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Dienoestrol 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:

Amitriptyline

  • Adverse Effect: Attenuation of antidepressant effectiveness; Amitriptyline toxicity (drowsiness, hypotension, akathisia)  
  • Clinical Management: If signs or symptoms of altered Amitriptyline response are noted, dose adjustment downward of either Dienoestrol or Amitriptyline may be successful in restoring effectiveness or resolving toxicity. However, drug withdrawal may be required.

    Amoxapine

  • Adverse Effect: Attenuation of antidepressant effectiveness; tricyclic toxicity (drowsiness, hypotension, akathisia)  
  • Clinical Management: If signs or symptoms of altered Amoxapine response is noted, dose adjustment downward of either Dienoestrol or Amoxapine may be successful in restoring effectiveness or resolving toxicity. However, drug withdrawal may be required.

    Chlordiazepoxide

  • Adverse Effect: Attenuation of antidepressant effectiveness; tricyclic toxicity (drowsiness, hypotension, akathisia)  
  • Clinical Management: If signs or symptoms of altered tricyclic response are noted, dose adjustment downward of either Dienoestrol or Chlordiazepoxide may be successful in restoring effectiveness or resolving toxicity. However, drug withdrawal may be required.

    Clomipramine

  • Adverse Effect: attenuation of antidepressant effectiveness; tricyclic toxicity (drowsiness, hypotension, akathisia)  
  • Clinical Management: If signs or symptoms of altered tricyclic response are noted, dose adjustment downward of either Dienoestrol or Clomipramine may be successful in restoring effectiveness or resolving toxicity. However, drug withdrawal may be required.

    Dothiepin

  • Adverse Effect: attenuation of antidepressant effectiveness; tricyclic toxicity (drowsiness, hypotension, akathisia)  
  • Clinical Management: If signs or symptoms of altered tricyclic response are noted, dose adjustment downward of either Dienoestrol or Dothiepin may be successful in restoring effectiveness or resolving toxicity. However, drug withdrawal may be required.

    Doxepin

  • Adverse Effect: attenuation of antidepressant effectiveness; tricyclic toxicity (drowsiness, hypotension, akathisia)  
  • Clinical Management: If signs or symptoms of altered tricyclic response are noted, dose adjustment downward of either Dienoestrol or Doxepin may be successful in restoring effectiveness or resolving toxicity. However, drug withdrawal may be required.

    Imipramine

  • Adverse Effect: Attenuation of antidepressant effectiveness; Imipramine toxicity (drowsiness, hypotension, akathisia)  
  • Clinical Management: If signs or symptoms of altered Imipramine response is noted, dose adjustment downward of either Dienoestrol or Imipramine may be successful in restoring effectiveness or resolving toxicity. However, drug withdrawal may be required.

    Nitroxazapine

  • Adverse Effect: attenuation of antidepressant effectiveness; tricyclic toxicity (drowsiness, hypotension, akathisia)  
  • Clinical Management: If signs or symptoms of altered tricyclic response are noted, dose adjustment downward of either Dienoestrol or Nitroxazapine may be successful in restoring effectiveness or resolving toxicity. However, drug withdrawal may be required.

    Nortriptyline

  • Adverse Effect: Attenuation of antidepressant effectiveness; tricyclic toxicity (drowsiness, hypotension, akathisia)  
  • Clinical Management: If signs or symptoms of altered Nortriptyline response are noted, dose adjustment downward of either Dienoestrol or Nortriptyline may be successful in restoring effectiveness or resolving toxicity. However, drug withdrawal may be required.

    Trimipramine

  • Adverse Effect: attenuation of antidepressant effectiveness; tricyclic toxicity (drowsiness, hypotension, akathisia)  
  • Clinical Management: If signs or symptoms of altered tricyclic response are noted, dose adjustment downward of either Dienoestrol or Trimipramine may be successful in restoring effectiveness or resolving toxicity. However, drug withdrawal may be required.
  • Dapsone
    DeferoxamineMesylate
    DesipramineHydrochloride
    DesmopressinAcetate
    Dexamethasone(Ophthalmic Susp)
    Dexamethasone(Systemic)
    Dexamethasone(Topical)
    DextromethorphanHydrobromide
    Diazepam
    Diazoxide
    DicloxacillinSodium
    DicyclomineHydrochloride
    Didanosine
    Digoxin
    Diltiazem Hydrochloride
    Dimenhydrinate
    Dimercaprol
    Diphenhydramine Hydrochloride
    DiphtheriaAntitoxin
    Disopyramide Phosphate
    Dobutamine Hydrochloride
    Dopamine Hydrochloride
    Doxacurium Chloride
    Doxycycline
    D-Penicillamine
    Dacarbazine
    Dactinomycin
    Dalteparin
    Danazol
    Danthron
    Daunorubicin
    Dehydroemetine
    Demeclocycline
    Desferrioxamine
    Desloratadine
    Desonide
    Dextropropoxyphene
    Diclofenac
    Dicyclomine - Antispas
    Dicyclomine - GU
    Drotaverine - Antispas
    Dienoestrol
    Diethyl Carbamazine
    Dihydroergotoxine
    Dilazep
    Diloxanide Furoate
    Dimethindine
    Dinoprostone
    Diosmin
    Diphenoxylate
    Dipivefrine
    Dipyridamole
    Disodium Hydrogen Citrate
    Disulfiram
    Dithranol
    Docetaxel
    Docusate Sodium
    Domperidone - Antispas
    Donepezil
    Dothiepin
    Doxapram Hydrochloride
    Doxazosin
    Doxepin
    Doxorubicin
    Doxylamine succinate
    Droperidol
    Drotaverine
    Dual Antigen
    Dydrogesterone
     
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