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

Molecule : Alprazolam

  • Adverse Effect: alprazolam toxicity (CNS depression, ataxia, lethargy)  
  • Clinical Management: With concurrent administration, monitor patients for CNS depression.Consider switching to lorazepam, oxazepam, temazepam.  

    Molecule : Ampicillin

  • Adverse Effect: Reduced ampicillin bioavailability  
  • Clinical Management: Monitor the patient for ampicillin efficacy if omeprazole is being using concurrently.  

    Molecule : Carbamazepine

  • Adverse Effect: An increased risk of carbamazepine toxicity  
  • Clinical Management: Monitor patients receiving concurrent carbamazepine and omeprazole therapy for signs of carbamazepine toxicity (ataxia, nystagmus, diplopia, headache, vomiting, apnea, seizures, coma). Also monitor carbamazepine serum levels. Doses of carbamazepine may need to be reduced.  

    Molecule : Clarithromycin

  • Adverse Effect: Increased bioavailability of both agents  

    Molecule : Diazepam

  • Adverse Effect: Enhanced and prolonged diazepam effects  
  • Clinical Management: Monitor for signs of excessive Diazepam effects (eg, sedation, dizziness, ataxia, weakness, decreased cognition or motor performance). If symptoms are present, reduce diazepam dose or consider switching to a Diazepam eliminated by glucuronidation (eg, lorazepam, oxazepam, temazepam).  

    Molecule : Digoxin

  • Adverse Effect: Digoxin toxicity (vomiting, cardiac arrhythmias)  
  • Clinical Management: Monitor patient for signs of digoxin toxicity and adjust digoxin dose if necessary.  

    Molecule : Disulfiram

  • Adverse Effect: disulfiram toxicity (confusion, disorientation, psychotic changes)  
  • Clinical Management: Closely monitor patient response with special attention to mental status changes when coadministering disulfiram and omeprazole. Dose reductions in either or both agents may be needed.  

    Molecule : Itraconazole

  • Adverse Effect: loss of itraconazole efficacy  
  • Clinical Management: Itraconazole should be administered with a cola beverage in patients receiving Omeprazole.  

    Molecule : Ketoconazole

  • Adverse Effect: loss of ketoconazole efficacy  
  • Clinical Management: Concurrent administration of ketoconazole and Omeprazole should be undertaken with caution. If concurrent use cannot be avoided, aggressively monitor these patients for continued antifungal efficacy.  

    Molecule : Methotrexate

  • Adverse Effect: an increased risk of methotrexate toxicity  
  • Clinical Management: Closely monitor patients receiving omeprazole and methotrexate concurrently. Omeprazole may have to be temporarily discontinued.  

    Molecule : Midazolam

  • Adverse Effect: Midazolam toxicity (CNS depression, ataxia, lethargy)  
  • Clinical Management: With concurrent administration, monitor patients for CNS depression (sedation, lethargy, speech difficulties), and adjust doses accordingly.Switch to lorazepam, oxazepam, temazepam.  

    Molecule : Olanzapine

  • Adverse Effect: Concomitant administration results in increased clearance of Olanzapine due to the induction of CYP1A2 or glucuronyl transferase enzyme  
  • # Clinical Management: Monitor for the therapeutic effects and adjust the dose accordingly.  

    Molecule : Phenytoin

  • Adverse Effect: An increased risk of phenytoin toxicity (ataxia, hyperreflexia, nystagmus, tremor)  
  • Clinical Management: Monitor patients for phenytoin toxicity with concomitant omeprazole use; serum phenytoin levels might also be considered, particularly with doses of omeprazole greater than 20 milligrams daily. Adjust phenytoin dosage as needed.  

    Molecule : Rifampicin

  • Adverse Effect: Concomitant administration results in increased clearance of Olanzapine due to the induction of CYP1A2 or glucuronyl transferase enzyme  
  • # Clinical Management: Monitor for the therapeutic effects and adjust the dose accordingly.  

    Molecule : Ticlopidine

  • Adverse Effect: increased omeprazole bioavailability  

    Molecule : Warfarin

  • Adverse Effect: An increased risk of bleeding  
  • Clinical Management: In patients receiving oral anticoagulant therapy with warfarin, the prothrombin time ratio or international normalized ratio (INR) should be closely monitored with the addition and withdrawal of treatment with omeprazole, and should be reassessed periodically during concurrent therapy. Adjustments of the warfarin dose may be necessary in order to maintain the desired level of anticoagulation.
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