Clinical Management: Concurrent use should be avoided if possible. However, if used concurrently, monitor blood pressure carefully. If a nonselective Sotalol causes resistance to Adrenaline in anaphylactic shock, glucagon may be effective in a dose of 1 mg or more intravenously every five minutes.

    Amiodarone

  • Adverse Effect: an increased risk of cardiotoxicity (QT prolongation, torsades de pointes, cardiac arrest)  
  • Clinical Management: The concurrent administration of sotalol and Amiodarone is not recommended. The Amiodarone should be withheld for at least three half-lives prior to dosing with sotalol.

    Amitriptyline

  • Adverse Effect: Increased risk of cardiotoxicity (QT prolongation, torsades de pointes, cardiac arrest)  
  • Clinical Management: The concurrent administration of sotalol and Amitriptyline is not recommended.

    Amoxapine

  • Adverse Effect: Increased risk of cardiotoxicity (QT prolongation, torsades de pointes, cardiac arrest)  
  • Clinical Management: The concurrent administration of sotalol and Amoxapine is not recommended.

    Antacids Comb.

  • Adverse Effect: Decreased sotalol serum concentrations and efficacy  
  • Clinical Management: Antacids should be administered at least two hours after sotalol dosing.

    Astemizole

  • Adverse Effect: an increased risk of QT prolongation and ventricular arrhythmias  
  • Clinical Management: Concomitant therapy with astemizole and sotalol should be undertaken with caution. Monitor patients closely for changes in the ECG.

    Bupivacaine Comb.

  • Adverse Effect: an increased risk of cardiotoxicity (QT prolongation, torsades de pointes, cardiac arrest)  
  • Clinical Management: The concurrent administration of sotalol and a phenothiazine is not recommended

    Celecoxib

  • Adverse Effect: Decreased antihypertensive effect  
  • Clinical Management: If concurrent therapy is required, monitor the patients blood pressure carefully and assess the need for a dosage adjustment for the beta blocker.

    Chlordiazepoxide

  • Adverse Effect: an increased risk of cardiotoxicity (QT prolongation, torsades de pointes, cardiac arrest)  
  • Clinical Management: The concurrent administration of sotalol and Chlordiazepoxide is not recommended.

    Cisapride

  • Adverse Effect: cardiotoxicity (QT prolongation, torsades de pointes, cardiac arrest)  
  • Clinical Management: The concurrent use of cisapride and Sotalol is contraindicated.

    Clomipramine

  • Adverse Effect: an increased risk of cardiotoxicity (QT prolongation, torsades de pointes, cardiac arrest)  
  • Clinical Management: The concurrent administration of sotalol and Clomipramine is not recommended.

    Clonidine

  • Adverse Effect: exaggerated clonidine withdrawal response (acute hypertension)  
  • Clinical Management: Patients to be withdrawn from clonidine who are concomitantly receiving a beta blocking agent should be monitored carefully for hypertension. Withdraw the beta blocker several days before a gradual lowering of clonidine doses. Alternatively, substitute labetalol (an alpha/beta blocker) for clonidine. Labetalol (800 to 1200 mg) should be titrated to individual patient needs based on blood pressure monitoring. In case of hypertensive crisis, alpha adrenergic blocking agents, such as phentolamine and prazosin, may be used.

    Digoxin

  • Adverse Effect: AV block and possible digoxin toxicity  
  • Clinical Management: When beta blockers and digoxin are to be given concomitantly, carefully monitor ECG and digoxin serum concentrations. Adjust doses accordingly.

    Diltiazem

  • Adverse Effect: Hypotension, bradycardia, AV conduction disturbances  
  • Clinical Management: If concurrent therapy is required, monitor cardiac function carefully, particularly in patients predisposed to heart failure. A dosage adjustment for hepatically metabolized beta blockers may be required.

    Disopyramide

  • Adverse Effect: Increased risk of cardiotoxicity (QT prolongation, torsades de pointes, cardiac arrest)  
  • Clinical Management: The concurrent administration of sotalol and Disopyramide is not recommended. The Disopyramide should be withheld for at least three half-lives prior to dosing with sotalol.

    Dothiepin

  • Adverse Effect: an increased risk of cardiotoxicity (QT prolongation, torsades de pointes, cardiac arrest)  
  • Clinical Management: The concurrent administration of sotalol and Dothiepin is not recommended.

    Doxepin

  • Adverse Effect: Increased risk of cardiotoxicity (QT prolongation, torsades de pointes, cardiac arrest)  
  • Clinical Management: The concurrent administration of sotalol and Doxepin is not recommended.

    Fentanyl

  • Adverse Effect: Severe hypotension  
  • Clinical Management: Concurrent use of a calcium channel blocker and a beta-adrenergic blocker during fentanyl anesthesia has been reported to result in severe hypotension.

    Flunarizine

  • Adverse Effect: Hypotension, bradycardia, and AV conduction disturbances  
  • Clinical Management: If concurrent therapy is required, monitor cardiac function carefully, particularly in patients predisposed to heart failure or bradyarrhythmias.

