Serotonin-Noradrenaline Reuptake Inhibitor (SNRI)
Pregnancy: Avoid if possible — neonatal withdrawal syndrome (SSRI discontinuation syndrome-like), pulmonary hypertension (theoretical)
Venlafaxine
Brand names: Efexor XL
Adult dose
Dose: Starting: 37.5–75 mg OD (XL). Increase by 75 mg every 4 weeks as needed. Target: 75–225 mg OD.
Route: Oral (XL capsule — swallow whole)
Frequency: Once daily (XL formulation)
Max: 225 mg/day (depression); 75–225 mg/day (GAD/anxiety)
Higher doses (≥150 mg) have noradrenergic effects. Blood pressure: dose-dependent BP increase. XL capsules must not be opened/crushed. Discontinuation syndrome significant — taper slowly.
Paediatric dose
Route: N/A
Frequency: N/A
Max: Not licensed in children/adolescents
Black box warning in US: increased suicidality in adolescents with depression — not licensed for paediatric use
Dose adjustments
Renal
Reduce daily dose by 25–50% if eGFR <10
Hepatic
Reduce dose by 50% in hepatic impairment
Clinical pearls
- Discontinuation syndrome: among worst of all antidepressants — taper very slowly (reduce by 37.5 mg every 4 weeks minimum; lower reductions if needed)
- Blood pressure: check at baseline and every 3–6 months — dose-dependent rise; discontinue if sustained BP rise
- Nausea: usually resolves after 1–2 weeks — advise patients to persist
- More effective than SSRIs at higher doses due to added noradrenergic mechanism
Contraindications
- MAOIs (within 14 days)
- Severe hepatic impairment
- Uncontrolled hypertension
Side effects
- Nausea (first 2 weeks)
- Sweating
- Dry mouth
- Insomnia
- Hypertension (dose-dependent — monitor BP)
- Tachycardia
- Sexual dysfunction
- Discontinuation syndrome (severe — dizziness, electric shock sensations, crying spells)
Interactions
- MAOIs — serotonin syndrome (absolutely contraindicated)
- Tramadol/triptans — serotonin syndrome risk
- Antihypertensives — reduced effect and BP rise
- Warfarin — may affect INR
Monitoring
- Blood pressure (baseline and periodic)
- ECG (QTc)
- Suicidality (especially early treatment)
- Discontinuation plan before stopping
Reference: BNFc; BNF; NICE NG222 Depression; BAP Antidepressant Guidelines. Verify against your local formulary and the latest BNF before prescribing.
Related
Curated clinical cross-links plus same-class fallbacks.
Calculators
- SMART Risk Score for Recurrent CVD · Cardiovascular Risk
- PCSK9 Inhibitor Eligibility Assessment · Lipid Management
- Immune-Related Adverse Events (irAE) -- GI Toxicity Colitis Grading · Oncology-Related GI
- irAE Hepatitis Grading (CTCAE) · Immunotherapy
- DIPSS — Dynamic International Prognostic Scoring System for Myelofibrosis · Cancer Prognosis
- BALL Score for Relapsed/Refractory CLL · Leukaemia
Pathways
- Acute Behavioural Disturbance / Rapid Tranquillisation · RCEM 2022; RCPsych 2022; NICE NG10
- Self-Harm Presentation · NICE NG225 (2022)
- Capacity Assessment (Mental Capacity Act) · MCA 2005; Code of Practice
- Acute Psychosis Management · NICE CG178 2014
- Depression Management · NICE CG90 2022
- Lithium Therapy Monitoring · NICE CG185 / BNF