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Flunarizine Drug Name:  
A|B|C|D|E|F|G|H|I|K|L|M|N|O|P|Q|R|S|T|V|Z
Indications
Dosages
Interactions
Precautions
Contraindications
Adverse Reactions
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Interactions:

Acenocoumarol

  • Adverse Effect: Increased risk of gastrointestinal hemorrhage  
  • Clinical Management: Patients who are receiving concurrent Flunarizine and Acenocoumarol should be monitored for excessive bleeding, especially from the gastrointestinal tract.

    Amiodarone

  • Adverse Effect: Atrioventricular block and slowing of sinus rate  
  • Clinical Management: Concurrent use of amiodarone and Flunarizine should be avoided in patients with sick sinus syndrome or partial AV (atrioventricular) block.

    Atenolol

  • 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.

    Betaxolol

  • 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.

    Bisoprolol

  • 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.

    Carbamazepine

  • Adverse Effect: Increased carbamazepine serum levels and possible toxicity (ataxia, nystagmus, diplopia, headache, vomiting, apnea, seizures, coma)  
  • Clinical Management: Continue routine monitoring of carbamazepine serum levels. Some dose adjustment may be needed if both clinical symptoms and laboratory findings suggest carbamazepine toxicity.

    Carvedilol

  • 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.

    Celecoxib

  • Adverse Effect: An increased risk of gastrointestinal hemorrhage  
  • Clinical Management: Patients who are receiving concurrent NSAID and calcium channel blocker therapy should be monitored for signs of gastrointestinal hemorrhage, such as weakness, nausea, and blood in the stool.

    Celiprolol

  • 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.

    Esmolol

  • 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.

    Flurbiprofen

  • Adverse Effect: An increased risk of gastrointestinal hemorrhage  
  • Clinical Management: Patients who are receiving concurrent NSAID and calcium channel blocker therapy should be monitored for signs of gastrointestinal hemorrhage, such as weakness, nausea, and blood in the stool.

    Ibuprofen

  • Adverse Effect: An increased risk of gastrointestinal hemorrhage  
  • Clinical Management: Patients who are receiving concurrent NSAID and calcium channel blocker therapy should be monitored for signs of gastrointestinal hemorrhage, such as weakness, nausea, and blood in the stool.

    Indomethacin

  • Adverse Effect: An increased risk of gastrointestinal hemorrhage  
  • Clinical Management: Patients who are receiving concurrent NSAID and calcium channel blocker therapy should be monitored for signs of gastrointestinal hemorrhage, such as weakness, nausea, and blood in the stool.

    Ketoprofen

  • Adverse Effect: An increased risk of gastrointestinal hemorrhage  
  • Clinical Management: Patients who are receiving concurrent NSAID and calcium channel blocker therapy should be monitored for signs of gastrointestinal hemorrhage, such as weakness, nausea, and blood in the stool.

    Ketorolac

  • Adverse Effect: An increased risk of gastrointestinal hemorrhage  
  • Clinical Management: Patients who are receiving concurrent NSAID and calcium channel blocker therapy should be monitored for signs of gastrointestinal hemorrhage, such as weakness, nausea, and blood in the stool.

    Labetalol

  • 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.

    Levobunolol

  • 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: An increased risk of gastrointestinal hemorrhage  
  • Clinical Management: Patients who are receiving concurrent NSAID and calcium channel blocker therapy should be monitored for signs of gastrointestinal hemorrhage, such as weakness, nausea, and blood in the stool.

    Meloxicam

  • Adverse Effect: An increased risk of gastrointestinal hemorrhage  
  • Clinical Management: Patients who are receiving concurrent NSAID and calcium channel blocker therapy should be monitored for signs of gastrointestinal hemorrhage, such as weakness, nausea, and blood in the stool.

    Metoprolol

  • 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.

    Nabumetone

  • Adverse Effect: An increased risk of gastrointestinal hemorrhage  
  • Clinical Management: Patients who are receiving concurrent NSAID and calcium channel blocker therapy should be monitored for signs of gastrointestinal hemorrhage, such as weakness, nausea, and blood in the stool.