    Fluphenazine

  • Adverse Effect: an increased risk of cardiotoxicity (QT prolongation, torsades de pointes, cardiac arrest)  
  • Clinical Management: The concurrent administration of sotalol and a phenothiazine is not recommended.

    Flurbiprofen

  • Adverse Effect: Decreased antihypertensive effect  
  • Clinical Management: If concurrent therapy is required, monitor the patients blood pressure carefully and assess the need for a dosage adjustment for the beta blocker.

    Ibuprofen

  • Adverse Effect: Decreased antihypertensive effect  
  • Clinical Management: If concurrent therapy is required, monitor the patients blood pressure carefully and assess the need for a dosage adjustment for the beta blocker.

    Ibuprofen Comb.

  • Adverse Effect: Decreased antihypertensive effect  
  • Clinical Management: If concurrent therapy is required, monitor the patients blood pressure carefully and assess the need for a dosage adjustment for the beta blocker.

    Imipramine

  • Adverse Effect: Increased risk of cardiotoxicity (QT prolongation, torsades de pointes, cardiac arrest)  
  • Clinical Management: The concurrent administration of sotalol and Imipramine is not recommended.

    Indomethacin

  • Adverse Effect: Decreased antihypertensive effect  
  • Clinical Management: If concurrent therapy is required, monitor the patients blood pressure carefully and assess the need for a dosage adjustment for the beta blocker.

    Ketoprofen

  • Adverse Effect: Decreased antihypertensive effect  
  • Clinical Management: If concurrent therapy is required, monitor the patients blood pressure carefully and assess the need for a dosage adjustment for the beta blocker.

    Ketorolac

  • Adverse Effect: Decreased antihypertensive effect  
  • Clinical Management: If concurrent therapy is required, monitor the patients blood pressure carefully and assess the need for a dosage adjustment for the beta blocker.

    Lidoflazine

  • Adverse Effect: Hypotension, bradycardia, and AV conduction disturbances  
  • Clinical Management: If concurrent therapy is required, monitor cardiac function carefully, particularly in patients predisposed to heart failure or bradyarrhythmias.

    Mefenamic Acid

  • Adverse Effect: Decreased antihypertensive effect  
  • Clinical Management: If concurrent therapy is required, monitor the patients blood pressure carefully and assess the need for a dosage adjustment for the beta blocker.

    Meloxicam

  • Adverse Effect: Decreased antihypertensive effect  
  • Clinical Management: If concurrent therapy is required, monitor the patients blood pressure carefully and assess the need for a dosage adjustment for the beta blocker.

    Methyldopa

  • Adverse Effect: Exaggerated hypertensive response, tachycardia, or arrhythmias during physical stress or exposure to exogenous catecholamines  
  • Clinical Management: Monitor blood pressure carefully during concurrent therapy, especially during excessive physiologic stress or use of exogenous catecholamines such as phenylpropanolamine.

    Nabumetone

  • Adverse Effect: Decreased antihypertensive effect  
  • Clinical Management: If concurrent therapy is required, monitor the patients blood pressure carefully and assess the need for a dosage adjustment for the beta blocker.

    Naproxen

  • Adverse Effect: Decreased antihypertensive effect  
  • Clinical Management: If concurrent therapy is required, monitor the patients blood pressure carefully and assess the need for a dosage adjustment for the beta blocker.

    Nimesulide

  • Adverse Effect: Decreased antihypertensive effect  
  • Clinical Management: If concurrent therapy is required, monitor the patients blood pressure carefully and assess the need for a dosage adjustment for the beta blocker.

    Nortriptyline

  • Adverse Effect: Increased risk of cardiotoxicity (QT prolongation, torsades de pointes, cardiac arrest)

    Oxyphenbutazone

  • Adverse Effect: Decreased antihypertensive effect  
  • Clinical Management: If concurrent therapy is required, monitor the patients blood pressure carefully and assess the need for a dosage adjustment for the beta blocker.

    Paracetamol

  • Adverse Effect: Decreased antihypertensive effect  
  • Clinical Management: If concurrent therapy is required, monitor the patients blood pressure carefully and assess the need for a dosage adjustment for the beta blocker.

    Paracetamol Comb.

  • Adverse Effect: Decreased antihypertensive effect  
  • Clinical Management: If concurrent therapy is required, monitor the patients blood pressure carefully and assess the need for a dosage adjustment for the beta blocker.

    Phenacetin

  • Adverse Effect: Decreased antihypertensive effect  
  • Clinical Management: If concurrent therapy is required, monitor the patients blood pressure carefully and assess the need for a dosage adjustment for the beta blocker.

    Phenylbutazone

  • Adverse Effect: Decreased antihypertensive effect  
  • Clinical Management: If concurrent therapy is required, monitor the patients blood pressure carefully and assess the need for a dosage adjustment for the beta blocker.

    Pimozide

  • Adverse Effect: an increased risk of cardiotoxicity (QT prolongation, torsades de pointes, cardiac arrest)  
  • Clinical Management: Pimozide is contraindicated in individuals with congenital QT syndrome, patients with a history of cardiac arrhythmias, or patients taking other drugs which may prolong the QT interval.

