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Felodipine Drug Name:  
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Indications
Dosages
Interactions
Precautions
Contraindications
Adverse Reactions
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Interactions:

Acenocoumarol

  • Adverse Effect: an increased risk of gastrointestinal hemorrhage  
  • Clinical Management: Patients who are receiving concurrent Felodipine 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 Felodipine should be avoided in patients with sick sinus syndrome or partial AV (atrioventricular) block.

    Atenolol

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

    Betaxolol

  • Adverse Effect: hypotension and/or bradycardia  
  • Clinical Management: If concurrent therapy is required, monitor cardiac function carefully, particularly in patients predisposed to heart failure.

    Bisoprolol

  • Adverse Effect: hypotension and/or bradycardia  
  • Clinical Management: If concurrent therapy is required, monitor cardiac function carefully, particularly in patients predisposed to heart failure.

    Carbamazepine

  • Adverse Effect: Decreased felodipine effectiveness  
  • Clinical Management: Monitor clinical response to felodipine with dose adjustments as needed to achieve or maintain cardiovascular response. Felodipine does not appear to interact with carbamazepine and may be considered as an alternative to felodipine.

    Carvedilol

  • Adverse Effect:hypotension and/or bradycardia  
  • Clinical Management: If concurrent therapy is required, monitor cardiac function carefully, particularly in patients predisposed to heart failure.

    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 and/or bradycardia  
  • Clinical Management: If concurrent therapy is required, monitor cardiac function carefully, particularly in patients predisposed to heart failure.  

    Digoxin

  • Adverse Effect: Transient increases in the digoxin serum concentration  
  • Clinical Management: Monitor the patient for signs of digoxin toxicity (nausea, vomiting, arrhythmias) when felodipine therapy is initiated. This especially applies to a patient who is already in the upper therapeutic digoxin concentration range or who is renally impaired.

    Erythromycin

  • Adverse Effect: Felodipine toxicity (flushing, edema, tachycardia)  
  • Clinical Management: If concurrent therapy is required, monitor for felodipine toxicity (eg, tachycardia, edema, flushing). If adverse effects occur, either discontinue the use of erythromycin or lower the dose of felodipine and monitor the response.  

    Esmolol

  • Adverse Effect: hypotension and/or bradycardia  
  • Clinical Management: If concurrent therapy is required, monitor cardiac function carefully, particularly in patients predisposed to heart failure.  

    Fluconazole

  • Adverse Effect: Increased felodipine serum concentrations and toxicity (dizziness, hypotension, flushing, headache, peripheral edema)  
  • Clinical Management: Observe for development of toxicity associated with the calcium channel blocker (peripheral edema, dizziness, hypotension, flushing, headache). Consider reducing the dose of Felodipine or withdrawing one of the agents.

    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.

    Indinavir

  • Adverse Effect: increase in the Plasma concentration of Calcium Channel Blockers like Felodipine due to inhibition of cytochrome P450 3A4  
  • Clinical Management: Monitor for the adverse effect and administer the drugs with caution.

    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.

    Itraconazole

  • Adverse Effect: Increased felodipine serum concentrations and toxicity (dizziness, hypotension, flushing, headache, peripheral edema)  
  • Clinical Management: The concurrent use of itraconazole and felodipine should be avoided. If these agents must be used together, observe for development of toxicity associated with felodipine (peripheral edema, dizziness, hypotension, flushing, headache). Substantial decreases in the felodipine dose may be necessary.

    Ketoconazole

  • Adverse Effect: increased Felodipine serum concentrations and toxicity (dizziness, hypotension, flushing, headache, peripheral edema)  
  • Clinical Management: Observe for development of toxicity associated with Felodipine (peripheral edema, dizziness, hypotension, flushing, headache). Consider reducing the dose of Felodipine or withdrawing one of the agents.

    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 and/or bradycardia  
  • Clinical Management: If concurrent therapy is required, monitor cardiac function carefully, particularly in patients predisposed to heart failure.  

    Levobunolol

  • Adverse Effect: hypotension and/or bradycardia  
  • Clinical Management: If concurrent therapy is required, monitor cardiac function carefully, particularly in patients predisposed to heart failure.  

    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 and/or bradycardia  
  • Clinical Management: If concurrent therapy is required, monitor cardiac function carefully, particularly in patients predisposed to heart failure.

    Mg. salts

  • Adverse Effect: Hypotension  
  • Clinical Management: Monitor blood pressure closely when adding or deleting Felodipine in patients receiving magnesium.  

    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.  

    Oxcarbazepine

  • Adverse Effect: Felodipine AUC was lowered  
  • Clinical Management: Monitor for therapeutic effects and adjust the dose accordingly.

    Oxprenolol

  • Adverse Effect: hypotension and/or bradycardia  
  • Clinical Management: If concurrent therapy is required, monitor cardiac function carefully, particularly in patients predisposed to heart failure.

    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 Felodipine and Phenindione should be monitored for excessive bleeding, especially from the gastrointestinal tract.

    Phenobarbitone

  • Adverse Effect: Decreased felodipine effectiveness  
  • Clinical Management: Monitor patient for loss of Felodipine effects, including clinical signs or symptoms of hypertension or angina. Dose increases may be required.

    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.

    Phenytoin

  • Adverse Effect: Decreased felodipine effectiveness  
  • Clinical Management: Monitor for continuing clinical effectiveness of felodipine. Larger than expected doses may be required. Other Felodipine may be tried cautiously since some of these agents have been shown to interact with phenytoin to produce symptomatic, toxic elevations in serum phenytoin levels. Use of an alternative therapeutic class of drug (ACE inhibitors, for example) may be required to minimize the possibility for a phenytoin interaction.

    Pindolol

  • Adverse Effect: hypotension and/or bradycardia  
  • Clinical Management: If concurrent therapy is required, monitor cardiac function carefully, particularly in patients predisposed to heart failure.

    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 and/or bradycardia  
  • Clinical Management: If concurrent therapy is required, monitor cardiac function carefully, particularly in patients predisposed to heart failure.

    Rifampicin

  • Adverse Effect: Decreased felodipine efficacy

    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.

    Theophylline

  • Adverse Effect: A decrease of theophylline efficacy  
  • Clinical Management: Theophylline serum concentrations should be closely monitored when felodipine is added, discontinued, or when dosing changes occur. Dosing adjustments of theophylline may be necessary.

    Timolol

  • Adverse Effect: hypotension and/or bradycardia  
  • Clinical Management: If concurrent therapy is required, monitor cardiac function carefully, particularly in patients predisposed to heart failure.

    Warfarin

  • Adverse Effect: an increased risk of gastrointestinal hemorrhage  
  • Clinical Management: Patients who are receiving concurrent Felodipine and Warfarin should be monitored for excessive bleeding, especially from the gastrointestinal tract.
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    FerrousFumarate
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    FerrousSulfate
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    Fluconazole
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    FluoxetineHydrochloride
    FluticasonePropionate
    FolicAcid
    FoscarnetSodium(Phosphonoformic Acid)
    Furosemide
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