
Antidepressants: SSRIs, SNRIs, Atypical Antidepressants, MAOIs
Drug Names & Dosing
1. SSRIs
Sertraline: 50 mg PO OD, ↑ to 100 mg after 7 days (max 200 mg)
Escitalopram: 10 mg PO OD (max 20 mg)
Fluoxetine: 20 mg PO OD (max 60 mg)
Fluvoxamine: 50–100 mg PO OD (max 300 mg in divided doses)
Citalopram: 20 mg PO OD (max 40 mg; max 20 mg if >65 years due to QTc risk)
Paroxetine: 20 mg PO OD (max 50 mg)
2. SNRIs
Duloxetine: 60 mg PO OD (max 120 mg)
Venlafaxine XR: 75 mg PO OD (max 375 mg; monitor BP at higher doses)
Desvenlafaxine XR: 50 mg PO OD (max 200 mg)
Reboxetine: 4 mg PO BD (max 12 mg; second-line)
3. Atypical Antidepressants
Mirtazapine: 15–30 mg PO nocte (max 60 mg; lower doses more sedating)
Agomelatine: 25 mg PO nocte (max 50 mg; requires LFT monitoring)
4. MAOIs
Selegiline: 5 mg PO BD (also for Parkinson’s disease)
Phenelzine: 15 mg PO TDS (max 90 mg; irreversible, non-selective)
Moclobemide: 150 mg PO BD (max 600 mg; reversible MAOI-A, second-line)
Pharmacological Considerations
First-Line Options: SSRIs, SNRIs, mirtazapine
Second-Line: MAOIs, reboxetine (due to safety/tolerability concerns)
MAOIs: Risk of hypertensive crisis with dietary tyramine (e.g., aged cheese, cured meats)
Special Populations:
Elderly: SSRIs preferred; avoid citalopram (>65 years) due to QTc prolongation risk
SNRIs: Venlafaxine may ↑ BP at higher doses → monitor BP
Mirtazapine: Useful for insomnia or poor appetite
Monitoring & Interactions
1. SSRIs/SNRIs
Monitor for serotonin syndrome with other serotonergic drugs (e.g., tramadol, linezolid)
Regular BP checks for venlafaxine (high doses)
2. MAOIs
Dietary Restrictions: Avoid tyramine-rich foods to prevent hypertensive crisis
Washout Periods: Strict when switching to/from other antidepressants to avoid serotonin syndrome or hypertensive crisis
3. Additional Monitoring
Monitor for weight changes
LFTs: Periodic monitoring for agomelatine
BP: Regular checks, especially with venlafaxine or SNRIs at high
Notes
Antidepressants are typically dosed once daily (OD) unless specified
Educate patients on potential interactions and the need for adherence to monitoring schedules
Antidepressants: Considerations When Prescribing
Key Considerations Before Prescribing
Symptom Assessment
Evaluate severity, duration, and impact on functioning
Comorbidities
Tailor choice based on coexisting conditions (e.g., anxiety, chronic pain, insomnia)
Drug Interactions
Review concurrent medications:
SSRIs + warfarin: Increased bleeding risk
Serotonergic agents (e.g., tramadol): Serotonin syndrome risk
Previous Treatments
Assess response and tolerability of past antidepressants
Patient Profile
Consider: Age, pregnancy status, renal/hepatic function, QT prolongation risk
Patient Education Points
Starting Treatment
Explain dose titration and review plan
Onset of Action
Improvement typically takes 2–6 weeks
Duration of Treatment
Minimum 12 months; longer for recurrent depression
Side Effects
Short-Term (1–2 weeks): Nausea, increased anxiety, possible worsening suicidality (temporary)
Long-Term: Weight gain, sexual dysfunction, sedation
Alcohol
Exacerbates depression and counteracts medication effects → avoid
Stopping Antidepressants
Warn against abrupt cessation → taper gradually to avoid withdrawal symptoms (e.g., agitation, dizziness, flu-like symptoms)
Safety in Pregnancy
Avoid paroxetine (congenital malformations); sertraline is preferred
Additional Notes
Address myths about dependency (antidepressants are not addictive)
Incorporate CBT or non-pharmacological therapies in the plan
Monitor for worsening symptoms, especially in:
First month of treatment
Patients <25 years old
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