Quasense

Quasense

Generic Name

Quasense

Mechanism

Quasense is a *dual‑action* oral agent that:
Inhibits reuptake of serotonin (5‑HT) and norepinephrine (NE) via selective blockade of the serotonin transporter (SERT) and norepinephrine transporter (NET).
• Exerts partial agonism at the 5‑HT₁A receptor, enhancing serotonergic tone and modulating mood and anxiety circuits.
• The combination of transporter inhibition and receptor agonism produces rapid antidepressant and anxiolytic effects with a lower incidence of sexual dysfunction compared with pure serotonin‑selective agents.

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Pharmacokinetics

  • Absorption: Oral bioavailability ~70 %; peak plasma concentration (Tₘₐₓ) at ~4–6 h.
  • Distribution: Moderate protein binding (~70 %); crosses the blood‑brain barrier efficiently.
  • Metabolism: Phase I oxidative metabolism by CYP2D6 (primary) and CYP3A4 (secondary).
  • Elimination: 40 % renal excretion unchanged; 30 % fecal; terminal half‑life 12–16 h.
  • Food Interaction: Minor; take with or without food.

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Indications

  • Major Depressive Disorder (MDD) – Adult and adolescent populations.
  • Generalized Anxiety Disorder (GAD) – Improved sleep quality and reduced somatic symptoms.
  • Chronic Neuropathic Pain – As an add‑on to opioids or anticonvulsants.
  • Off‑label: Post‑traumatic stress disorder (PTSD) in selected cases.

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Contraindications

  • Contraindicated with monoamine oxidase inhibitors (MAOIs) or within 14 days of MAOI discontinuation.
  • Caution in patients with:
  • Severe hepatic impairment (Child‑Pugh C).
  • Severe renal impairment (CrCl < 15 mL/min); dose adjustment needed.
  • Pregnancy (Category C) – limited data; weigh benefits vs. risks.
  • Warnings:
  • ↑ risk of serotonin syndrome when combined with other serotonergic drugs (e.g., triptans, tramadol).
  • Potential for QT prolongation at supratherapeutic doses.
  • Rarely, liver injury (monitor LFTs).

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Dosing

PopulationInitial DoseTitrationMax DoseNotes
Adults (MDD/GAD)50 mg PO qdIncrease 50 mg qw to 100 mg qd (within 4 weeks)150 mg qdAvoid exceeding 150 mg/qd; monitor for side effects.
Adolescents (≥12 yr)25 mg PO qdIncrease 25 mg qw to 50 mg qd (within 4 weeks)100 mg qdStart lower to minimize GI upset.
Renal impairment (CrCl ≥ 30 mL/min)50 mg PO qdSame as adults150 mg qdDose may be reduced to 25 mg qd if CrCl 15–30 mL/min.
Elderly (>65 yr)50 mg PO qdSame as adults150 mg qdConsider lower starting dose if frail or on polypharmacy.

Take with or without food; avoid grapefruit juice.
Missed dose: Take as soon as remembered; skip if next dose due in <24 h.

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Adverse Effects

Common (≥5 %):
• Nausea, dry mouth, constipation.
• Headache, dizziness, insomnia.
• Mild sexual dysfunction (decreased libido).

Serious (≤1 %):
• Serotonin syndrome (hypercreflexia, clonus, hyperthermia).
• QTc prolongation → arrhythmias (rare).
• Severe hepatocellular injury.
• Hyponatremia (especially in elderly).

Management:
• Discontinue or dose‑reduce for serotonin syndrome.
• Monitor ECG & electrolytes if high dose or multiple serotonergic agents.

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Monitoring

  • Baseline: CBC, CMP (LFTs, electrolytes), ECG if cardiovascular disease.
  • During therapy:
  • LFTs at 2 weeks, 4 weeks, then every 3 months.
  • Electrolytes annually; sooner if symptomatic.
  • Serotonin syndrome signs: evaluate at each visit.
  • Pregnancy & lactation: No mandatory surveillance, but document maternal‑fetal status.

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Clinical Pearls

1. Start Low, Go Slow: 50 mg qd minimizes early‑onset GI distress; gradual uptitration reduces breakthrough anxiety.

2. Serotonin‑Syndrome Check: Never combine Quasense with MAOIs, linezolid, or St. John’s Wort without a washout period.

3. Neuropathic Pain Synergy: Add 25–50 mg qd to gabapentin or duloxetine to harness dual pain‑modulating pathways.

4. Renal Dose Adjustment: Use 25 mg qd for CrCl 15–30 mL/min; monitoring of drug levels is not routinely required.

5. Pregnancy Precaution: If treatment is essential, weigh benefits vs risks; consider non‑motoric interventions first.

6. QTc Watchout: In patients on *cimetidine*, *ticagrelor*, or *antifungal CYP3A4 inhibitors*, check QTc after dose escalation.

7. Patient Education: Emphasize consistent daily dosing; advise immediate reporting of tremor, confusion, or slurred speech.

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Key Takeaway:

Quasense offers a balanced serotonin‑norepinephrine uptake inhibition combined with 5‑HT₁A partial agonism, making it a robust choice for *depression, anxiety,* and *neuropathic pain* with a favorable side‑effect profile when monitored appropriately.

Medical & AI Content Disclaimers
Medical Disclaimer: Medical definitions are provided for educational purposes and should not replace professional medical advice, diagnosis, or treatment.

AI Content Disclaimer: Some definitions may be AI-generated and may contain inaccuracies. Always verify with authoritative medical references.

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