    Piroxicam

  • Adverse Effect: Decreased antihypertensive effect  
  • Clinical Management: If concurrent therapy is required, monitor the patients blood pressure carefully and assess the need for a dosage adjustment for the beta blocker.

    Prazosin - BPH

  • Adverse Effect: An exaggerated hypotensive response to the first dose of the alpha blocker  
  • Clinical Management: When concurrent therapy with an alpha blocker and a beta blocker is required, initiate the alpha blocker with a smaller than usual dose, preferably at bedtime. Monitor the patient closely for hypotension.

    Procainamide

  • Adverse Effect: an increased risk of cardiotoxicity (QT prolongation, torsades de pointes, cardiac arrest)  
  • Clinical Management: The concurrent administration of sotalol and Procainamide is not recommended. The Procainamide should be withheld for at least three half-lives prior to dosing

    Quinidine

  • Adverse Effect: Increased risk of cardiotoxicity (QT prolongation, torsades de pointes, cardiac arrest)  
  • Clinical Management: The concurrent administration of sotalol and Quinidine is not recommended. The Quinidine should be withheld for at least three half-lives prior to dosing with sotalol.

    Ritodrine

  • Adverse Effect: Potential interference with tocolytic action of ritodrine  
  • Clinical Management: It is possible to successfully treat a patient with both a beta blocker and a beta mimetic if an appropriate dosage is found and the clinical response is monitored.

    Sparfloxacin

  • Adverse Effect: prolongation of the QTc interval and/or torsades de pointes  
  • Clinical Management: Sparfloxacin is contraindicated in individuals with known QTc prolongation or in patients being treated concurrently with drugs that are known to increase the QTc interval and/or cause torsades de pointes.

    Tenoxicam

  • Adverse Effect: Decreased antihypertensive effect  
  • Clinical Management: If concurrent therapy is required, monitor the patients blood pressure carefully and assess the need for a dosage adjustment for the beta blocker.

    Terazosin - BPH

  • Adverse Effect: An exaggerated hypotensive response to the first dose of the alpha blocker  
  • Clinical Management: When concurrent therapy with an alpha blocker and a beta blocker is required, initiate the alpha blocker with a smaller than usual dose, preferably at bedtime. Monitor the patient closely for hypotension.

    Terfenadine

  • Adverse Effect: ventricular arrhythmias  
  • Clinical Management: Concurrent use of sotalol and terfenadine is not recommended because both drugs are known to prolong the QT interval.

    Thioridazine

  • Adverse Effect: an increased risk of cardiotoxicity (QT prolongation, torsades de pointes, cardiac arrest)  
  • Clinical Management: The concurrent administration of sotalol and a phenothiazine is not recommended.

    Trifluoperazine

  • Adverse Effect: Increased risk of cardiotoxicity (QT prolongation, torsades de pointes, cardiac arrest)  
  • Clinical Management: The concurrent administration of sotalol and a Trifluoperazine is not recommended.

    Trimipramine

  • Adverse Effect: an increased risk of cardiotoxicity (QT prolongation, torsades de pointes, cardiac arrest)  
  • Clinical Management: The concurrent administration of sotalol and Trimipramine is not recommended.

    Verapamil

  • Adverse Effect: Hypotension, bradycardia  
  • Clinical Management: If concurrent therapy is required, monitor cardiac function carefully, particularly in patients predisposed to heart failure.
  • Salmeterol Xinafoate
    Silver Nitrate
    Sodium Bicarbonate
    Sodium Fluoride
    Sodium Phosphates
    Somatropin
    Spironolactone
    Stavudine
    Streptomycin Sulfate
    Sulfacetamide Sodium
    Sulfasalazine
    Sulfisoxazole
    Saccharine
    Saccharomyces
    Salbutamole
    Salbutamole - inh
    Salicylates
    Salmeterol - inh
    Satranidazole
    Sacnidazole
    Selegiline
    Senna
    Serratiopeptidase
    Sertraline
    Sibutramine
    Sildenafil citrate
    Silver Sulfadiazine - Ocular
    Silver Sulphadiazine
    Silymarin
    Simvastatin
    Sisomicin
    Sisomicin - Ocular
    Snake Venom Antisera
    Sod Picosulphate
    Sodium Antimony Gluconate
    Sodium Cromoglycate
    Sodium Cromoglycate - Inh
    Sodium Cromoglycate - Ocular
    Sodium Fusidate
    Sodium Hyaluronate
    Sodium Nitroprusside
    Sodium Valproate
    Sodium tetradecyl
    Soframycin - Ocular
    Somatostatin
    Sotalol
    Sparfloxacin
    Spectinomycin
    Spiramycin
    Stanozolol
    Streptokinase
    Streptomycin
    Succinyl Choline
    Sucralfate
    Sulbutiamine
    Sulfonamide - VU
    Sulphacetamide - Ocular
    Sulphadiazine
    Sulphamethizole
    Sulphasalazine-Antisecr
    Sumatriptan
     
    Disclaimer