    Naproxen

  • Adverse Effect: An increased risk of gastrointestinal hemorrhage  
  • Clinical Management: Patients who are receiving concurrent NSAID and calcium channel blocker therapy should be monitored for signs of gastrointestinal hemorrhage, such as weakness, nausea, and blood in the stool.

    Nimesulide

  • Adverse Effect: An increased risk of gastrointestinal hemorrhage  
  • Clinical Management: Patients who are receiving concurrent NSAID and calcium channel blocker therapy should be monitored for signs of gastrointestinal hemorrhage, such as weakness, nausea, and blood in the stool.

    Oxprenolol

  • 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.

    Oxyphenbutazone

  • Adverse Effect: An increased risk of gastrointestinal hemorrhage  
  • Clinical Management: Patients who are receiving concurrent NSAID and calcium channel blocker therapy should be monitored for signs of gastrointestinal hemorrhage, such as weakness, nausea, and blood in the stool.

    Paracetamol

  • Adverse Effect: An increased risk of gastrointestinal hemorrhage  
  • Clinical Management: Patients who are receiving concurrent NSAID and calcium channel blocker therapy should be monitored for signs of gastrointestinal hemorrhage, such as weakness, nausea, and blood in the stool.

    Phenacetin

  • Adverse Effect: An increased risk of gastrointestinal hemorrhage  
  • Clinical Management: Patients who are receiving concurrent NSAID and calcium channel blocker therapy should be monitored for signs of gastrointestinal hemorrhage, such as weakness, nausea, and blood in the stool.

    Phenindione

  • Adverse Effect: an increased risk of gastrointestinal hemorrhage  
  • Clinical Management: Patients who are receiving concurrent Flunarizine and Phenindione should be monitored for excessive bleeding, especially from the gastrointestinal tract.

    Phenylbutazone

  • Adverse Effect: An increased risk of gastrointestinal hemorrhage  
  • Clinical Management: Patients who are receiving concurrent NSAID and calcium channel blocker therapy should be monitored for signs of gastrointestinal hemorrhage, such as weakness, nausea, and blood in the stool.

    Pindolol

  • 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.

    Piroxicam

  • Adverse Effect: An increased risk of gastrointestinal hemorrhage  
  • Clinical Management: Patients who are receiving concurrent NSAID and calcium channel blocker therapy should be monitored for signs of gastrointestinal hemorrhage, such as weakness, nausea, and blood in the stool.

    Propranolol

  • 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.

    Rifampicin

  • Adverse Effect: Decreased flunarizine efficacy

    Sotalol

  • 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.

    Tenoxicam

  • Adverse Effect: An increased risk of gastrointestinal hemorrhage  
  • Clinical Management: Patients who are receiving concurrent NSAID and calcium channel blocker therapy should be monitored for signs of gastrointestinal hemorrhage, such as weakness, nausea, and blood in the stool.

    Timolol

  • 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.

    Warfarin

  • Adverse Effect: an increased risk of gastrointestinal hemorrhage  
  • Clinical Management: Patients who are receiving concurrent Flunarizine and Warfarin should be monitored for excessive bleeding, especially from the gastrointestinal tract.
  • FentanylCitrate
    FerrousFumarate
    FerrousGluconate
    FerrousSulfate
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    Fluconazole
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    Fluorouracil
    FluoxetineHydrochloride
    FluticasonePropionate
    FolicAcid
    FoscarnetSodium(Phosphonoformic Acid)
    Furosemide
    Fluorouracil-I
    Factor vlll
    Famotidine
    Felodipine
    Feracrylum
    Fexofenadine
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    Flavonoids
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    Fludarabine
    Fludrocortisone acetate
    Flunarizine
    Fluocinolone
    Fluoxetine
    Flupenthixol Decanoate
    Fluphenazine
    Flurbiprofen
    Flurbiprofen - Ocular
    Flutamide
    Fluvoxamine
    Furazolidone
     
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