Reboxetine- @Selective noradrenaline reuptake inhibitor
Drug Name:
Reboxetine- @Selective noradrenaline reuptake inhibitor
List Of Brands:
Indication Type Description:
Pharmacology/ Pharmacokinetics
Drug Interaction:
Selective serotonin reuptake inhibitors includ- Fluoxetine, Fluvoxamine, Paroxetine, Sertraline, Citalopram, Escitalopram Refer- Fluoxetine
Avoid concurrent administration with antiarrhythmics, antipsychotics, cyclosporin, imidazole and triazole antifungals,tricyclic antidepressants Concurrentuse with CYP3A4 inhibitors may increase plasmalevels of reboxetine. Concurrent use with ergot alkaloids may increase BP. Risk of hyperetensive crisis, when used with MAOIs
Indication:
New Drugs Approved by (DCI) Drug Controller GENERAL - India For Marketing
(Ref- IDMA Publication)
Name of Drug Indication Date of Approval
Reboxetine Anti-depressant 31-12-2002
Depressive illness
Adverse Reaction:
Insominia, dizziness, increase sweating, impotence Dry mouth, constipation, urinary hesistency, postural hypotension, dysuria, parethesia, hyponatremia tachycardia
Contra-Indications:
Special pecautions-
Renal and hepatic impairment, benign prostatic hyperplasia cardiac disorders, epilepsy bipolar disorders urinary retension, glaucoma may impair ability to perform tasks, driving or operating machinery, Monitor for signs of clinical worsening eg. suicidal tendency esp during th initial phase of treatment
Dosages/ Overdosage Etc:
Indications:
Depressive illness
Dosage
Typical 8-10mg daily
Patient Information:
Selective serotonin reuptake inhibitors includ- Fluoxetine, Fluvoxamine, Paroxetine, Sertraline, Citalopram, Escitalopram Refer- Fluoxetine
Pharmacology/ Pharmacokinetics:
Pharmacology:
Roboxtetine selectively and potentially inhibits norephinephrine reuptake.It has been shown to have negligable affinity for serotonin and dopamine uptake sites for adrenergic and histaminergic receptors, and only weak affinity for muscarinic receptors.
Pharmacokinetics:
It is rapidly absorbed after oral administration. The tmax is about 2hrs and terminal half-life of elimination is 13 hrs, allowing a twice daily administration. Elimination is principally by renal route.
Pregnancy and lactation:
Use with caution during pregnancy and lactation.